Trials side by side
One table, one row per trial arm, so different doses, control groups, and whole trials line up against each other. Each rate is the share of participants in that arm with at least one event of the given severity, always shown next to the number analysed. The context columns (phase, population, size) are here because they explain why two rates differ.
A caution before reading across rows: dose, setting, and screening aren’t normalized across trials yet, so this isn’t a like-for-like ranking. It shows each arm as its own trial reported it, and makes no claim about whether a compound is safe.
440 trial arms with reported safety data
| Compound | Trial · arm | Phase | Population | Analysed | Serious AE | Any non-serious | Deaths |
|---|---|---|---|---|---|---|---|
| Ketamine | A Retrospective Effectiveness Trial of Ketamine-Assisted Psychotherapy in Adult Patients Coping With Mental Health NCT05604794Clients | Phase 4 | Depression, Anxiety | 1806 | 0%0/1806 | 0%0/1806 | 0%0/1806 |
| Ketamine | A Long-term Safety Study of Esketamine Nasal Spray in Treatment-resistant Depression NCT02782104Esketamine Nasal Spray (OP/MA Phase) | Phase 3 | Depressive Disorder, Treatment-Resistant | 1110 | 19%212/1110 | 91%1010/1110 | <1%8/1110 |
| Ketamine | A Long-term, Safety and Efficacy Study of Intranasal Esketamine in Treatment-resistant Depression NCT02497287IND: Intranasal Esketamine + Oral AD | Phase 3 | Treatment-resistant Depression | 779 | 2%17/779 | 75%587/779 | 0%0/779 |
| Ketamine | A Long-term, Safety and Efficacy Study of Intranasal Esketamine in Treatment-resistant Depression NCT02497287OP/MA: Intranasal Esketamine + Oral AD | Phase 3 | Treatment-resistant Depression | 603 | 6%38/603 | 75%454/603 | <1%2/603 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868FU: Intranasal Esketamine + Oral AD | Phase 3 | Depressive Disorder, Treatment-Resistant | 481 | <1%3/481 | 3%14/481 | 0%0/481 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855Follow up: All Participants | Phase 4 | Depressive Disorder, Treatment-Resistant | 476 | <1%1/476 | 2%8/476 | 0%0/477 |
| Ketamine | A Long-term Safety Study of Esketamine Nasal Spray in Treatment-resistant Depression NCT02782104Esketamine Nasal Spray (IND Phase) | Phase 3 | Depressive Disorder, Treatment-Resistant | 458 | 1%5/458 | 69%318/458 | <1%1/458 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868OP: Intranasal Esketamine + Oral AD | Phase 3 | Depressive Disorder, Treatment-Resistant | 455 | 2%11/455 | 61%279/455 | 0%0/455 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868IND: Intranasal Esketamine + Oral AD | Phase 3 | Depressive Disorder, Treatment-Resistant | 437 | 3%13/437 | 70%306/437 | 0%0/437 |
| Ketamine | A Long-term, Safety and Efficacy Study of Intranasal Esketamine in Treatment-resistant Depression NCT02497287FU: Intranasal Esketamine + Oral AD | Phase 3 | Treatment-resistant Depression | 357 | 2%8/357 | 7%24/357 | 0%0/357 |
| Ketamine | A Long-term Comparison of Esketamine Nasal Spray Versus Quetiapine Extended Release, Both in Combination With a Selective Serotonin Reuptake Inhibitor/Serotonin-Norepinephrine Reuptake Inhibitor, in Participants With Treatment Resistant Major Depressive Disorder NCT04338321Quetiapine Extended Release (XR) + Oral AD | Phase 3 | Depressive Disorder, Major | 336 | 5%17/336 | 64%216/336 | <1%1/336 |
| Ketamine | A Long-term Comparison of Esketamine Nasal Spray Versus Quetiapine Extended Release, Both in Combination With a Selective Serotonin Reuptake Inhibitor/Serotonin-Norepinephrine Reuptake Inhibitor, in Participants With Treatment Resistant Major Depressive Disorder NCT04338321Esketamine Nasal Spray + Oral Antidepressant (AD) | Phase 3 | Depressive Disorder, Major | 334 | 6%19/334 | 87%289/334 | <1%1/334 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855DB: Placebo | Phase 4 | Depressive Disorder, Treatment-Resistant | 250 | 1%3/250 | 29%73/250 | 0%0/250 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855OL Treatment: Placebo to Esketamine | Phase 4 | Depressive Disorder, Treatment-Resistant | 237 | 3%6/237 | 62%147/237 | 0%0/237 |
| Ketamine | ELEKT-D: Electroconvulsive Therapy (ECT) vs. Ketamine in Patients With Treatment Resistant Depression (TRD) NCT03113968Ketamine Infusion | Phase 2/Phase 3 | Treatment Resistant Depression, Electroconvulsive Therapy | 195 | 3%5/195 | 16%32/195 | 0%0/195 |
| Ketamine | A Long-Term Extension Study for Participants With Treatment-resistant Major Depressive Disorder Who Are Continuing Esketamine Nasal Spray Treatment NCT04829318Esketamine + Oral AD | Phase 4 | Depressive Disorder, Major | 183 | 6%11/183 | 79%145/183 | <1%1/183 |
| Ketamine | ELEKT-D: Electroconvulsive Therapy (ECT) vs. Ketamine in Patients With Treatment Resistant Depression (TRD) NCT03113968Electroconvulsive Therapy (ECT) | Phase 2/Phase 3 | Treatment Resistant Depression, Electroconvulsive Therapy | 170 | 2%4/170 | 16%27/170 | 0%0/170 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868MA: Intranasal Esketamine + Oral AD | Phase 3 | Depressive Disorder, Treatment-Resistant | 152 | 3%4/152 | 75%114/152 | 0%0/152 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868MA: Oral AD + Intranasal Placebo | Phase 3 | Depressive Disorder, Treatment-Resistant | 145 | <1%1/145 | 31%45/145 | 0%0/145 |
| Ketamine | A Study to Evaluate the Efficacy, Pharmacokinetics, Safety and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT03434041Double-blind: Intranasal Esketamine+ Oral Antidepressant (AD) | Phase 3 | Depressive Disorder, Treatment-Resistant | 126 | 2%3/126 | 94%118/126 | <1%1/126 |
| Ketamine | A Study to Evaluate the Efficacy, Pharmacokinetics, Safety and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT03434041Double-blind: Oral AD + Intranasal Placebo | Phase 3 | Depressive Disorder, Treatment-Resistant | 126 | 2%3/126 | 48%61/126 | 0%0/126 |
| Ketamine | Anhedonia, Development, and Emotions: Phenotyping and Therapeutics NCT05487885Phase 1 | Phase 4 | Depression, Anhedonia | 123 | 0%0/123 | 19%23/123 | 0%0/123 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855DB: Esketamine 84 mg | Phase 4 | Depressive Disorder, Treatment-Resistant | 121 | 2%2/121 | 66%80/121 | 0%0/121 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02417064DB Phase: Intranasal Esk 84 mg + Oral AD | Phase 3 | Treatment-resistant Depression | 116 | 0%0/116 | 79%92/116 | 0%0/116 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02417064DB Phase: Intranasal Esk 56 mg + Oral AD | Phase 3 | Treatment-resistant Depression | 115 | 2%2/115 | 81%93/115 | 0%0/115 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02418585DB Phase: Intranasal Esk + Oral AD | Phase 3 | Treatment-resistant Depression | 115 | <1%1/115 | 78%90/115 | <1%1/115 |
| Ketamine | 54135419SUI3002: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide NCT03097133Esketamine 84 mg + SOC | Phase 3 | Depressive Disorder, Major | 114 | 4%5/114 | 86%98/114 | 0%0/114 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02417064DB Phase: Oral AD + Intranasal Placebo | Phase 3 | Treatment-resistant Depression | 113 | 0%0/113 | 57%64/113 | 0%0/113 |
| Ketamine | 54135419SUI3001: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide NCT03039192Esketamine 84 mg Plus SOC Antidepressant Treatment | Phase 3 | Depressive Disorder, Major | 113 | 4%4/113 | 81%91/113 | 0%0/113 |
| Ketamine | 54135419SUI3002: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide NCT03097133Placebo + Standard of Care (SOC) | Phase 3 | Depressive Disorder, Major | 113 | 5%6/113 | 65%74/113 | 0%0/113 |
| Ketamine | 54135419SUI3001: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide NCT03039192Placebo Plus SOC Antidepressant Treatment | Phase 3 | Depressive Disorder, Major | 112 | 5%6/112 | 59%66/112 | 0%0/112 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02418585DB Phase: Oral AD + Intranasal Placebo | Phase 3 | Treatment-resistant Depression | 109 | <1%1/109 | 49%53/109 | 0%0/109 |
| Ketamine | A Study to Evaluate the Efficacy, Pharmacokinetics, Safety and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT03434041Follow-up: Intranasal Esketamine+ Oral AD | Phase 3 | Depressive Disorder, Treatment-Resistant | 106 | 2%2/106 | 9%10/106 | 0%0/106 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855DB: Esketamine 56 mg | Phase 4 | Depressive Disorder, Treatment-Resistant | 105 | <1%1/105 | 66%69/105 | 0%0/106 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855OL Treatment: Esketamine 84 mg to Esketamine | Phase 4 | Depressive Disorder, Treatment-Resistant | 105 | 0%0/105 | 42%44/105 | 0%0/105 |
| Ketamine | Intravenous Ketamine Plus Neurocognitive Training for Depression NCT03237286Ketamine | Phase 1/Phase 2 | Depression | 103 | 0%0/103 | 99%102/103 | 0%0/103 |
| Ketamine | A Study to Evaluate the Efficacy, Pharmacokinetics, Safety and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT03434041Follow-up: Oral AD + Intranasal Placebo | Phase 3 | Depressive Disorder, Treatment-Resistant | 103 | 2%2/103 | 13%13/103 | 0%0/103 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855OL Treatment: Esketamine 56 mg to Esketamine | Phase 4 | Depressive Disorder, Treatment-Resistant | 99 | 3%3/99 | 49%49/99 | 0%0/99 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868OP_TEP: Oral AD + Intranasal Placebo | Phase 3 | Depressive Disorder, Treatment-Resistant | 86 | 0%0/86 | 47%40/86 | 0%0/86 |
| MDMA | A Multi-Site Open-Label Extension Study of MDMA-Assisted Psychotherapy for PTSD NCT04714359Pre-Treatment MDMA-Assisted Therapy | Phase 3 | PTSD | 85 | 0%0/85 | 60%51/85 | 0%0/85 |
| MDMA | A Multi-Site Open-Label Extension Study of MDMA-Assisted Psychotherapy for PTSD NCT04714359On Day 0, 1, or 2 MDMA-Assisted Therapy | Phase 3 | PTSD | 85 | 0%0/85 | 99%84/85 | 0%0/85 |
| MDMA | A Multi-Site Open-Label Extension Study of MDMA-Assisted Psychotherapy for PTSD NCT04714359Treatment-Emergent Adverse Events MDMA-Assisted Therapy | Phase 3 | PTSD | 85 | 4%3/85 | 99%84/85 | 0%0/85 |
| MDMA | A Multi-Site Open-Label Extension Study of MDMA-Assisted Psychotherapy for PTSD NCT04714359Follow-Up MDMA-Assisted Therapy | Phase 3 | PTSD | 85 | 1%1/85 | 18%15/85 | 0%0/85 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB: Placebo | Phase 2 | Depression | 80 | 1%1/80 | 43%34/80 | 0%0/80 |
| Psilocybin | The Safety and Efficacy of Psilocybin in Participants With Treatment Resistant Depression NCT0377520025 mg COMP360 Psilocybin | Phase 2 | Treatment Resistant Depression | 79 | 6%5/79 | 76%60/79 | 0%0/79 |
| Psilocybin | The Safety and Efficacy of Psilocybin in Participants With Treatment Resistant Depression NCT037752001 mg COMP360 Psilocybin | Phase 2 | Treatment Resistant Depression | 79 | 1%1/79 | 63%50/79 | 0%0/79 |
| Ketamine | The BIO-K Study: A Single-Arm, Open-Label, Biomarker Development Clinical Trial of Ketamine for Non-Psychotic Unipolar Major Depression and Bipolar I or II Depression. NCT03156504Ketamine | Phase 4 | Major Depression, Bipolar I Disorder | 75 | 0%0/75 | 4%3/75 | 0%0/75 |
| Psilocybin | The Safety and Efficacy of Psilocybin in Participants With Treatment Resistant Depression NCT0377520010 mg COMP360 Psilocybin | Phase 2 | Treatment Resistant Depression | 75 | 8%6/75 | 68%51/75 | 0%0/75 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Intranasal Esketamine Plus an Oral Antidepressant in Elderly Participants With Treatment-resistant Depression NCT02422186DB Phase: Intranasal Esketamine + Oral AD (4 Weeks) | Phase 3 | Depressive Disorder, Treatment-Resistant | 72 | 4%3/72 | 61%44/72 | 0%0/72 |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129Total | Phase 2 | Depressive Disorder, Treatment-Resistant | 70 | 7%5/70 | 53%37/70 | 0%0/70 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02417064FU Phase: Oral AD + Intranasal Placebo | Phase 3 | Treatment-resistant Depression | 69 | 1%1/69 | 10%7/69 | 0%0/69 |
| MDMA | Effects of MDMA on Social and Emotional Processing NCT01849419Single Group | NA | Drug Addiction | 65 | 0%0/65 | 0%0/65 | not reported |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Intranasal Esketamine Plus an Oral Antidepressant in Elderly Participants With Treatment-resistant Depression NCT02422186DB Phase: Oral AD + Intranasal Placebo (4 Weeks) | Phase 3 | Depressive Disorder, Treatment-Resistant | 65 | 3%2/65 | 34%22/65 | 0%0/65 |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868FU: Oral AD + Intranasal Placebo | Phase 3 | Depressive Disorder, Treatment-Resistant | 64 | 0%0/64 | 2%1/64 | 0%0/64 |
| Ketamine | miRNAs, Suicide, and Ketamine - Plasma Exosomal microRNAs as Novel Biomarkers for Suicidality and Treatment Outcome NCT02418195MDD With Suicidal Ideation no Attempt | Phase 2 | Major Depressive Disorder | 63 | 2%1/63 | 92%58/63 | 0%0/63 |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819DB: Placebo + Midazolam + SOC | Phase 2 | Depressive Disorder, Major | 63 | 14%9/63 | 90%57/63 | 0%0/63 |
| Ketamine | miRNAs, Suicide, and Ketamine - Plasma Exosomal microRNAs as Novel Biomarkers for Suicidality and Treatment Outcome NCT02418195MDD With Recent Suicide Attempt | Phase 2 | Major Depressive Disorder | 62 | 8%5/62 | 76%47/62 | 0%0/62 |
| Ketamine | miRNAs, Suicide, and Ketamine - Plasma Exosomal microRNAs as Novel Biomarkers for Suicidality and Treatment Outcome NCT02418195MDD Without Suicidal Ideation no Attempt | Phase 2 | Major Depressive Disorder | 61 | 2%1/61 | 98%60/61 | 0%0/61 |
| Ketamine | miRNAs, Suicide, and Ketamine - Plasma Exosomal microRNAs as Novel Biomarkers for Suicidality and Treatment Outcome NCT02418195Healthy Controls | Phase 2 | Major Depressive Disorder | 61 | 0%0/61 | 2%1/61 | 0%0/61 |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819FU Phase: Placebo + Midazolam + SOC | Phase 2 | Depressive Disorder, Major | 59 | 32%19/59 | 81%48/59 | 2%1/59 |
| Psilocybin | Psychopharmacology of Psilocybin in Cancer Patients NCT00465595Low Dose Condition (Group) | Phase 2 | Depressive Symptoms, Anxiety | 56 | 0%0/56 | 18%10/56 | not reported |
| Psilocybin | Psychopharmacology of Psilocybin in Cancer Patients NCT00465595High Dose Condition (Group) | Phase 2 | Depressive Symptoms, Anxiety | 56 | 0%0/56 | 41%23/56 | not reported |
| Ketamine | CAP-Ketamine for Antidepressant Resistant PTSD NCT02655692Placebo | Phase 2 | PTSD, Posttraumatic Stress Disorder | 55 | 0%0/55 | 45%25/55 | 0%0/55 |
| Ketamine | CAP-Ketamine for Antidepressant Resistant PTSD NCT02655692Low Dose Ketamine | Phase 2 | PTSD, Posttraumatic Stress Disorder | 55 | 0%0/55 | 76%42/55 | 0%0/55 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo (Panel A and B: Period 1) | Phase 2 | Treatment Resistant Depressive Disorder | 54 | 0%0/54 | 50%27/54 | not reported |
| Ketamine | A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression NCT02493868MA_TEP: Oral AD + Intranasal Placebo | Phase 3 | Depressive Disorder, Treatment-Resistant | 54 | 2%1/54 | 69%37/54 | 0%0/54 |
| Psilocybin | A Study of Psilocybin for Major Depressive Disorder (MDD) NCT03866174Niacin | Phase 2 | Depressive Disorder, Major | 54 | 0%0/54 | 59%32/54 | 0%0/54 |
| Ketamine | CAP-Ketamine for Antidepressant Resistant PTSD NCT02655692High Dose Ketamine | Phase 2 | PTSD, Posttraumatic Stress Disorder | 53 | 0%0/53 | 72%38/53 | 0%0/53 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB FU: Placebo | Phase 2 | Depression | 53 | 4%2/53 | 13%7/53 | 0%0/53 |
| MDMA | A Multi-Site Phase 3 Study of MDMA-Assisted Psychotherapy for PTSD (MAPP2) NCT04077437MDMA-assisted Therapy | Phase 3 | Posttraumatic Stress Disorder | 53 | 0%0/53 | 100%53/53 | 0%0/53 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02417064FU Phase: Intranasal Esk 84 mg + Oral AD | Phase 3 | Treatment-resistant Depression | 52 | 4%2/52 | 8%4/52 | 0%0/52 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02418585FU Phase: Oral AD + Intranasal Placebo | Phase 3 | Treatment-resistant Depression | 52 | 0%0/52 | 12%6/52 | 0%0/52 |
| Psilocybin | Psilocybin-Assisted Therapy for the Treatment of Cancer-Related Anxiety in Patients With Metastatic Cancer NCT05847686Treatment (Psilocybin, Therapy) | Phase 1/Phase 2 | Hematopoietic and Lymphatic System Neoplasm, Metastatic Malignant Solid Neoplasm | 52 | 6%3/52 | 58%30/52 | 4%2/52 |
| Ketamine | Intravenous Ketamine Plus Neurocognitive Training for Depression NCT03237286Saline | Phase 1/Phase 2 | Depression | 51 | 0%0/51 | 75%38/51 | 0%0/51 |
| MDMA | A Multi-Site Phase 3 Study of MDMA-Assisted Psychotherapy for PTSD (MAPP2) NCT04077437Placebo With Therapy | Phase 3 | Posttraumatic Stress Disorder | 51 | 0%0/51 | 96%49/51 | 0%0/51 |
| Psilocybin | A Study of Psilocybin for Major Depressive Disorder (MDD) NCT03866174Psilocybin | Phase 2 | Depressive Disorder, Major | 50 | 0%0/50 | 86%43/50 | 0%0/50 |
| Ketamine | Anhedonia, Development, and Emotions: Phenotyping and Therapeutics NCT05487885TMS and PAT | Phase 4 | Depression, Anhedonia | 50 | 0%0/50 | 6%3/50 | 0%0/50 |
| Psilocybin | A Double-Blind Trial of Psilocybin-Assisted Treatment of Alcohol Dependence NCT02061293Psilocybin | Phase 2 | Alcohol Dependence | 48 | 0%0/48 | 77%37/48 | 0%0/48 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318Open-Label (OL): Flexible Esketamine | Phase 2 | Depression | 48 | 2%1/48 | 98%47/48 | 0%0/48 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318OL FU: Flexible Esketamine | Phase 2 | Depression | 48 | 4%2/48 | 6%3/48 | 0%0/48 |
| Ketamine | Optimization of IV Ketamine for Treatment Resistant Depression NCT00768430Ketamine | Phase 2 | Major Depressive Disorder (MDD), Treatment Resistant Depression (TRD) | 47 | 4%2/47 | 100%47/47 | not reported |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02417064FU Phase: Intranasal Esk 56 mg + Oral AD | Phase 3 | Treatment-resistant Depression | 47 | 4%2/47 | 15%7/47 | 0%0/47 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine/Esketamine/Open Label Esketamine (Panel A and B) | Phase 2 | Treatment Resistant Depressive Disorder | 46 | 2%1/46 | 85%39/46 | not reported |
| Ketamine | Study on the Use of Low Dose Ketamine After Gastric Bypass and Gastrectomy NCT02452060Treatment/Placebo | Phase 2/Phase 3 | Pain, Postoperative Depression | 46 | 0%0/46 | 20%9/46 | 0%0/46 |
| MDMA | A Multi-Site Phase 3 Study of MDMA-Assisted Psychotherapy for PTSD (MAPP1) NCT03537014MDMA-assisted Therapy | Phase 3 | Posttraumatic Stress Disorder | 46 | 0%0/46 | 100%46/46 | 0%0/46 |
| Psilocybin | A Double-Blind Trial of Psilocybin-Assisted Treatment of Alcohol Dependence NCT02061293Diphenhydramine | Phase 2 | Alcohol Dependence | 45 | 4%2/45 | 64%29/45 | 0%0/45 |
| Ketamine | Study on the Use of Low Dose Ketamine After Gastric Bypass and Gastrectomy NCT02452060Treatment | Phase 2/Phase 3 | Pain, Postoperative Depression | 44 | 0%0/44 | 16%7/44 | 0%0/44 |
| MDMA | A Multi-Site Phase 3 Study of MDMA-Assisted Psychotherapy for PTSD (MAPP1) NCT03537014Placebo With Therapy | Phase 3 | Posttraumatic Stress Disorder | 44 | 5%2/44 | 100%44/44 | 0%0/44 |
| Psilocybin | Psilocybin-facilitated Smoking Cessation Treatment: A Pilot Study NCT01943994Psilocybin-assisted Treatment | NA | Nicotine Dependence | 42 | 0%0/42 | 88%37/42 | 0%0/42 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 84 mg: Follow up Phase | Phase 2 | Treatment Resistant Depressive Disorder | 42 | 2%1/42 | 17%7/42 | not reported |
| Ketamine | Elucidating the Neurocircuitry of Irritability With High-Field Neuroimaging to Identify Novel Therapeutic Targets NCT05046184Healthy Control | Phase 2 | Major Depressive Disorder, Healthy Controls | 42 | 0%0/42 | 2%1/42 | 0%0/42 |
| Ketamine | Rapid Antidepressant Effects of Ketamine in Major Depression NCT00088699MDD: Ketamine | Phase 1/Phase 2 | Depression, Mood Disorders | 41 | 0%0/41 | 88%36/41 | 0%0/41 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318Double Blind (DB): Esketamine 28 mg | Phase 2 | Depression | 41 | 2%1/41 | 80%33/41 | 0%0/41 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB: Esketamine 56 mg | Phase 2 | Depression | 41 | 0%0/41 | 95%39/41 | 0%0/41 |
| Ketamine | Ketamine in the Treatment of Suicidal Depression NCT01700829Midazolam | Phase 4 | Major Depressive Disorder, Suicidal Ideation | 40 | 10%4/40 | 30%12/40 | 0%0/40 |
| Ketamine | Ketamine in the Treatment of Suicidal Depression NCT01700829Ketamine | Phase 4 | Major Depressive Disorder, Suicidal Ideation | 40 | 13%5/40 | 25%10/40 | 0%0/40 |
| Psilocybin | Psilocybin-facilitated Smoking Cessation Treatment: A Pilot Study NCT01943994Nicotine Replacement Therapy (NRT) | NA | Nicotine Dependence | 40 | 3%1/40 | 78%31/40 | 0%0/40 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB: Esketamine 84 mg | Phase 2 | Depression | 40 | 3%1/40 | 98%39/40 | 0%0/40 |
| LSD | A Dose-Finding Study of MM120 (LSD D-Tartrate) for the Treatment of Anxiety Symptoms NCT05407064Arm 3- 50 μg MM120 | Phase 2 | Anxiety Generalized | 40 | 3%1/40 | 90%36/40 | 0%0/40 |
| LSD | A Dose-Finding Study of MM120 (LSD D-Tartrate) for the Treatment of Anxiety Symptoms NCT05407064Arm 4- 100 μg MM120 | Phase 2 | Anxiety Generalized | 40 | 0%0/40 | 98%39/40 | 0%0/40 |
| LSD | A Dose-Finding Study of MM120 (LSD D-Tartrate) for the Treatment of Anxiety Symptoms NCT05407064Arm 5- 200 μg MM120 | Phase 2 | Anxiety Generalized | 40 | 0%0/40 | 100%40/40 | 0%0/40 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 56 mg: Follow up Phase | Phase 2 | Treatment Resistant Depressive Disorder | 39 | 3%1/39 | 26%10/39 | not reported |
| LSD | A Dose-Finding Study of MM120 (LSD D-Tartrate) for the Treatment of Anxiety Symptoms NCT05407064Arm 1- Placebo | Phase 2 | Anxiety Generalized | 39 | 0%0/39 | 56%22/39 | 0%0/39 |
| LSD | A Dose-Finding Study of MM120 (LSD D-Tartrate) for the Treatment of Anxiety Symptoms NCT05407064Arm 2- 25 μg MM120 | Phase 2 | Anxiety Generalized | 39 | 0%0/39 | 77%30/39 | 0%0/39 |
| Ketamine | Rapid Antidepressant Effects of Ketamine in Major Depression NCT00088699MDD: Placebo | Phase 1/Phase 2 | Depression, Mood Disorders | 38 | 0%0/38 | 42%16/38 | 0%0/38 |
| Ketamine | Ketamine as a Rapid Treatment for Post-traumatic Stress Disorder (PTSD) NCT00749203Ketamine | Phase 2 | Stress Disorders, Post-Traumatic, PTSD | 38 | 87%33/38 | 0%0/38 | 0%0/38 |
| Ketamine | Ketamine in the Treatment of Depression NCT01558063All Subjects | Phase 2 | Major Depressive Disorder | 38 | 11%4/38 | 0%0/38 | 0%0/38 |
| Ketamine | PET Imaging of mGLuR5 With Drug Challenge NCT01691092Ketamine | NA | Major Depressive Disorder, Post-Traumatic Stress Disorder (PTSD) | 38 | 3%1/38 | 0%0/38 | not reported |
| Ketamine | Ketamine-enhanced Prolonged Exposure Therapy in PTSD NCT04560660Ketamine and Prolonged Exposure (PE) | Phase 2 | PTSD | 37 | 3%1/37 | 89%33/37 | 0%0/37 |
| Ketamine | Ketamine-enhanced Prolonged Exposure Therapy in PTSD NCT04560660Midazolam and Prolonged Exposure (PE) | Phase 2 | PTSD | 36 | 3%1/36 | 94%34/36 | 0%0/36 |
| Ketamine | A Double-blind Study to Assess the Efficacy and Safety of Intranasal Esketamine for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Participants Who Are Assessed to be at Imminent Risk for Suicide NCT02133001Double Blind (Day 1-25): Esketamine 84 mg | Phase 2 | Major Depressive Disorder | 35 | 11%4/35 | 86%30/35 | not reported |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Participants With Treatment-resistant Depression NCT02418585FU Phase: Intranasal Esk + Oral AD | Phase 3 | Treatment-resistant Depression | 34 | 3%1/34 | 21%7/34 | 0%0/34 |
| MDMA | Open Label Multi-Site Study of Safety and Effects of MDMA-assisted Therapy for Treatment of PTSD NCT03282123MDMA-assisted Psychotherapy | Phase 2 | PTSD | 33 | 3%1/33 | 100%33/33 | 0%0/33 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 56 mg (Panel A and B: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 32 | 0%0/32 | 81%26/32 | not reported |
| Ketamine | Ketamine as a Rapid Treatment for Post-traumatic Stress Disorder (PTSD) NCT00749203Midazolam | Phase 2 | Stress Disorders, Post-Traumatic, PTSD | 31 | 100%31/31 | 0%0/31 | 0%0/31 |
| Ketamine | A Double-blind Study to Assess the Efficacy and Safety of Intranasal Esketamine for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Participants Who Are Assessed to be at Imminent Risk for Suicide NCT02133001Double Blind (Day 1-25): Placebo | Phase 2 | Major Depressive Disorder | 31 | 0%0/31 | 81%25/31 | not reported |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819DB: Esketamine 56 mg + Placebo + SOC | Phase 2 | Depressive Disorder, Major | 31 | 23%7/31 | 97%30/31 | 0%0/31 |
| Ketamine | Elucidating the Neurocircuitry of Irritability With High-Field Neuroimaging to Identify Novel Therapeutic Targets NCT05046184MDD: Ketamine | Phase 2 | Major Depressive Disorder, Healthy Controls | 31 | 0%0/31 | 35%11/31 | 0%0/31 |
| Ketamine | Elucidating the Neurocircuitry of Irritability With High-Field Neuroimaging to Identify Novel Therapeutic Targets NCT05046184MDD: Midazolam | Phase 2 | Major Depressive Disorder, Healthy Controls | 31 | 0%0/31 | 16%5/31 | 0%0/31 |
| Psilocybin | Psilocybin vs Escitalopram for Major Depressive Disorder: Comparative Mechanisms NCT03429075Psilocybin | Phase 2 | Depressive Disorder, Major | 30 | 0%0/30 | 87%26/30 | 0%0/30 |
| Psilocybin | Psilocybin Cancer Anxiety Study NCT00957359Psilocybin | EARLY_Phase 1 | Cancer | 29 | 0%0/29 | 3%1/29 | 0%0/29 |
| Psilocybin | Psilocybin Cancer Anxiety Study NCT00957359Niacin | EARLY_Phase 1 | Cancer | 29 | 0%0/29 | 0%0/29 | 0%0/29 |
| Ketamine | Efficacy of Repeated Ketamine Infusions for Treatment-resistant Depression NCT02360280Single Ketamine Infusion Preceded by 5 Midazolam Infusions | Phase 2 | Treatment-resistant Depression | 29 | 3%1/29 | 28%8/29 | 0%0/29 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB FU: Esketamine 56 mg | Phase 2 | Depression | 29 | 0%0/29 | 10%3/29 | 0%0/29 |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819DB: Esketamine 28 mg + Placebo + SOC | Phase 2 | Depressive Disorder, Major | 29 | 14%4/29 | 90%26/29 | 0%0/29 |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819FU Phase: Esketamine 28 mg + Placebo + SOC | Phase 2 | Depressive Disorder, Major | 29 | 34%10/29 | 72%21/29 | 0%0/29 |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819FU Phase: Esketamine 56 mg + Placebo + SOC | Phase 2 | Depressive Disorder, Major | 29 | 28%8/29 | 66%19/29 | 0%0/29 |
| Psilocybin | Psilocybin vs Escitalopram for Major Depressive Disorder: Comparative Mechanisms NCT03429075Escitalopram | Phase 2 | Depressive Disorder, Major | 29 | 0%0/29 | 83%24/29 | 0%0/29 |
| Ketamine | Ketamine Versus Midazolam for Recurrence of Suicidality in Adolescents NCT04592809Ketamine | Phase 3 | Suicide, Attempted, Suicide and Depression | 28 | 18%5/28 | 100%28/28 | 0%0/28 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo/Esketamine/Open Label Esketamine (Panel A and B) | Phase 2 | Treatment Resistant Depressive Disorder | 27 | 0%0/27 | 81%22/27 | not reported |
| Ketamine | A Double-blind Study to Assess the Efficacy and Safety of Intranasal Esketamine for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Participants Who Are Assessed to be at Imminent Risk for Suicide NCT02133001Follow Up Phase (Day 26-81): Esketamine 84 mg | Phase 2 | Major Depressive Disorder | 27 | 4%1/27 | 41%11/27 | not reported |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB Follow Up (FU): Esketamine 28 mg | Phase 2 | Depression | 27 | 0%0/27 | 11%3/27 | 0%0/27 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318PT Phase: Placebo | Phase 2 | Depression | 27 | 0%0/27 | 26%7/27 | 0%0/27 |
| LSD | Safety and Efficacy of Low Dose MM120 for ADHD Proof of Concept Trial NCT05200936Arm 2- MM120 | Phase 2 | ADHD, Attention Deficit Disorder | 27 | 0%0/27 | 78%21/27 | 0%0/27 |
| Ketamine | Research Study for Major Depressive Disorder: Investigation of Glutamate Medications NCT00419003Ketamine | Phase 4 | Major Depression | 26 | 0%0/26 | 100%26/26 | not reported |
| Psilocybin | Psilocybin-facilitated Smoking Cessation Treatment: A Pilot Study NCT01943994Cross-over to Psilocybin-assisted Treatment | NA | Nicotine Dependence | 26 | 4%1/26 | 96%25/26 | 0%0/26 |
| Ketamine | A Study of Brexpiprazole Plus Ketamine in Treatment-Resistant Depression (TRD) NCT03149991Placebo | Phase 4 | Depression | 26 | 0%0/26 | 69%18/26 | 0%0/26 |
| Ketamine | Postpartum Perineal Pain After Obstetric Anal Sphincter Injuries NCT03470675Epidural Morphine 3 mg + IV Saline | Phase 4 | Pain, Postpartum Depression | 26 | 0%0/26 | 54%14/26 | 0%0/26 |
| LSD | Safety and Efficacy of Low Dose MM120 for ADHD Proof of Concept Trial NCT05200936Arm 1- Placebo | Phase 2 | ADHD, Attention Deficit Disorder | 26 | 0%0/26 | 88%23/26 | 0%0/26 |
| Ketamine | Optimization of IV Ketamine for Treatment Resistant Depression NCT00768430Midazolam | Phase 2 | Major Depressive Disorder (MDD), Treatment Resistant Depression (TRD) | 25 | 0%0/25 | 100%25/25 | not reported |
| Ketamine | Alternative Sedation During Bronchoscopy NCT01158820Placebo | Phase 4 | Sedation | 25 | 0%0/25 | 0%0/25 | 0%0/25 |
| Ketamine | Alternative Sedation During Bronchoscopy NCT01158820Dexmedetomidine and Ketamine | Phase 4 | Sedation | 25 | 0%0/25 | 0%0/25 | 0%0/25 |
| Ketamine | Efficacy of Repeated Ketamine Infusions for Treatment-resistant Depression NCT02360280Six Ketamine Infusions | Phase 2 | Treatment-resistant Depression | 25 | 4%1/25 | 68%17/25 | 0%0/25 |
| Ketamine | Ketamine for Reduction of Alcoholic Relapse NCT02649231Placebo+Education | Phase 2 | Primary Alcohol Use Disorder | 25 | 4%1/25 | 68%17/25 | 0%0/25 |
| Ketamine | A Study of Brexpiprazole Plus Ketamine in Treatment-Resistant Depression (TRD) NCT03149991Brexpiprazole | Phase 4 | Depression | 25 | 0%0/25 | 68%17/25 | 0%0/25 |
| Ketamine | Postpartum Perineal Pain After Obstetric Anal Sphincter Injuries NCT03470675Epidural Morphine 3 mg + IV Ketamine 0.3 mg/kg | Phase 4 | Pain, Postpartum Depression | 25 | 0%0/25 | 52%13/25 | 0%0/25 |
| Ketamine | Rapid Antidepressant Effects of Ketamine in Major Depression NCT00088699Healthy Volunteer: Ketamine | Phase 1/Phase 2 | Depression, Mood Disorders | 24 | 0%0/24 | 100%24/24 | 0%0/24 |
| Ketamine | Ketamine for Reduction of Alcoholic Relapse NCT02649231Ketamine+Psychological Therapy | Phase 2 | Primary Alcohol Use Disorder | 24 | 0%0/24 | 54%13/24 | 0%0/24 |
| Ketamine | Ketamine for Reduction of Alcoholic Relapse NCT02649231Ketamine+Education | Phase 2 | Primary Alcohol Use Disorder | 24 | 0%0/24 | 71%17/24 | 0%0/24 |
| Psilocybin | Effects of Psilocybin in Major Depressive Disorder NCT03181529Session #1 Through 1-week Post-session #1 Follow-up | Phase 2 | Major Depressive Disorder | 24 | 0%0/24 | 38%9/24 | 0%0/24 |
| Psilocybin | Effects of Psilocybin in Major Depressive Disorder NCT03181529Session #2 Through 1-week Post-session #2 Follow-up | Phase 2 | Major Depressive Disorder | 24 | 0%0/24 | 46%11/24 | 0%0/24 |
| Ketamine | Anhedonia, Development, and Emotions: Phenotyping and Therapeutics NCT05487885Ketamine | Phase 4 | Depression, Anhedonia | 24 | 0%0/24 | 17%4/24 | 0%0/24 |
| Ketamine | Rapid Antidepressant Effects of Ketamine in Major Depression NCT00088699Healthy Volunteer: Placebo | Phase 1/Phase 2 | Depression, Mood Disorders | 23 | 0%0/23 | 35%8/23 | 0%0/23 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo (Panel A and B: Period 2) QIDS >=11 Participants | Phase 2 | Treatment Resistant Depressive Disorder | 23 | 4%1/23 | 65%15/23 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo (Panel A and Panel B: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 23 | 4%1/23 | 52%12/23 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo/Placebo/Open Label Esketamine (Panel A and B) | Phase 2 | Treatment Resistant Depressive Disorder | 23 | 0%0/23 | 100%23/23 | not reported |
| Ketamine | Ketamine for Reduction of Alcoholic Relapse NCT02649231Placebo+Psychological Therapy | Phase 2 | Primary Alcohol Use Disorder | 23 | 9%2/23 | 70%16/23 | 0%0/23 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318DB FU: Esketamine 84 mg | Phase 2 | Depression | 23 | 4%1/23 | 13%3/23 | 0%0/23 |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819DB: Esketamine 84 mg + Placebo + SOC | Phase 2 | Depressive Disorder, Major | 23 | 4%1/23 | 100%23/23 | 0%0/23 |
| Ketamine | Ketamine for Older Adults Pilot NCT04504175Acute | Phase 4 | Treatment Resistant Depression, Refractory Depression | 23 | 0%0/23 | 17%4/23 | 0%0/23 |
| Ketamine | Double-Blind, Placebo-Controlled Trial of Ketamine Therapy in Treatment-Resistant Depression (TRD) NCT01920555Ketamine 0.5mg | Phase 2 | Treatment Resistant Depression | 22 | 0%0/22 | 64%14/22 | 0%0/22 |
| Ketamine | A Double-blind Study to Assess the Efficacy and Safety of Intranasal Esketamine for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Participants Who Are Assessed to be at Imminent Risk for Suicide NCT02133001Follow Up Phase (Day 26-81): Placebo | Phase 2 | Major Depressive Disorder | 22 | 23%5/22 | 27%6/22 | not reported |
| MDMA | Effects of Drugs on Responses to Brain and Emotional Processes NCT04053036Placebo | EARLY_Phase 1 | Autism Spectrum Disorder, Healthy | 22 | 0%0/22 | 0%0/22 | 0%0/22 |
| MDMA | Effects of Drugs on Responses to Brain and Emotional Processes NCT04053036MDMA | EARLY_Phase 1 | Autism Spectrum Disorder, Healthy | 22 | 0%0/22 | 0%0/22 | 0%0/22 |
| Ketamine | Ketamine Versus Midazolam for Recurrence of Suicidality in Adolescents NCT04592809Midazolam | Phase 3 | Suicide, Attempted, Suicide and Depression | 22 | 32%7/22 | 100%22/22 | 0%0/22 |
| Ketamine | Ketamine + Mindfulness for Depression NCT05168735Intravenous Ketamine + Mindfulness Exercises | Phase 1/Phase 2 | Depression, Unipolar | 22 | 0%0/22 | 100%22/22 | 0%0/22 |
| Psilocybin | The Safety and Tolerability of COMP360 in Participants With Post-traumatic Stress Disorder NCT05312151COMP360 Psilocybin | Phase 2 | Post Traumatic Stress Disorder | 22 | 0%0/22 | 100%22/22 | 0%0/22 |
| Ketamine | Ketamine Anesthesia in Electroconvulsive Therapy NCT01367119Ketamine | NA | Depression | 21 | 0%0/21 | 0%0/21 | not reported |
| Ketamine | Study to Evaluate the Efficacy and Safety of 3 Fixed Doses of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Pediatric Participants Assessed to be at Imminent Risk for Suicide NCT03185819FU Phase: Esketamine 84 mg + Placebo + SOC | Phase 2 | Depressive Disorder, Major | 21 | 33%7/21 | 67%14/21 | 0%0/21 |
| MDMA | Open Label Study of MDMA-assisted Psychotherapy for Treatment of PTSD With Optional fMRI Sub-Study NCT04030169Experimental: MDMA-assisted Psychotherapy | Phase 2 | PTSD | 21 | 10%2/21 | 100%21/21 | 0%0/21 |
| Ketamine | Ketamine + Mindfulness for Depression NCT05168735Intravenous Ketamine + Academic Exercises | Phase 1/Phase 2 | Depression, Unipolar | 21 | 0%0/21 | 100%21/21 | 0%0/21 |
| Ketamine | Double-Blind, Placebo-Controlled Trial of Ketamine Therapy in Treatment-Resistant Depression (TRD) NCT01920555Ketamine 0.2mg | Phase 2 | Treatment Resistant Depression | 20 | 5%1/20 | 90%18/20 | 0%0/20 |
| Ketamine | Double-Blind, Placebo-Controlled Trial of Ketamine Therapy in Treatment-Resistant Depression (TRD) NCT01920555Ketamine 1.0mg | Phase 2 | Treatment Resistant Depression | 20 | 0%0/20 | 85%17/20 | 0%0/20 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 56 mg (Panel A and B: Period 1) | Phase 2 | Treatment Resistant Depressive Disorder | 20 | 0%0/20 | 90%18/20 | not reported |
| Psilocybin | Psilocybin-facilitated Treatment for Cocaine Use NCT02037126Psilocybin Administration | Phase 2 | Cocaine-Related Disorders | 20 | 0%0/20 | 65%13/20 | 0%0/20 |
| Psilocybin | Psilocybin-facilitated Treatment for Cocaine Use NCT02037126Diphenhydramine Administration | Phase 2 | Cocaine-Related Disorders | 20 | 0%0/20 | 10%2/20 | 0%0/20 |
| Ketamine | Ketamine for the Rapid Treatment of Major Depressive Disorder and Alcohol Use Disorder NCT02461927Ketamine + Naltrexone | Phase 1/Phase 2 | Major Depressive Disorder, Alcohol Use Disorder | 20 | 0%0/20 | 70%14/20 | 0%0/20 |
| Ketamine | Examining the Impact of Sirolimus on Ketamine's Antidepressant Effects NCT02487485Ketamine + Sirolimus | Phase 2 | Depression | 20 | 0%0/20 | 30%6/20 | 0%0/20 |
| Ketamine | Examining the Impact of Sirolimus on Ketamine's Antidepressant Effects NCT02487485Ketamine + Placebo | Phase 2 | Depression | 20 | 0%0/20 | 30%6/20 | 0%0/20 |
| MDMA | Effects of MDMA on Emotional and Social Memories NCT03050541Healthy Adult Volunteers-Oral MDMA at Memory Encoding | NA | Healthy | 20 | 0%0/20 | 0%0/20 | not reported |
| MDMA | Effects of MDMA on Emotional and Social Memories NCT03050541Healthy Adult Volunteers-Oral MDMA at Memory Retrievial | NA | Healthy | 20 | 0%0/20 | 0%0/20 | not reported |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129Placebo Weekly | Phase 2 | Depressive Disorder, Treatment-Resistant | 20 | 5%1/20 | 25%5/20 | 0%0/20 |
| Ketamine | Intraoperative Ketamine Versus Saline in Depressed Patients Undergoing Anesthesia for Non-cardiac Surgery NCT03861988Double Blind Ketamine | Phase 4 | Major Depressive Disorder, Surgery | 20 | 5%1/20 | 35%7/20 | 5%1/20 |
| Ketamine | Intraoperative Ketamine Versus Saline in Depressed Patients Undergoing Anesthesia for Non-cardiac Surgery NCT03861988Double Blind Placebo | Phase 4 | Major Depressive Disorder, Surgery | 20 | 10%2/20 | 30%6/20 | 0%0/20 |
| Ketamine | Intranasal Ketamine in Treatment-Resistant Depression NCT01304147Ketamine | NA | Major Depressive Disorder | 19 | 0%0/19 | 100%19/19 | not reported |
| Ketamine | Intranasal Ketamine in Treatment-Resistant Depression NCT01304147Placebo | NA | Major Depressive Disorder | 19 | 0%0/19 | 100%19/19 | not reported |
| Ketamine | Double-Blind, Placebo-Controlled Trial of Ketamine Therapy in Treatment-Resistant Depression (TRD) NCT01920555Midazolam (Active Placebo) | Phase 2 | Treatment Resistant Depression | 19 | 0%0/19 | 53%10/19 | 0%0/19 |
| Ketamine | Ketamine for the Rapid Treatment of Major Depressive Disorder and Alcohol Use Disorder NCT02461927Ketamine + Placebo | Phase 1/Phase 2 | Major Depressive Disorder, Alcohol Use Disorder | 19 | 0%0/19 | 58%11/19 | 0%0/19 |
| Ketamine | Ketamine for the Rapid Treatment of Major Depressive Disorder and Alcohol Use Disorder NCT02461927Placebo (Psychoactive Placebo Midazolam) + Placebo | Phase 1/Phase 2 | Major Depressive Disorder, Alcohol Use Disorder | 19 | 0%0/19 | 74%14/19 | 0%0/19 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005Placebo | Phase 1 | Major Depressive Disorder | 19 | 0%0/19 | 26%5/19 | 0%0/19 |
| Psilocybin | The Safety and Efficacy Of Psilocybin as an Adjunctive Therapy in Participants With Treatment Resistant Depression NCT0473986525 mg COMP360 Psilocybin | Phase 2 | Treatment Resistant Depression | 19 | 0%0/19 | 63%12/19 | 0%0/19 |
| Ketamine | A Study of Ketamine in Patients With Treatment-resistant Depression NCT01627782Ketamine: 2 Times Per Week | Phase 2 | Major Depressive Disorder | 18 | 11%2/18 | 83%15/18 | not reported |
| Ketamine | Ketamine Plus Lithium in Treatment-Resistant Depression NCT01880593Ketamine and Lithium | Phase 2 | Depression | 18 | 0%0/18 | 83%15/18 | 0%0/18 |
| Ketamine | Double-Blind, Placebo-Controlled Trial of Ketamine Therapy in Treatment-Resistant Depression (TRD) NCT01920555Ketamine 0.1mg | Phase 2 | Treatment Resistant Depression | 18 | 0%0/18 | 94%17/18 | 0%0/18 |
| Psilocybin | Psilocybin-assisted Group Therapy for Demoralization in Long-term AIDS Survivors NCT02950467Group Therapy Plus Psilocybin | Phase 1 | Distress, Depression | 18 | 17%3/18 | 100%18/18 | 0%0/18 |
| Ketamine | Ketamine Anesthesia in Electroconvulsive Therapy NCT01367119Methohexital | NA | Depression | 17 | 0%0/17 | 0%0/17 | not reported |
| Ketamine | A Study of Ketamine in Patients With Treatment-resistant Depression NCT01627782Ketamine: 3 Times Per Week | Phase 2 | Major Depressive Disorder | 17 | 0%0/17 | 76%13/17 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 84 mg (Panel A: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 17 | 0%0/17 | 71%12/17 | not reported |
| Ketamine | Ketamine Infusion for Adolescent Depression and Anxiety NCT02579928Ketamine | Phase 4 | Major Depressive Disorder, Anxiety Disorder | 17 | 0%0/17 | 88%15/17 | 0%0/17 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318PT Phase: Esketamine 84 mg | Phase 2 | Depression | 17 | 0%0/17 | 35%6/17 | 0%0/17 |
| Ketamine | Trial of the Rapid Antisuicidal Effects of Intranasal Ketamine in Comorbid Depression and Alcohol Abuse NCT03539887Intranasal Ketamine | Phase 3 | Suicidal Ideation, Depression | 17 | 0%0/17 | 71%12/17 | 0%0/17 |
| Ketamine | Inpatient Single Dose Interventions for Alcohol Use Disorder NCT04562779Linkage | EARLY_Phase 1 | Alcohol Use Disorder, Severe | 17 | 0%0/17 | 35%6/17 | 0%0/17 |
| Ketamine | A Study of Ketamine in Patients With Treatment-resistant Depression NCT01627782Placebo: 2 Times Per Week | Phase 2 | Major Depressive Disorder | 16 | 0%0/16 | 56%9/16 | not reported |
| Ketamine | A Study of Ketamine in Patients With Treatment-resistant Depression NCT01627782Placebo: 3 Times Per Week | Phase 2 | Major Depressive Disorder | 16 | 0%0/16 | 50%8/16 | not reported |
| Ketamine | Ketamine Plus Lithium in Treatment-Resistant Depression NCT01880593Ketamine and Placebo | Phase 2 | Depression | 16 | 0%0/16 | 75%12/16 | 0%0/16 |
| Ketamine | Ketamine as an Augmentation Strategy for Electroconvulsive Therapy (ECT) in Depression NCT01881763Ketamine | Phase 4 | Unipolar Depression, Bipolar Depression | 16 | 0%0/16 | 0%0/16 | 0%0/16 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 14 mg (Panel B: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 16 | 0%0/16 | 69%11/16 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 28 mg (Panel A: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 16 | 0%0/16 | 50%8/16 | not reported |
| Ketamine | Ketamine for Depression: An MRI Study NCT02544607Ketamine | Phase 4 | Depression, Anxious Depression | 16 | 0%0/16 | 6%1/16 | 0%0/16 |
| Ketamine | Ketamine Infusion for Adolescent Depression and Anxiety NCT02579928Midazolam | Phase 4 | Major Depressive Disorder, Anxiety Disorder | 16 | 0%0/16 | 81%13/16 | 0%0/16 |
| Psilocybin | Psilocybin-assisted CBT for Depression NCT05227612Psilocybin-assisted Cognitive Behavioral Therapy (PACBT) | Phase 1 | Major Depressive Disorder | 16 | 0%0/16 | 94%15/16 | 0%0/16 |
| Ketamine | Ketamine for Postoperative Avoidance of Depressive Symptoms: The K-PASS Feasibility Trial NCT05233566Ketamine Arm | Phase 3 | Postoperative Depression | 16 | 13%2/16 | 0%0/16 | 0%0/16 |
| Ketamine | Ketamine for Postoperative Avoidance of Depressive Symptoms: The K-PASS Feasibility Trial NCT05233566Control Arm | Phase 3 | Postoperative Depression | 16 | 31%5/16 | 19%3/16 | 6%1/16 |
| MDMA | MDMA-Assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00090064MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 15 | 13%2/15 | 87%13/15 | 0%0/15 |
| MDMA | MDMA-Assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00090064SRRs: MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 15 | 0%0/15 | 100%15/15 | 0%0/15 |
| Ketamine | Ketamine as an Augmentation Strategy for Electroconvulsive Therapy (ECT) in Depression NCT01881763Methohexital | Phase 4 | Unipolar Depression, Bipolar Depression | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Ketamine | Ketamine as a Treatment for Post-Traumatic Stress Disorder (PTSD) NCT02397889Experimental Ketamine Group | Phase 2/Phase 3 | Posttraumatic Stress Disorder (PTSD) | 15 | 0%0/15 | 100%15/15 | 0%0/15 |
| Ketamine | Ketamine as a Treatment for Post-Traumatic Stress Disorder (PTSD) NCT02397889Active Control Midazolam Group | Phase 2/Phase 3 | Posttraumatic Stress Disorder (PTSD) | 15 | 0%0/15 | 100%15/15 | 0%0/15 |
| Ketamine | Cognitive Recovery After Electroconvulsive Therapy and General Anesthesia NCT02761330Ketamine +ECT | NA | Depression, Delirium | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Ketamine | Cognitive Recovery After Electroconvulsive Therapy and General Anesthesia NCT02761330Etomidate +ECT | NA | Depression, Delirium | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Ketamine | Cognitive Recovery After Electroconvulsive Therapy and General Anesthesia NCT02761330Ketamine Sham | NA | Depression, Delirium | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Ayahuasca | Antidepressant Effects of Ayahuasca: a Randomized Placebo Controlled Trial in Treatment Resistant Depression NCT02914769Placebo | Phase 1/Phase 2 | Major Depression | 15 | 0%0/15 | 27%4/15 | not reported |
| Ketamine | Ketamine for Older Adults Pilot NCT04504175Continuation | Phase 4 | Treatment Resistant Depression, Refractory Depression | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Ketamine | Repeated Neurocognitive Measurements in Depressed Patients NCT04916548Intravenous Ketamine | Phase 1/Phase 2 | Depression, Unipolar | 15 | 0%0/15 | 93%14/15 | 0%0/15 |
| Psilocybin | Pilot Study of Psilocybin-Assisted Therapy for Demoralization in Patients Receiving Hospice Care NCT04950608Psilocybin- Single Arm | Phase 2 | Hospice, Psilocybin | 15 | 67%10/15 | 87%13/15 | 60%9/15 |
| Psilocybin | Frontline Clinician Psilocybin Study NCT05163496Psilocybin Arm | Phase 3 | Burnout, Caregiver, Burnout, Professional | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Psilocybin | Frontline Clinician Psilocybin Study NCT05163496Placebo | Phase 3 | Burnout, Caregiver, Burnout, Professional | 15 | 0%0/15 | 0%0/15 | 0%0/15 |
| Ketamine | Ketamine Infusion for Treatment-resistant Major Depressive Disorder NCT01582945Ketamine IV | NA | Major Depressive Disorder | 14 | 0%0/14 | 0%0/14 | 0%0/14 |
| Ketamine | Intensive 7-day Treatment for PTSD Combining Ketamine With Exposure Therapy NCT02727998Single Infusion of Ketamine With Prolonged Exposure | Phase 2 | Posttraumatic Stress Disorder | 14 | 0%0/14 | 0%0/14 | 0%0/14 |
| Ketamine | Intensive 7-day Treatment for PTSD Combining Ketamine With Exposure Therapy NCT02727998Midazolam With Prolonged Exposure | Phase 2 | Posttraumatic Stress Disorder | 14 | 0%0/14 | 0%0/14 | 0%0/14 |
| Ayahuasca | Antidepressant Effects of Ayahuasca: a Randomized Placebo Controlled Trial in Treatment Resistant Depression NCT02914769Ayahuasca | Phase 1/Phase 2 | Major Depression | 14 | 0%0/14 | 71%10/14 | not reported |
| Psilocybin | Efficacy of Psilocybin in OCD: a Double-Blind, Placebo-Controlled Study. NCT03356483Psilocybin | Phase 1 | Obsessive-Compulsive Disorder | 14 | 7%1/14 | 86%12/14 | 0%0/14 |
| Psilocybin | Efficacy of Psilocybin in OCD: a Double-Blind, Placebo-Controlled Study. NCT03356483Niacin | Phase 1 | Obsessive-Compulsive Disorder | 14 | 0%0/14 | 43%6/14 | 0%0/14 |
| Psilocybin | Efficacy of Psilocybin in OCD: a Double-Blind, Placebo-Controlled Study. NCT03356483Psilocybin-Unblinded | Phase 1 | Obsessive-Compulsive Disorder | 14 | 0%0/14 | 71%10/14 | 0%0/14 |
| Ketamine | Postpartum Perineal Pain After Obstetric Anal Sphincter Injuries NCT03470675Epidural Saline + IV Saline | Phase 4 | Pain, Postpartum Depression | 14 | 0%0/14 | 29%4/14 | 0%0/14 |
| Ketamine | Inpatient Single Dose Interventions for Alcohol Use Disorder NCT04562779XR Naltrexone | EARLY_Phase 1 | Alcohol Use Disorder, Severe | 14 | 0%0/14 | 36%5/14 | 0%0/14 |
| Ketamine | Research Study for Major Depressive Disorder: Investigation of Glutamate Medications NCT00419003Lamotrigine Pre-Treatment | Phase 4 | Major Depression | 13 | 0%0/13 | 38%5/13 | not reported |
| Ketamine | Research Study for Major Depressive Disorder: Investigation of Glutamate Medications NCT00419003Placebo Pre-Treatment | Phase 4 | Major Depression | 13 | 0%0/13 | 0%0/13 | not reported |
| Ketamine | Ketamine Versus Placebo for Treatment Resistant Major Depressive Disorder NCT01667926Ketamine | NA | Major Depressive Disorder | 13 | 15%2/13 | 23%3/13 | not reported |
| Ketamine | Ketamine Versus Placebo for Treatment Resistant Major Depressive Disorder NCT01667926Placebo | NA | Major Depressive Disorder | 13 | 0%0/13 | 8%1/13 | not reported |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610Active Dose 1 MDMA (125 mg) and Psychotherapy (Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 13 | 0%0/13 | 62%8/13 | 0%0/13 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610SRRs: Active Dose 1 | Phase 2 | Posttraumatic Stress Disorder | 13 | 0%0/13 | 0%0/13 | 0%0/13 |
| Ketamine | A Study to Investigate Evoked Potentials as Markers of Ketamine-induced Cortical Plasticity in Patients With Major Depressive Disorder NCT01957410Ketamine IV 0.5mg/kg | Phase 2 | Major Depressive Disorder | 13 | 0%0/13 | 77%10/13 | not reported |
| Ketamine | Ketamine in Adolescents With Treatment-Resistant Depression NCT02078817Ketamine | Phase 2 | Major Depressive Disorder | 13 | 0%0/13 | 38%5/13 | 0%0/13 |
| MDMA | MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness NCT02427568MDMA-assisted Therapy (125 mg) (Blinded) | Phase 2 | Anxiety | 13 | 0%0/13 | 85%11/13 | 0%0/13 |
| MDMA | MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness NCT02427568MDMA Group Open-label MDMA-assisted Therapy (125 mg) | Phase 2 | Anxiety | 13 | 0%0/13 | 23%3/13 | 0%0/13 |
| MDMA | MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness NCT02427568MDMA-assisted Therapy Group 12-month Follow-up | Phase 2 | Anxiety | 13 | 23%3/13 | 23%3/13 | 8%1/13 |
| Ketamine | Ketamine for Treatment Resistant Late-Life Depression NCT02556606Midazolam 0.03 mg/kg | Phase 3 | Treatment Resistant Depressive Disorder | 13 | 8%1/13 | 100%13/13 | 0%0/13 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318Post-Treatment (PT) Phase: Esketamine 28 mg | Phase 2 | Depression | 13 | 0%0/13 | 46%6/13 | 0%0/13 |
| Psilocybin | Persisting Effects of Psilocybin NCT02971605Psilocybin | Phase 1/Phase 2 | Healthy | 13 | 0%0/13 | 23%3/13 | 0%0/13 |
| Ketamine | Ketamine as an Adjunctive Therapy for Major Depression NCT03256162Ketamine | Phase 1 | Major Depressive Episode, Unipolar Depression | 13 | 0%0/13 | 0%0/13 | 0%0/13 |
| Ketamine | Inpatient Single Dose Interventions for Alcohol Use Disorder NCT04562779IV Ketamine | EARLY_Phase 1 | Alcohol Use Disorder, Severe | 13 | 0%0/13 | 46%6/13 | 0%0/13 |
| MDMA | Study Comparing Two Versus Three Active MDMA-assisted Sessions in U.S. Military Veterans With Chronic PTSD NCT04784143Two Sessions of MDMA-assisted Therapy | Phase 2 | PTSD | 13 | 0%0/13 | 100%13/13 | 0%0/13 |
| Ketamine | Adding Trauma-focused Psychotherapy to Ketamine Treatment for Chronic PTSD NCT04889664Ketamine and Written Exposure Therapy | Phase 2 | PTSD | 13 | 0%0/13 | 100%13/13 | 0%0/13 |
| Ketamine | KET-RO Plus RO DBT for Treatment Resistant Depression NCT06138691Ketamine + RO DBT | Phase 1 | Treatment Resistant Depression | 13 | 0%0/13 | 0%0/13 | 0%0/13 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Blinded Full Dose MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 12 | 0%0/12 | 67%8/12 | 0%0/12 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Open-Label Full Dose MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 12 | 0%0/12 | 33%4/12 | 0%0/12 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405SRRs: Full Dose | Phase 2 | Posttraumatic Stress Disorder | 12 | 0%0/12 | 100%12/12 | 0%0/12 |
| Ketamine | Ketamine For Suicidal Ideation NCT01507181Ketamine | Phase 4 | Suicidal Ideation | 12 | 42%5/12 | 100%12/12 | not reported |
| Ketamine | Ketamine For Suicidal Ideation NCT01507181Midazolam | Phase 4 | Suicidal Ideation | 12 | 0%0/12 | 100%12/12 | not reported |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610Open-Label Session: Active Dose 1 | Phase 2 | Posttraumatic Stress Disorder | 12 | 0%0/12 | 42%5/12 | 0%0/12 |
| Ketamine | The Effects of Ketamine on Respiratory Stimulation and Transpulmonary Pressures NCT01969227Ketamine Infusion (5 Then 10 mcg/kg/Min) During Propofol Sedation | NA | Mechanical Ventilation, Airway Patency | 12 | 0%0/12 | 0%0/12 | 0%0/12 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo to Esketamine 56mg (Panel A and B: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 12 | 0%0/12 | 92%11/12 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 28 mg: Follow up Phase | Phase 2 | Treatment Resistant Depressive Disorder | 12 | 8%1/12 | 33%4/12 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 84 mg (Panel A: Period 1) | Phase 2 | Treatment Resistant Depressive Disorder | 12 | 0%0/12 | 83%10/12 | not reported |
| Ketamine | Ketamine for Depression and Suicide Risk NCT02094898Ketamine Infusion | Phase 2 | Depression, Suicide | 12 | 17%2/12 | 100%12/12 | 8%1/12 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Intranasal Esketamine Plus an Oral Antidepressant in Elderly Participants With Treatment-resistant Depression NCT02422186Follow-up Phase: Intranasal Esketamine + Oral AD (2 Weeks) | Phase 3 | Depressive Disorder, Treatment-Resistant | 12 | 0%0/12 | 8%1/12 | 0%0/12 |
| Ketamine | Sequential Therapy for the Treatment of Severe Bipolar Depression. NCT02974010Ketamine Followed by NRX-101 | Phase 2 | Bipolar Depression, Suicidal Ideas | 12 | 0%0/12 | 67%8/12 | 0%0/12 |
| Ketamine | Ketamine as an Adjunctive Therapy for Major Depression NCT03256162Midazolam | Phase 1 | Major Depressive Episode, Unipolar Depression | 12 | 0%0/12 | 0%0/12 | 0%0/12 |
| Psilocybin | Safety and Efficacy of Psilocybin for Body Dysmorphic Disorder NCT04656301Psilocybin | Phase 2 | Body Dysmorphic Disorders | 12 | 0%0/12 | 92%11/12 | 0%0/12 |
| Psilocybin | Psilocybin Therapy for Depression and Anxiety in Parkinson's Disease NCT04932434Psilocybin Therapy | Phase 2 | Parkinson Disease, Depression | 12 | 0%0/12 | 92%11/12 | 0%0/12 |
| Psilocybin | Frontline Clinician Psilocybin Study NCT05163496Open-label Psilocybin (for Placebo Participants) | Phase 3 | Burnout, Caregiver, Burnout, Professional | 12 | 0%0/12 | 0%0/12 | 0%0/12 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Full Dose Group 12 Month Follow-Up | Phase 2 | Posttraumatic Stress Disorder | 11 | 0%0/11 | 0%0/11 | 0%0/11 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT0179361012 Month Follow-up: Active Dose 1 | Phase 2 | Posttraumatic Stress Disorder | 11 | 0%0/11 | 18%2/11 | 0%0/11 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 28 mg (Panel A: Period 1) | Phase 2 | Treatment Resistant Depressive Disorder | 11 | 0%0/11 | 73%8/11 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 14 mg (Panel B: Period 1) | Phase 2 | Treatment Resistant Depressive Disorder | 11 | 0%0/11 | 55%6/11 | not reported |
| Ketamine | Ketamine as a Rapidly-Acting Antidepressant in Depressed Emergency Department Patients NCT02106325Ketamine | Phase 2 | Depression | 11 | 9%1/11 | 73%8/11 | 0%0/11 |
| Ketamine | Ketamine for Treatment Resistant Late-Life Depression NCT02556606Ketamine 0.50 mg/kg | Phase 3 | Treatment Resistant Depressive Disorder | 11 | 0%0/11 | 100%11/11 | 0%0/11 |
| Ketamine | A Study to Evaluate the Efficacy, Safety and Tolerability of Fixed Doses of Intranasal Esketamine in Japanese Participants With Treatment Resistant Depression NCT02918318PT Phase: Esketamine 56 mg | Phase 2 | Depression | 11 | 0%0/11 | 36%4/11 | 0%0/11 |
| Ketamine | Trial of the Rapid Antisuicidal Effects of Intranasal Ketamine in Comorbid Depression and Alcohol Abuse NCT03539887Placebo | Phase 3 | Suicidal Ideation, Depression | 11 | 0%0/11 | 36%4/11 | 0%0/11 |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129MIJ821 0.16 mg/kg Weekly* | Phase 2 | Depressive Disorder, Treatment-Resistant | 11 | 0%0/11 | 64%7/11 | 0%0/11 |
| Ketamine | EEG Characteristics in ECT NCT04022226Methohexital | EARLY_Phase 1 | Electroconvulsive Therapy, Direct Current Electroencephalogram | 11 | 0%0/11 | 0%0/11 | 0%0/11 |
| Ketamine | Ketamine for the Treatment of Opioid Use Disorder and Depression NCT04177706Group A (Ketamine) | Phase 2 | Depression, Opioid-use Disorder | 11 | 0%0/11 | 0%0/11 | 0%0/11 |
| Ketamine | Treatment Resistant Depression (Pilot) NCT01179009Ketamine 100-hour Infusion | NA | Depressive Disorder, Treatment-Resistant | 10 | 0%0/10 | 100%10/10 | 0%0/10 |
| Ketamine | Treatment Resistant Depression (Pilot) NCT01179009Ketamine 40-minute Infusion | NA | Depressive Disorder, Treatment-Resistant | 10 | 0%0/10 | 100%10/10 | 0%0/10 |
| Psilocybin | Effects and Therapeutic Potential of Psilocybin in Alcohol Dependence NCT01534494Psilocybin | Phase 2 | Alcohol Dependence | 10 | 0%0/10 | 70%7/10 | 0%0/10 |
| Ketamine | Ketamine as a Rapidly-Acting Antidepressant in Depressed Emergency Department Patients NCT02106325Diphenhydramine | Phase 2 | Depression | 10 | 0%0/10 | 80%8/10 | 0%0/10 |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129MIJ821 0.16 mg/kg Every Other Week | Phase 2 | Depressive Disorder, Treatment-Resistant | 10 | 10%1/10 | 60%6/10 | 0%0/10 |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129MIJ821 0.32 mg/kg Weekly | Phase 2 | Depressive Disorder, Treatment-Resistant | 10 | 0%0/10 | 70%7/10 | 0%0/10 |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129Ketamine 0.5 mg/kg Weekly | Phase 2 | Depressive Disorder, Treatment-Resistant | 10 | 0%0/10 | 60%6/10 | 0%0/10 |
| Ketamine | Ketamine and Prolonged Exposure in PTSD NCT03960658Ketamine and Prolonged Exposure | Phase 1/Phase 2 | Post-traumatic Stress Disorder | 10 | 0%0/10 | 30%3/10 | 0%0/10 |
| Ketamine | Ketamine for the Treatment of Opioid Use Disorder and Depression NCT04177706Group B (Placebo) | Phase 2 | Depression, Opioid-use Disorder | 10 | 0%0/10 | 0%0/10 | 0%0/10 |
| Ketamine | Ketamine Infusion for Comorbid PTSD and Chronic Pain NCT04322968Chronic Pain With PTSD+IV Ketamine Infusion | Phase 3 | PTSD, Chronic Pain | 10 | 0%0/10 | 0%0/10 | 0%0/10 |
| Ketamine | Ketamine Infusion for Comorbid PTSD and Chronic Pain NCT04322968Chronic Pain Without PTSD+IV Ketamine Infusion | Phase 3 | PTSD, Chronic Pain | 10 | 0%0/10 | 0%0/10 | 0%0/10 |
| Ketamine | Ketamine Infusion for Comorbid PTSD and Chronic Pain NCT04322968Chronic Pain Without PTSD+IV Ketorolac Infusion | Phase 3 | PTSD, Chronic Pain | 10 | 0%0/10 | 0%0/10 | 0%0/10 |
| MDMA | Study Comparing Two Versus Three Active MDMA-assisted Sessions in U.S. Military Veterans With Chronic PTSD NCT04784143Three Sessions of MDMA-assisted Therapy | Phase 2 | PTSD | 10 | 0%0/10 | 100%10/10 | 0%0/10 |
| MDMA | Study of 3,4-Methylenedioxymethamphetamine-assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00353938Full Dose MDMA-assisted Therapy (125 mg Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 9 | 22%2/9 | 89%8/9 | 0%0/9 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610Active Dose 2 MDMA (100 mg) and Psychotherapy (Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 9 | 11%1/9 | 67%6/9 | 0%0/9 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610Open-Label Session: Active Dose 2 | Phase 2 | Posttraumatic Stress Disorder | 9 | 11%1/9 | 33%3/9 | 0%0/9 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT0179361012 Month Follow-up: Active Dose 2 | Phase 2 | Posttraumatic Stress Disorder | 9 | 11%1/9 | 11%1/9 | 0%0/9 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610SRRs: Active Dose 2 | Phase 2 | Posttraumatic Stress Disorder | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| Ketamine | Ketamine for Suicidality in Bipolar Depression NCT01944293Midazolam | Phase 1/Phase 2 | Bipolar Disorder, Major Depressive Episode | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| Ketamine | Ketamine and Nitroprusside for Depression NCT03102736Nitroprusside and Ketamine | Phase 2 | Depression | 9 | 0%0/9 | 44%4/9 | 0%0/9 |
| Ketamine | Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression NCT03756129MIJ821 0.32 mg/kg Every Other Week | Phase 2 | Depressive Disorder, Treatment-Resistant | 9 | 33%3/9 | 67%6/9 | 0%0/9 |
| MDMA | Effect of Stimulant Drugs on Social Perception NCT03790618Placebo | Phase 1 | Healthy, MDMA ('Ecstasy') | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| MDMA | Effect of Stimulant Drugs on Social Perception NCT03790618Low Dose MDMA | Phase 1 | Healthy, MDMA ('Ecstasy') | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| MDMA | Effect of Stimulant Drugs on Social Perception NCT03790618High Dose MDMA | Phase 1 | Healthy, MDMA ('Ecstasy') | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| MDMA | Effect of Stimulant Drugs on Social Perception NCT03790618Methamphetamine | Phase 1 | Healthy, MDMA ('Ecstasy') | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| Ketamine | Ketamine Treatment Effects on Synaptic Plasticity in Depression NCT04091971Depressed Adults With Current MDD | Phase 4 | Major Depressive Disorder | 9 | 0%0/9 | 56%5/9 | 0%0/9 |
| Ketamine | Ketamine Infusion for Comorbid PTSD and Chronic Pain NCT04322968Chronic Pain With PTSD+IV Ketorolac Infusion | Phase 3 | PTSD, Chronic Pain | 9 | 0%0/9 | 0%0/9 | 0%0/9 |
| Psilocybin | Visual Surround Suppression and Perceptual Expectation Under Psilocybin NCT04424225Psilocybin | Phase 1 | Perception Disturbance, Visual Suppression | 9 | 0%0/9 | 67%6/9 | 0%0/9 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005MAD Cohort 2 | Phase 1 | Major Depressive Disorder | 9 | 0%0/9 | 22%2/9 | 0%0/9 |
| Psilocybin | Psilocybin in Co-occuring Major Depressive Disorder and Borderline Personality Disorder NCT05399498Experimental: Psilocybin | Phase 2 | Borderline Personality Disorder, Major Depressive Disorder | 9 | 11%1/9 | 78%7/9 | 0%0/9 |
| MDMA | MDMA-Assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00090064Placebo With Therapy | Phase 2 | Posttraumatic Stress Disorder | 8 | 0%0/8 | 100%8/8 | 0%0/8 |
| MDMA | MDMA-Assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00090064SRRs: Placebo With Therapy | Phase 2 | Posttraumatic Stress Disorder | 8 | 0%0/8 | 100%8/8 | 0%0/8 |
| Ketamine | Research Study for Major Depressive Disorder: Investigation of Glutamate Medications NCT00419003Placebo | Phase 4 | Major Depression | 8 | 0%0/8 | 63%5/8 | not reported |
| LSD | Lysergic Acid Diethylamide (LSD)-Assisted Psychotherapy in People With Illness-related Anxiety NCT00920387Full Dose LSD (200 mcg Stage 1) | Phase 2 | Anxiety | 8 | 13%1/8 | 100%8/8 | 13%1/8 |
| Ketamine | N-methyl-D-aspartate Antagonist (Ketamine) Augmentation of Electroconvulsive Treatment for Severe Major Depression NCT01260649Placebo | Phase 4 | Major Depressive Disorder | 8 | 13%1/8 | 38%3/8 | 0%0/8 |
| Ketamine | NMDA Antagonists in Bipolar Depression NCT01833897Ketamine and DCS Treatment | Phase 4 | Bipolar Disorder | 8 | 0%0/8 | 50%4/8 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo to Esketamine 28mg (Panel A: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 8 | 0%0/8 | 50%4/8 | not reported |
| Ketamine | Physiological and Cognitive Biomarkers for Ketamine's Antidepressant Effects NCT02669043Ketamine | NA | Depression | 8 | 0%0/8 | 0%0/8 | 0%0/8 |
| Ketamine | Ketamine to Improve Recovery After Cesarean Delivery - Part 1 NCT04037085Ketamine | Phase 2 | Obstetric Pain, Postpartum Depression | 8 | 0%0/8 | 88%7/8 | 0%0/8 |
| Ketamine | Ketamine to Prevent PPD After Cesarean NCT04227704Ketamine SC | Phase 3 | Postpartum Depression | 8 | 0%0/8 | 75%6/8 | 0%0/8 |
| Ketamine | Ketamine to Prevent PPD After Cesarean NCT04227704Ketamine IVI | Phase 3 | Postpartum Depression | 8 | 0%0/8 | 75%6/8 | 0%0/8 |
| Psilocybin | Visual Surround Suppression and Perceptual Expectation Under Psilocybin NCT04424225Niacin | Phase 1 | Perception Disturbance, Visual Suppression | 8 | 0%0/8 | 63%5/8 | 0%0/8 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Blinded Low Dose MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 7 | 14%1/7 | 86%6/7 | 0%0/7 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Blinded Medium Dose MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 7 | 0%0/7 | 57%4/7 | 0%0/7 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Medium Dose Group 12 Month Follow-Up | Phase 2 | Posttraumatic Stress Disorder | 7 | 14%1/7 | 0%0/7 | 0%0/7 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405SRRS: Low Dose | Phase 2 | Posttraumatic Stress Disorder | 7 | 0%0/7 | 100%7/7 | 0%0/7 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405SRRs: Medium Dose | Phase 2 | Posttraumatic Stress Disorder | 7 | 0%0/7 | 100%7/7 | 0%0/7 |
| Ketamine | Treatment of Suicidal Ideation With Intravenous Ketamine Infusion NCT01887990Suicidal, Depression With Ketamine | NA | Depression, Suicidal Ideation | 7 | 0%0/7 | 14%1/7 | not reported |
| Ketamine | Treatment of Suicidal Ideation With Intravenous Ketamine Infusion NCT01887990Suicidal, Depression With Saline | NA | Depression, Suicidal Ideation | 7 | 0%0/7 | 0%0/7 | not reported |
| Ketamine | Ketamine for Suicidality in Bipolar Depression NCT01944293Ketamine | Phase 1/Phase 2 | Bipolar Disorder, Major Depressive Episode | 7 | 57%4/7 | 0%0/7 | 0%0/7 |
| Ketamine | Administration of Subanesthetic Dose of Ketamine and Electroconvulsive Treatment for Treatment Resistant Depression NCT02522377Ketamine Infusions | NA | Treatment Resistant Depression, Major Depressive Disorder | 7 | 0%0/7 | 14%1/7 | 0%0/7 |
| Ketamine | Ketamine and Nitroprusside for Depression NCT03102736Placebo and Ketamine | Phase 2 | Depression | 7 | 0%0/7 | 100%7/7 | 0%0/7 |
| Ketamine | Ketamine to Prevent PPD After Cesarean NCT04227704Control | Phase 3 | Postpartum Depression | 7 | 0%0/7 | 100%7/7 | 0%0/7 |
| Ketamine | Research Study for Major Depressive Disorder: Investigation of Glutamate Medications NCT00419003Riluzole Group | Phase 4 | Major Depression | 6 | 0%0/6 | 100%6/6 | not reported |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Open-Label Low Dose MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 6 | 17%1/6 | 100%6/6 | 0%0/6 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Open-Label Medium Dose MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 67%4/6 | 0%0/6 |
| MDMA | Study Comparing Three Doses of MDMA Along With Therapy in Veterans With Posttraumatic Stress Disorder NCT01211405Low Dose Group 12 Month Follow-Up | Phase 2 | Posttraumatic Stress Disorder | 6 | 17%1/6 | 0%0/6 | 0%0/6 |
| Ketamine | N-methyl-D-aspartate Antagonist (Ketamine) Augmentation of Electroconvulsive Treatment for Severe Major Depression NCT01260649Ketamine | Phase 4 | Major Depressive Disorder | 6 | 0%0/6 | 33%2/6 | 0%0/6 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610Comparator-dose MDMA (40 mg) and Psychotherapy (Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 17%1/6 | 0%0/6 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610SRRs: Comparator | Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 83%5/6 | 0%0/6 |
| Ketamine | Effects of Low Dose Ketamine Given at Induction of Anesthesia on Postoperative Mood in Patients With Depressive Symptoms NCT02422303Ketamine Group | NA | Depression, Major Depressive Disorder | 6 | 0%0/6 | 0%0/6 | not reported |
| Ketamine | Effects of Low Dose Ketamine Given at Induction of Anesthesia on Postoperative Mood in Patients With Depressive Symptoms NCT02422303No Ketamine Group | NA | Depression, Major Depressive Disorder | 6 | 0%0/6 | 0%0/6 | not reported |
| MDMA | MDMA-Assisted Cognitive-Behavioral Conjoint Therapy (CBCT) in Dyads in Which 1 Member Has Chronic PTSD NCT02876172PTSD Patients Open-label CBCT and MDMA-assisted Therapy (up to 2 Months Post Last Experimental Dose) | Phase 1/Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 100%6/6 | 0%0/6 |
| MDMA | MDMA-Assisted Cognitive-Behavioral Conjoint Therapy (CBCT) in Dyads in Which 1 Member Has Chronic PTSD NCT02876172CSO Patients Open-label CBCT and MDMA-assisted Therapy (up to 2 Months Post Last Experimental Dose) | Phase 1/Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 100%6/6 | 0%0/6 |
| MDMA | MDMA-Assisted Cognitive-Behavioral Conjoint Therapy (CBCT) in Dyads in Which 1 Member Has Chronic PTSD NCT02876172PTSD Patients at 6-month Follow-up | Phase 1/Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 33%2/6 | 0%0/6 |
| MDMA | MDMA-Assisted Cognitive-Behavioral Conjoint Therapy (CBCT) in Dyads in Which 1 Member Has Chronic PTSD NCT02876172CSO Patients at 6-month Follow-up | Phase 1/Phase 2 | Posttraumatic Stress Disorder | 6 | 0%0/6 | 33%2/6 | 0%0/6 |
| Ketamine | The UTHealth Ketamine Project NCT02882711Ketamine | Phase 2 | Treatment Resistant Depression, Major Depressive Disorder | 6 | 17%1/6 | 17%1/6 | 0%0/6 |
| Ketamine | Reducing Adolescent Suicide Risk: Safety, Efficacy, and Connectome Phenotypes of Intravenous Ketamine NCT04613453Midazolam Infusion-Blinded | Phase 2 | Adolescent Suicide, Adolescent Depression | 6 | 50%3/6 | 83%5/6 | 0%0/6 |
| Ketamine | Reducing Adolescent Suicide Risk: Safety, Efficacy, and Connectome Phenotypes of Intravenous Ketamine NCT04613453Ketamine Infusion-Unblinded | Phase 2 | Adolescent Suicide, Adolescent Depression | 6 | 0%0/6 | 100%6/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005SAD Cohort 1 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 17%1/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005SAD Cohort 2 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 0%0/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005SAD Cohort 3 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 17%1/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005SAD Cohort 4 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 17%1/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005SAD Cohort 5 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 17%1/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005SAD Cohort 6 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 33%2/6 | 0%0/6 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005MAD Cohort 1 | Phase 1 | Major Depressive Disorder | 6 | 0%0/6 | 17%1/6 | 0%0/6 |
| MDMA | Study of 3,4-Methylenedioxymethamphetamine-assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00353938Active Placebo MDMA-assisted Therapy (25 mg Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 5 | 0%0/5 | 60%3/5 | 0%0/5 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT01689740Blinded Full Dose MDMA-assisted Therapy (125 mg) (Stage 1) | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 5 | 0%0/5 | 80%4/5 | 0%0/5 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT0168974012 Month Follow-Up: Blinded Full Dose | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 5 | 0%0/5 | 20%1/5 | 0%0/5 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT01689740SRRs: Full Dose | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 5 | 0%0/5 | 100%5/5 | 0%0/5 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT01793610Crossover Open-Label Sessions: Comparator Dose | Phase 2 | Posttraumatic Stress Disorder | 5 | 0%0/5 | 60%3/5 | 0%0/5 |
| MDMA | Dose-Response Study of MDMA-assisted Psychotherapy in People With PTSD NCT0179361012 Month Follow-up: Comparator Dose | Phase 2 | Posttraumatic Stress Disorder | 5 | 0%0/5 | 20%1/5 | 0%0/5 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo to Esketamine 14mg (Panel B: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 5 | 0%0/5 | 100%5/5 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo to Esketamine 84 mg (Panel A: Period 2) | Phase 2 | Treatment Resistant Depressive Disorder | 5 | 0%0/5 | 100%5/5 | not reported |
| MDMA | MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness NCT02427568Placebo With Therapy (Blinded) | Phase 2 | Anxiety | 5 | 0%0/5 | 40%2/5 | 0%0/5 |
| MDMA | MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness NCT02427568Placebo Group Open-label Crossover to Unblinded MDMA-assisted Therapy (125 mg) | Phase 2 | Anxiety | 5 | 0%0/5 | 80%4/5 | 0%0/5 |
| MDMA | MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness NCT02427568Placebo With Therapy Group 12-month Follow-up | Phase 2 | Anxiety | 5 | 0%0/5 | 40%2/5 | 0%0/5 |
| Ketamine | Administration of Subanesthetic Dose of Ketamine and Electroconvulsive Treatment for Treatment Resistant Depression NCT02522377Midazolam | NA | Treatment Resistant Depression, Major Depressive Disorder | 5 | 0%0/5 | 0%0/5 | 0%0/5 |
| Ketamine | Ketamine for Treatment Resistant Late-Life Depression NCT02556606Ketamine 0.25 mg/kg | Phase 3 | Treatment Resistant Depressive Disorder | 5 | 0%0/5 | 100%5/5 | 0%0/5 |
| Ketamine | Ketamine for Relapse Prevention in Recurrent Depressive Disorder NCT02661061Ketamine | Phase 1 | Depression, Relapse | 5 | 0%0/5 | 20%1/5 | 0%0/5 |
| Ketamine | Low Dose Intravenous Ketamine in Treatment Resistant Depression Patients NCT02935595Ketamine | Phase 2 | Treatment Resistant Depression | 5 | 0%0/5 | 20%1/5 | 0%0/5 |
| Ketamine | Sequential Therapy for the Treatment of Severe Bipolar Depression. NCT02974010Ketamine Followed by Lurasidone | Phase 2 | Bipolar Depression, Suicidal Ideas | 5 | 0%0/5 | 60%3/5 | 0%0/5 |
| Ketamine | Intraoperative Ketamine Versus Saline in Depressed Patients Undergoing Anesthesia for Non-cardiac Surgery NCT03861988Open Label Ketamine | Phase 4 | Major Depressive Disorder, Surgery | 5 | 0%0/5 | 20%1/5 | 0%0/5 |
| Ketamine | Reducing Adolescent Suicide Risk: Safety, Efficacy, and Connectome Phenotypes of Intravenous Ketamine NCT04613453Ketamine Infusion-Blinded | Phase 2 | Adolescent Suicide, Adolescent Depression | 5 | 40%2/5 | 100%5/5 | 0%0/5 |
| Psilocybin | Open-label Study to Assess the Safety and Efficacy of Psilocybin With Psychotherapy in Adult Participants With Fibromyalgia NCT05128162Open Label Dosing Arm (15mg and 25mg) | Phase 2 | Fibromyalgia | 5 | 0%0/5 | 80%4/5 | 0%0/5 |
| Ketamine | KAP for Depression in Abstinent Opioid Users NCT05193318Ketamine-assisted Psychotherapy | Phase 2 | Opioid Use Disorder, Severe, in Sustained Remission, Opioid Use Disorder, Severe, in Early Remission | 5 | 0%0/5 | 60%3/5 | 0%0/5 |
| MDMA | Study of 3,4-Methylenedioxymethamphetamine-assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00353938Full Dose MDMA-assisted Therapy (125 mg Stage 2) | Phase 2 | Posttraumatic Stress Disorder | 4 | 0%0/4 | 50%2/4 | 0%0/4 |
| LSD | Lysergic Acid Diethylamide (LSD)-Assisted Psychotherapy in People With Illness-related Anxiety NCT00920387Active Placebo LSD (20 mcg Stage 1) | Phase 2 | Anxiety | 4 | 25%1/4 | 100%4/4 | 0%0/4 |
| MDMA | Randomized, Double-blind, Controlled of MDMA-assisted Psychotherapy in 12 Subjects With PTSD NCT01958593MDMA-assisted Therapy (Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| MDMA | Randomized, Double-blind, Controlled of MDMA-assisted Psychotherapy in 12 Subjects With PTSD NCT01958593SRRs: MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Esketamine 14 mg: Follow up Phase | Phase 2 | Treatment Resistant Depressive Disorder | 4 | 0%0/4 | 25%1/4 | not reported |
| MDMA | Phase 2 Pilot Safety Study of MDMA-assisted Therapy for Social Anxiety in Autistic Adults NCT02008396Group 1: MDMA-assisted Therapy 75mg/100mg | Phase 2 | Social Anxiety in Autistic Adults | 4 | 0%0/4 | 25%1/4 | 0%0/4 |
| MDMA | Phase 2 Pilot Safety Study of MDMA-assisted Therapy for Social Anxiety in Autistic Adults NCT02008396Group 2: MDMA-assisted Therapy 100mg/125mg | Phase 2 | Social Anxiety in Autistic Adults | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| MDMA | Phase 2 Pilot Safety Study of MDMA-assisted Therapy for Social Anxiety in Autistic Adults NCT02008396Inactive Placebo With Psychotherapy (Stage 1) | Phase 2 | Social Anxiety in Autistic Adults | 4 | 0%0/4 | 25%1/4 | 0%0/4 |
| Ketamine | Ketamine for Treatment Resistant Late-Life Depression NCT02556606Ketamine 0.10 mg/kg | Phase 3 | Treatment Resistant Depressive Disorder | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| Ketamine | Ketamine for Relapse Prevention in Recurrent Depressive Disorder NCT02661061Midazolam | Phase 1 | Depression, Relapse | 4 | 0%0/4 | 25%1/4 | 0%0/4 |
| Ketamine | Sequential Therapy for the Treatment of Severe Bipolar Depression. NCT02974010Saline Followed by NRX-101 | Phase 2 | Bipolar Depression, Suicidal Ideas | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| MDMA | Study of Safety and Effects of MDMA-assisted Psychotherapy for Treatment of PTSD (Canada) NCT03485287MDMA-assisted Therapy (100 to 125 mg) | Phase 2 | Posttraumatic Stress Disorder | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| Ketamine | The Pharmacokinetics of Ketamine in the Breast Milk of Lactating Women NCT04285684Ketamine During Lactation | EARLY_Phase 1 | Ketamine, Lactation | 4 | 0%0/4 | 0%0/4 | 0%0/4 |
| Ketamine | Phase 1 Evaluation of (2R,6R)-Hydroxynorketamine NCT04711005CSF Capture Cohort 1 | Phase 1 | Major Depressive Disorder | 4 | 0%0/4 | 100%4/4 | 0%0/4 |
| MDMA | Study of 3,4-Methylenedioxymethamphetamine-assisted Psychotherapy in People With Posttraumatic Stress Disorder NCT00353938Full or Larger Dose MDMA-assisted Therapy (125 or 150 mg Stage 3) | Phase 2 | Posttraumatic Stress Disorder | 3 | 0%0/3 | 33%1/3 | 0%0/3 |
| MDMA | Randomized Placebo-controlled Study of MDMA-assisted Therapy in People With PTSD - Israel NCT00402298Full Dose (125 mg) MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 3 | 0%0/3 | 67%2/3 | 0%0/3 |
| LSD | Lysergic Acid Diethylamide (LSD)-Assisted Psychotherapy in People With Illness-related Anxiety NCT00920387Full Dose LSD (200 mcg Stage 2) | Phase 2 | Anxiety | 3 | 0%0/3 | 100%3/3 | 0%0/3 |
| MDMA | Additional MDMA-assisted Therapy for People Who Relapsed After MDMA-assisted Therapy Trial NCT014583273,4-methylenedoxymethamphetamine (MDMA)-Assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 3 | 33%1/3 | 33%1/3 | 0%0/3 |
| Ketamine | Oral Ketamine in the Treatment of Depression and Anxiety in Patients With Cancer NCT01680172Ketamine | Phase 2 | Cancer, Depression | 3 | 0%0/3 | 100%3/3 | not reported |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT01689740Blinded Active Placebo MDMA-assisted Therapy (Stage 1) | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 3 | 0%0/3 | 33%1/3 | 0%0/3 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT01689740SRRs: Active Placebo | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 3 | 0%0/3 | 100%3/3 | 0%0/3 |
| Ketamine | Ketamine for Depression Relapse Prevention Following ECT NCT02414932Ketamine | EARLY_Phase 1 | Depression | 3 | 0%0/3 | 67%2/3 | 0%0/3 |
| Ketamine | Ketamine for Depression Relapse Prevention Following ECT NCT02414932Midazolam | EARLY_Phase 1 | Depression | 3 | 0%0/3 | 0%0/3 | 0%0/3 |
| Ketamine | A Study to Evaluate the Efficacy, Safety, and Tolerability of Intranasal Esketamine Plus an Oral Antidepressant in Elderly Participants With Treatment-resistant Depression NCT02422186Follow-up Phase: Oral AD + Intranasal Placebo (2 Weeks) | Phase 3 | Depressive Disorder, Treatment-Resistant | 3 | 0%0/3 | 33%1/3 | 0%0/3 |
| Ketamine | The Effect of Ketamine on the Length of Hospital Stay of Patients Hospitalized With Suicidal Ideation. NCT02997722Ketamine Infusion | Phase 4 | Suicidal Ideation | 3 | 0%0/3 | 33%1/3 | 0%0/3 |
| Ketamine | Ketamine Tolerated Dose for Postpartum Depression and Pain After Cesarean Delivery (PREPARE 1) NCT05907213Ketamine (Ketalar) Dose Level 1 | Phase 1 | Pain, Postoperative, Depression, Postpartum | 3 | 0%0/3 | 100%3/3 | 0%0/3 |
| Ketamine | Ketamine Tolerated Dose for Postpartum Depression and Pain After Cesarean Delivery (PREPARE 1) NCT05907213Ketamine (Ketalar) Dose Level 2 | Phase 1 | Pain, Postoperative, Depression, Postpartum | 3 | 0%0/3 | 100%3/3 | 0%0/3 |
| Ketamine | Ketamine Tolerated Dose for Postpartum Depression and Pain After Cesarean Delivery (PREPARE 1) NCT05907213Ketamine (Ketalar) Dose Level 3 | Phase 1 | Pain, Postoperative, Depression, Postpartum | 3 | 0%0/3 | 100%3/3 | 0%0/3 |
| Ketamine | Ketamine Tolerated Dose for Postpartum Depression and Pain After Cesarean Delivery (PREPARE 1) NCT05907213Ketamine (Ketalar) Dose Level 4 | Phase 1 | Pain, Postoperative, Depression, Postpartum | 3 | 0%0/3 | 100%3/3 | 0%0/3 |
| MDMA | MDMA-assisted Therapy in People With Anxiety Related to Advanced Stage Cancer NCT00252174Stage 1, Control | Phase 2 | Anxiety Disorder, Cancer | 2 | 0%0/2 | 0%0/2 | 0%0/2 |
| MDMA | Randomized Placebo-controlled Study of MDMA-assisted Therapy in People With PTSD - Israel NCT00402298Low Dose (25 mg) MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| Ketamine | Use of Ketamine to Enhance Electroconvulsive Therapy (ECT) in Depression NCT01309581Ketamine | NA | Major Depression, Bipolar Depression | 2 | 0%0/2 | 100%2/2 | not reported |
| Ketamine | Oral Ketamine in the Treatment of Depression and Anxiety in Patients With Cancer NCT01680172Placebo | Phase 2 | Cancer, Depression | 2 | 0%0/2 | 100%2/2 | not reported |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT01689740Lead In Open-Label: 125 mg MDMA-assisted Therapy | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT01689740Open-Label Full Dose MDMA-assisted Therapy (125 mg) (Stage 2) | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT0168974012 Month Follow-Up: Open-Label Full Dose Lead-In | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 2 | 0%0/2 | 0%0/2 | 0%0/2 |
| MDMA | Randomized, Double-blind, Placebo-Controlled Pilot Study of MDMA-assisted Therapy for PTSD NCT0168974012 Month Follow-Up: Active Placebo Dose | Phase 2 | Posttraumatic Stress Disorder (PTSD) | 2 | 0%0/2 | 0%0/3 | 0%0/2 |
| Ketamine | Treatment of Suicidal Ideation With Intravenous Ketamine Infusion NCT01887990Suicidal, Depression and Opioid Use With Ketamine | NA | Depression, Suicidal Ideation | 2 | 0%0/2 | 0%0/2 | not reported |
| Ketamine | Treatment of Suicidal Ideation With Intravenous Ketamine Infusion NCT01887990Suicidal, Depression and Opioid With Saline | NA | Depression, Suicidal Ideation | 2 | 0%0/2 | 0%0/2 | not reported |
| MDMA | Randomized, Double-blind, Controlled of MDMA-assisted Psychotherapy in 12 Subjects With PTSD NCT01958593Placebo With Therapy (Stage 1) | Phase 2 | Posttraumatic Stress Disorder | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| MDMA | Randomized, Double-blind, Controlled of MDMA-assisted Psychotherapy in 12 Subjects With PTSD NCT01958593Placebo With Therapy (Stage 2) | Phase 2 | Posttraumatic Stress Disorder | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| MDMA | Randomized, Double-blind, Controlled of MDMA-assisted Psychotherapy in 12 Subjects With PTSD NCT01958593SRRs: Placebo With Therapy | Phase 2 | Posttraumatic Stress Disorder | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| Ketamine | RCT: Fentanyl Plus Ketamine Versus Fentanyl Alone for Acute Burn Pain NCT03305055Fentanyl Plus Ketamine | Phase 4 | Acute Pain, Wound Care | 2 | 0%0/2 | 50%1/2 | 0%0/2 |
| Ketamine | RCT: Fentanyl Plus Ketamine Versus Fentanyl Alone for Acute Burn Pain NCT03305055Fentanyl Plus Saline | Phase 4 | Acute Pain, Wound Care | 2 | 0%0/2 | 50%1/2 | 0%0/2 |
| Ketamine | Ketamine for Severe Adolescent Depression: Intermediate-term Safety and Efficacy NCT03889756Midazolam | Phase 2/Phase 3 | Major Depressive Disorder | 2 | 0%0/2 | 100%2/2 | 0%0/2 |
| Ketamine | Ketamine-assisted Psychotherapy (KAP) for Patients With Existential Distress Associated With Non-operable GI Cancers NCT06001372Arm 1 | EARLY_Phase 1 | Gastrointestinal Cancer, Depression | 2 | 50%1/2 | 50%1/2 | 0%0/2 |
| Ketamine | Use of Ketamine to Enhance Electroconvulsive Therapy (ECT) in Depression NCT01309581Methohexitol | NA | Major Depression, Bipolar Depression | 1 | 0%0/1 | 100%1/1 | not reported |
| Ketamine | A Study to Evaluate the Safety and Efficacy of Intranasal Esketamine in Treatment-resistant Depression NCT01998958Placebo: Follow up Phase | Phase 2 | Treatment Resistant Depressive Disorder | 1 | 0%0/1 | 0%0/1 | not reported |
| Ketamine | Sequential Therapy for the Treatment of Severe Bipolar Depression. NCT02974010Saline Followed by Lurasidone | Phase 2 | Bipolar Depression, Suicidal Ideas | 1 | 0%0/1 | 100%1/1 | 0%0/1 |
| Ketamine | The Effect of Ketamine on the Length of Hospital Stay of Patients Hospitalized With Suicidal Ideation. NCT02997722Normal Saline Infusion | Phase 4 | Suicidal Ideation | 1 | 0%0/1 | 0%0/1 | 0%0/1 |
| Ketamine | Ketamine for Severe Adolescent Depression: Intermediate-term Safety and Efficacy NCT03889756Ketamine | Phase 2/Phase 3 | Major Depressive Disorder | 1 | 0%0/1 | 100%1/1 | 0%0/1 |
| Ketamine | Efficacy And Tolerability Of Sub-Anesthetic Ketamine In Postpartum Depression NCT04011592Ketamine 0.5 mg/kg | Phase 2 | Post Partum Depression | 1 | 0%0/1 | 100%1/1 | 0%0/1 |
| Ketamine | Efficacy And Tolerability Of Sub-Anesthetic Ketamine In Postpartum Depression NCT04011592Ketamine 0.2 mg/kg | Phase 2 | Post Partum Depression | 1 | 0%0/1 | 100%1/1 | 0%0/1 |
| Ketamine | Initiating Ketamine in Acutely Suicidal Patients in the Emergency Department NCT04260607Experimental-Ketamine | Phase 3 | Suicide, Suicide Threat | 1 | 0%0/1 | 100%1/1 | 0%0/1 |
| Ketamine | A Study of Esketamine Nasal Spray, Administered as Monotherapy, in Adult Participants With Treatment-resistant Depression NCT04599855OL Observation Period | Phase 4 | Depressive Disorder, Treatment-Resistant | 1 | 0%0/1 | 0%0/1 | 0%0/1 |
| MDMA | MDMA-assisted Therapy in People With Anxiety Related to Advanced Stage Cancer NCT00252174Stage 1, Active | Phase 2 | Anxiety Disorder, Cancer | 0 | not reported | not reported | not reported |
| MDMA | MDMA-assisted Therapy in People With Anxiety Related to Advanced Stage Cancer NCT00252174Stage 2, Active | Phase 2 | Anxiety Disorder, Cancer | 0 | not reported | not reported | not reported |
| Ketamine | Treatment Study of Bipolar Depression NCT00947791Ketamine/Midazolam | Phase 4 | Bipolar Disorder | 0 | not reported | not reported | not reported |
| Ketamine | Treatment Study of Bipolar Depression NCT00947791Midazolam/Ketamine | Phase 4 | Bipolar Disorder | 0 | not reported | not reported | not reported |
| MDMA | Effects of MDMA on Emotional and Social Memories NCT03050541Healthy Adult Volunteers-Placebo at Both Sessions | NA | Healthy | 0 | not reported | not reported | not reported |
| Ketamine | Initiating Ketamine in Acutely Suicidal Patients in the Emergency Department NCT04260607Placebo-Saline | Phase 3 | Suicide, Suicide Threat | 0 | not reported | not reported | not reported |