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| ID | Type | Description | Link |
|---|---|---|---|
| 2023-000846-40 | EudraCT Number | ||
| M26-286 | Other Identifier | Gilgamesh Pharmaceuticals |
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This is a three-part Phase 2a study. The aim of Part A is to assess the safety and tolerability and preliminary antidepressant efficacy in patients with MDD who are not currently on an antidepressant therapy. The aim of Part B is to assess the antidepressant efficacy, safety and tolerability in patients with MDD who are partial responders while on a current and adequate single SSRI or SNRI treatment. Part C aims to replicate the monotherapy findings of Part A, but with a lower control group dose.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Low Dose to High Dose of GM-2505 | Experimental |
| |
| Moderate Dose to High Dose of GM-2505 | Experimental |
| |
| Experimental very low dose to very low dose of GM-2505 | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| GM-2505 | Drug | IV |
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety and Tolerability (Part A, B, and C) | The primary objective of this study is to evaluate the safety and tolerability of two doses of GM-2505 administered to MDD patients at a 2-week interval between doses. | 99 Days |
| MADRS Score (Part B and C) | The estimated difference between Arm 1 and Arm 2 in the changes from baseline in MADRS-SIGMA total score | 29 Days |
| Measure | Description | Time Frame |
|---|---|---|
| MADRS-SIGMA total score (Part A) | Change in MADRS-SIGMA total score between Baseline and Day 29 and comparison of Day 1 low dose vs moderate dose at Day 14 | Days 14 and 29 |
| MADRS-SIGMA total score (Part B and C) |
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Key Inclusion Criteria:
Patients are male or female, of any ethnic origin.
Patients are aged between 18 to 65 years, inclusive.
Patients meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnostic criteria for recurrent MDD without psychotic features, as assessed with the Mini-International Neuropsychiatric Interview (MINI) at Screening.
Current moderate to severe MDD diagnosis confirmed with a MADRS-SIGMA
Concomitant depression therapy:
Key Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jason Winters | Contact | 6097385579 | jason@gilgameshpharmaceutical.com |
| Name | Affiliation | Role |
|---|---|---|
| Gerard Marek, MD | Gilgamesh Pharmaceuticals | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| MAC Clinical Research | Recruiting | Manchester | United Kingdom |
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| ID | Term |
|---|---|
| D003865 | Depressive Disorder, Major |
| ID | Term |
|---|---|
| D003866 | Depressive Disorder |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
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MADRS-SIGMA scores (change from baseline)
| All additional timepoints |
| MADRS-SIGMA total score (Part B and C) | Response and Remission | Days 14, 29, 43, 71, and 99 |
| PK of GM-2505 (Part C) | Assess the pharmacokinetics of GM-2505 at very low, moderate, and high doses | Day 16 |