A Phase 2a Study to Evaluate the Safety and Tolerability of GM-2505 in Patients With MDD

Recruiting Phase 2 Interventional Study
Major Depressive Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
124 (estimated)
Sponsor
Gilgamesh Pharmaceuticals · Industry
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About This Trial
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 treatme…
Trial Locations
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Eligibility Criteria
Key Inclusion Criteria: 1. Patients are male or female, of any ethnic origin. 2. Patients are aged between 18 to 65 years, inclusive. 3. Patients meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnostic criteria for recurrent MDD without psychotic features, a…
Contacts

Jason Winters

6097385579

jason@gilgameshpharmaceutical.com

CONTACT