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A Phase 2a Study to Evaluate the Safety and Tolerability of GM-2505 in Patients With MDD
Sponsor: Gilgamesh Pharmaceuticals
Summary
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.
Official title: A Phase 2a Study to Evaluate the Safety and Tolerability of Two Repeated Doses of GM-2505 at a 2-Week Interval in Patients With Major Depressive Disorder.
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
124
Start Date
2024-01-31
Completion Date
2026-10
Last Updated
2026-02-09
Healthy Volunteers
No
Conditions
Interventions
GM-2505
IV
Locations (1)
MAC Clinical Research
Manchester, United Kingdom