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RECRUITING
NCT06236880
PHASE2

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

Sponsor: Gilgamesh Pharmaceuticals

View on ClinicalTrials.gov

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

Interventions

DRUG

GM-2505

IV

Locations (1)

MAC Clinical Research

Manchester, United Kingdom