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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
126
IV
MAC Clinical Research
Manchester, United Kingdom
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.
Time frame: 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
Time frame: 29 Days
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
Time frame: Days 14 and 29
MADRS-SIGMA total score (Part B and C)
MADRS-SIGMA scores (change from baseline)
Time frame: All additional timepoints
MADRS-SIGMA total score (Part B and C)
Response and Remission
Time frame: 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
Time frame: Day 16
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