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NCT Number: NCT06236880

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

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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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

MAC Clinical Research

Manchester, United Kingdom

Location status: Recruiting

Location contact

Babajida

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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:
  • (Part A) Patients need to be stable and must not have taken any SSRI or SNRI for at least 6 weeks prior to Screening and must be willing to avoid starting a new pharmacological treatment for MDD until the end of the study procedures and assessments. Discontinuing current treatment is not allowed if done for the purposes of achieving eligibility for this study.
  • (Part B) Patients need to be on stable treatment with any SSRI or SNRI for at least 6 weeks prior to screening and must be willing to remain on the SSRI or SNRI for the duration of the trial
  • Patients receiving any form of psychotherapy or counselling must have been receiving therapy at Screening and must be willing to remain in therapy until the end of the study procedures and assessments.

Key Exclusion Criteria:

  • Patient has current or past primary DSM-5 diagnosis of a psychotic disorder or MDD with psychotic features, bipolar, or related disorders. A current diagnosis of PTSD, complex PTSD and borderline personality disorder are exclusionary. Other psychiatric disorders besides MDD should not be the primary disorder.
  • In first degree relatives, a history of schizophrenia, psychosis, bipolar disorder, delusional disorder, paranoid personality disorder or schizoaffective disorder.
  • Current or prior (six weeks before Screening) use of any SSRI/SNRI medication (Part A only).
  • Current or prior (five weeks before Screening) use of any monoamine oxidase inhibitor ([MAO-I]; including phenelzine, tranylcypromine, isocarboxazid, iproniazid, selegiline, rasagiline, the reversible MAO-I moclobemide and the antibiotic linezolid).or any tricyclic antidepressant

Treatment and study plan

GM-2505

Drug

IV

Primary outcomes

  1. Safety and Tolerability (Part A, B, and C)

    Time frame: 99 Days

    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.

  2. MADRS Score (Part B and C)

    Time frame: 29 Days

    The estimated difference between Arm 1 and Arm 2 in the changes from baseline in MADRS-SIGMA total score

Secondary outcomes

  1. MADRS-SIGMA total score (Part A)

    Time frame: Days 14 and 29

    Change in MADRS-SIGMA total score between Baseline and Day 29 and comparison of Day 1 low dose vs moderate dose at Day 14

  2. MADRS-SIGMA total score (Part B and C)

    Time frame: All additional timepoints

    MADRS-SIGMA scores (change from baseline)

  3. MADRS-SIGMA total score (Part B and C)

    Time frame: Days 14, 29, 43, 71, and 99

    Response and Remission

  4. PK of GM-2505 (Part C)

    Time frame: Day 16

    Assess the pharmacokinetics of GM-2505 at very low, moderate, and high doses

Study contacts

Contact information is provided by the study sponsor or research team.

Jason Winters

CONTACT

[email protected]

6097385579

Sponsors and collaborators

Lead sponsor

Gilgamesh Pharmaceuticals

Industry

Registry information

Official study 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.

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Feb 1, 2024
Registry last updated
Feb 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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