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A 14-week, multicentre, double-blind, randomised, placebo-controlled phase II study with an 8-week treatment period to assess the efficacy and tolerability of a fixed dose of BH-200 (250 mg BID) in outpatients with Major Depressive Disorder (MDD)

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Trial Profile

A 14-week, multicentre, double-blind, randomised, placebo-controlled phase II study with an 8-week treatment period to assess the efficacy and tolerability of a fixed dose of BH-200 (250 mg BID) in outpatients with Major Depressive Disorder (MDD)

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 12 Mar 2024

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At a glance

  • Drugs BH-200 (Primary)
  • Indications Major depressive disorder
  • Focus Proof of concept; Therapeutic Use
  • Acronyms OLIVE
  • Sponsors HMNC Brain Health
  • Most Recent Events

    • 20 Jun 2023 According to a MNC Brain Health media release, company announced that first patient has been enrolled.
    • 30 Mar 2023 Status changed from planning to recruiting.
    • 20 Oct 2022 According to an HMNC Brain Health media release, the company has raised an EUR 14.3 million in a funding series. These funds will be utilized in the development of the Nelivabon program, including this trial.

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