U.S., Feb. 21 -- ClinicalTrials.gov registry received information related to the study (NCT06836063) titled 'Study to Evaluate Efficacy and Safety of Ropanicant in MDD Patients' on Feb. 18.
Brief Summary: The primary objective is to evaluate the efficacy of Ropanicant at two different dosage levels compared to placebo in patients with Major Depressive Disorder (MDD).
Study Start Date: April 30
Study Type: INTERVENTIONAL
Condition:
Major Depressive Disorder (MDD)
Intervention:
DRUG: Ropanicant
Tablet dosage form, twice a day
DRUG: Placebo
Matching placebo tablets, twice a day
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Suven Life Sciences Limited
Disclaimer: Curated by HT Syndication....