drugset / Trial / NCT04663321

Efficacy and Safety of MK-1942 When Added to Stable Antidepressant Therapy in Participants With Treatment-Resistant Depression (TRD) (MK-1942-006)

NCT04663321

Phase 2 Terminated 99 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to assess the efficacy and safety of daily and intermittent dosing of MK-1942 compared to placebo among participants with Treatment-Resistant Depression (TRD) on a stable course of antidepressant therapy. The dual primary hypotheses of the study are that the daily MK-1942 treatment or intermittent MK-1942 treatment are superior to placebo in reducing Montgomery-Asberg Depression Rating Scale (MADRS) score.

Timeline

Start
2021-05-20
Primary completion
2023-09-08
Completion
2023-09-08

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-1942 Unknown 10 mg Oral
Subject MK-1942 Unknown 20 mg Oral

Indications

No indication recorded.