Medication described in the protocol · Medication and placebo comparator listed across study groups
Compensation
Payment and expense reimbursement have not been verified.
What to know before participating
A point to clarify
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Study clarity
Things to check before joining
Study start dateStarted: May 20, 2021
Recruitment status
Terminated
Enrollment listed in the registry
99
Sponsor
Merck Sharp & Dohme LLC
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT04663321
Official title
Show the full official title
A Phase 2a, Randomized, Placebo-Controlled Clinical Study to Evaluate the Efficacy and Safety of MK-1942 Added to Stable Antidepressant Therapy in Participants With Treatment-Resistant Depression
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Study ID: NCT04663321. We help you review the study, but cannot decide medical eligibility.
Recruitment & locations
Terminated
Birmingham · Little Rock · Bellflower
40 more locations
Colton
Garden Grove
Santa Ana
Hartford
Fort Myers
Hallandale
Jacksonville
Lauderhill
Miami
Naples
Orlando
Tampa
Winter Park
Atlanta
Decatur
Marietta
Savannah
Chicago
Gaithersburg
Boston
Ann Arbor
Las Vegas
Berlin
Princeton
Albuquerque
New York
Staten Island
Charlotte
Hickory
North Canton
Oklahoma City
Media
Philadelphia
Plymouth Meeting
Houston
Plano
Draper
Woodstock
Bellevue
Everett
A listed location does not confirm current availability.
FAQ
Questions about this study
What is this study about?
This study evaluates the safety and effectiveness of MK-1942 for people with depression.
Who is behind this study?
The study sponsor is Merck Sharp & Dohme LLC.
Does this study involve medication?
Yes. The study involves medication, including MK-1942 and Placebo.
Who can participate?
This study is for people with depression. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.
Is this study still recruiting?
The registry lists this study as terminated.
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