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Get research updatesThis historical record does not confirm current site availability.
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
This study is for people with depression. Other eligibility criteria apply.
This is historical registry information. What is the current study status and protocol?
A multicenter, Double-blind 58 week Rollover Study to assess the Safety and Tolerability of BMS-820836 in Patients with Treatment Resistant Major Depression.
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Austria · Finland · Italy
A listed location does not confirm current availability.
The study sponsor is Bristol-Myers Squibb International Corporation.
This study is for people with depression. Other eligibility criteria apply.
The historical registry lists this study as suspended.
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