8 Week Multi-site Study of MYDAYIS® for Bipolar Depression

Completed · Phase 2 · Has a placebo group

Conditions studied: Bipolar Depression

In brief

This protocol is a Phase 2 multi-site study which aims to evaluate the safety and effectiveness of MYDAYIS\® as adjunctive therapy for adults with bipolar depression. Results from this study WILL NOT be used to contribute to an approval of MYDAYIS \® for this indication.

Key facts

Study ID
NCT04235686
Run by
Mayo Clinic
People needed
74
Starts
2020-07-17
Expected to finish
2025-07-25
Last updated by the study team
2025-08-12

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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