Phase 4Completed

A Study To Assess The Safe-Use Conditions For Administration of ZULRESSO® in a Home Setting

Assessment of Safe-use Conditions for Administration of ZULRESSO in a Home Setting

Sponsor
Supernus Pharmaceuticals, Inc. (Industry)
Enrollment
52 enrolled
Conditions
Postpartum Depression
Interventions
ZULRESSO®
Ages
adults, older adults
Registry
NCT05059600

Full record on ClinicalTrials.gov

From the registry

The primary purpose of this study was to evaluate whether the safe-use conditions for administration of brexanolone (ZULRESSO®) can be implemented in a home setting.

Primary outcomes

  • Percentage of Participants With At Least One Treatment-Emergent Adverse Event (TEAE) Leading to Dose Interruption/Discontinuation

History

  1. Last registry update

  2. Results first posted

  3. Primary completion

  4. Started

  5. Registered