drugset / Trial / NCT05655507

Zuranolone Pharmacokinetics (PK) and Safety Study Adolescent Participants With Major Depressive Disorder (MDD)

NCT05655507

Phase 1 Completed 19 enrolled Biogen
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the pharmacokinetics and safety of Zuranolone in adolescents (ages 12 to 17 years) with MDD.

Timeline

Start
2023-04-19
Primary completion
2024-10-18
Completion
2024-10-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Zuranolone Small molecule 40 mg Oral
Subject Zuranolone Small molecule 50 mg Oral