Project Details
Description
A Phase 3, Multicenter, Open-Label, Two-Part Study to Evaluate the Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of Leuprolide Acetate 45 mg 6-month formulation in Children with Central Precocious Puberty (CPP)
Status | Finished |
---|---|
Effective start/end date | 11/1/18 → 9/30/23 |
Funding
- ABBVIE INC
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