Clinical Trials · NCT01634321

The Clinical Trial to Evaluate the Efficacy and Safety of Luphere Depot Inj. 3.75mg(Leuprolide Acetate 3.75mg) in Patients With Precocious Puberty

CompletedPhase 4Gonadorelin (Approved)
Phase
Phase 4
Recruitment status
Completed
Sponsor
Daewoong Pharmaceutical Co. LTD.
Enrollment
63
Start date
Jul 2011
Locations
1 site, South Korea
Primary endpoint
At 24 weeks, percentage of subjects with suppression of peak-stimulated Luteinizing Hormone (LH) concentrations
View Gonadorelin compound reference