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Clinical Trials · NCT00444639

Study to Assess the Non-inferiority of Pamorelin® 11,25mg SC Injected Versus Pamorelin® 11,25mg IM Injected in Patients Suffering From Advanced Prostate Cancer (PAMOJECT)

TerminatedPhase 2Gonadorelin (Prohibited)
Phase
Phase 2
Recruitment status
Terminated
Sponsor
Ipsen
Enrollment
25
Start date
Feb 2007
Locations
15 sites, Netherlands
Primary endpoint
Percentage of patients achieving a plasma testosterone level ≤ 50 ng/dl (1,7 nmol/l).
View Gonadorelin compound reference