At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 2, Randomized, Non-Comparative, Two-Arm Open Label, Multiple-Center Study Of CP-751,871 In Combination With Docetaxel/Prednisone In Chemotherapy- Naive (Arm A) And Docetaxel/Prednisone Refractory (Arm B) Patients With Hormone Insensitive Prostate Cancer
In Brief
A Phase 2 clinical trial evaluating CP-751,871, docetaxel, and 1 other intervention for Prostatic Neoplasms. Completed, enrolled 204 participants across 18 sites in 6 countries.
Detailed Summary
To test the efficacy of CP-751,871 combined with docetaxel and prednisone in the treatment of prostate cancer that is refractory to hormone therapy
Study Details
Timeline
Interventions
CP-750,871 is administered intravenously at a dose of 20 mg/kg on day 1 of each 21-day cycle (for patient convenience and logistical management, the dose of CP-751,871 may be deferred up to 7 days).
Docetaxel is administered IV on day 1 of each 21-day cycle, at a dose of 75 mg/m2.
Prednisone is administered at a dose of 5 mg twice daily.
Docetaxel is administered IV on day 1 of each 21-day cycle, at a dose of 75 mg/m2.
Prednisone is administered at a dose of 5 mg twice daily.