CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 75 enrolled
Drug / intervention
MDX-010drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00323882
NCT00323882Phase 2Completed

A Phase I/II, Open-label, Dose-escalation Study of MDX-010 Administered Every 3 Weeks for 4 Doses in Patients With Metastatic Hormone-Refractory Prostate Cancer

Bristol-Myers Squibb·interventional·Posted May 10, 2006·Updated Aug 28, 2014

In Brief

A Phase 2 clinical trial evaluating MDX-010 for Prostate Cancer and Neoplasm Metastasis. Completed, enrolled 75 participants across 14 sites.

Detailed Summary

Multicenter study in which patients with metastatic hormone refractory prostate cancer (HRPC), who have not had previous chemotherapy or immunotherapy treatments, received MDX-010 every 3 weeks for 4 doses (12 weeks total duration of induction). MDX-010 was administered at escalating dosage levels of 3, 5, and 10 mg/kg/dose infusions. At least 6 patients were to be enrolled in each dosage level. Patients who tolerated and responded to treatment or who had stable disease for 3 months or longer and who subsequently progressed during the follow up phase of the study had the option to receive additional treatment with MDX-010, up to 4 cycles. Patients were followed in the study for response up to 2 years and were followed for survival status for up to 5 years after enrollment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 10, 2006
Enrollment StartJan 1, 2006
Primary CompletionSep 1, 2009
Study CompletionJul 1, 2013
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 20.1 years ago

Interventions

MDX-010drug

selected dose administered IV every 3 weeks