CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 395 enrolled
Drug / intervention
BMS-936558 (MDX-1106) +4 morebiological
Likely dose
BMS-936558 (MDX-1106) 0.1 mg/kgfrom 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/NCT00730639
NCT00730639Phase 1Completed

A Phase 1, Open-Label, Multicenter, Multidose, Dose Escalation Study of BMS-936558 (Nivolumab) in Subjects With Selected Advanced or Recurrent Malignancies

Bristol-Myers Squibb·interventional·Posted Aug 8, 2008·Updated Dec 3, 2021

In Brief

A Phase 1 clinical trial evaluating BMS-936558 (MDX-1106) for Metastatic Castration-resistant Prostrate Cancer and 3 related conditions. Completed, enrolled 395 participants across 13 sites.

Detailed Summary

The purpose of this study is to determine the safety and effectiveness of MDX-1106 in patients with certain types of cancer. Another purpose is to determine how MDX-1106 is absorbed and distributed within the body, and how it's eventually eliminated.

Study Details

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

Timeline

Phase 1CompletedFinished
2009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedAug 8, 2008
Enrollment StartOct 30, 2008
Primary CompletionFeb 4, 2013
Study CompletionDec 22, 2020
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 17.9 years ago

Interventions

BMS-936558 (MDX-1106)biological

Solution, Intravenous, 0.1 mg/kg - 10 mg/kg, Every 2 weeks, 3 years depending on response

BMS-936558 (MDX-1106)biological

Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response

BMS-936558 (MDX-1106)biological

Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response

BMS-936558 (MDX-1106)biological

Solution, Intravenous, 1 - 10 mg/kg, Every 2 weeks, 3 years depending on response

BMS-936558 (MDX-1106)biological

Solution, Intravenous, 10 mg/kg, Every 2 weeks, 3 years depending on response