CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 681 enrolled
Drug / intervention
Ipilimumab +2 moredrug
Likely dose
Ipilimumab 10mg/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/NCT00324155
NCT00324155Phase 3Completed

A Multi-center, Randomized, Double-Blind, Two-Arm, Phase III Study in Patients With Untreated Stage III (Unresectable) or IV Melanoma Receiving Dacarbazine Plus 10 mg/kg Ipilimumab (MDX-010) vs. Dacarbazine With Placebo

Bristol-Myers Squibb·interventional·Posted May 10, 2006·Updated Nov 3, 2014

In Brief

A Phase 3 clinical trial evaluating Ipilimumab, Placebo, and 1 other intervention for Melanoma. Completed, enrolled 681 participants across 127 sites in 25 countries.

Detailed Summary

The purpose of this clinical research study is to examine the safety and effectiveness (how well the drug works) of two different treatments for patients with melanoma. One treatment is an investigational compound (a drug that is not currently approved by the United States Food and Drug Administration \[FDA\]), know as Ipilimumab (also known as MDX-010 or BMS-734016) together with an approved chemotherapy drug called Dacarbazine

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMelanoma
CountriesArgentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Czechia, France, Germany, Hungary, Ireland, Israel, Italy, Netherlands, Norway, Poland, Portugal, Russia, South Africa, Spain, Switzerland, Ukraine, United Kingdom, United States
CollaboratorsMedarex

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 10, 2006
Enrollment StartAug 1, 2006
Primary CompletionJan 1, 2011
Study CompletionOct 1, 2013
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 20.1 years ago

Interventions

Ipilimumabdrug

Intravenous solution; intravenous; 10mg/kg; one dose every 3 weeks for 10 weeks then one dose every 12 weeks starting at Week 24, until disease progression, unacceptable toxicity or withdrawal of consent In Maintenance phase: Only Ipilimumab: 10mg/kg, every 12 weeks will be continued until disease progression

Placebodrug

Intravenous solution; intravenous; 0 mg; one dose every 3 weeks for 10 weeks then one dose every 12 weeks starting at Week 24; until disease progression, unacceptable toxicity or withdrawal of consent

Dacarbazinedrug

Intravenous solution; intravenous; 850 mg/m\^2; one dose every 3 weeks for 22 weeks, until disease progression, unacceptable toxicity or withdrawal of consent