CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 7 enrolled
Drug / intervention
BMS-901608 (Elotuzumab) 10 mg +1 morebiological
Likely dose
BMS-901608 (Elotuzumab) 10 mgfrom 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/NCT01241292
NCT01241292Phase 1Completed

Phase 1 Multiple Ascending Dose Study of Elotuzumab (BMS-901608) in Combination With Lenalidomide/Low-dose Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma in Japan

Bristol-Myers Squibb·interventional·Posted Nov 16, 2010·Updated Feb 15, 2018

In Brief

A Phase 1 clinical trial evaluating BMS-901608 (Elotuzumab) 10 mg and BMS-901608 (Elotuzumab) 20 mg for Multiple Myeloma. Completed, enrolled 7 participants across 3 sites.

Detailed Summary

The purpose of this study is to assess the safety and tolerability of Elotuzumab when given in combination with Lenalidomide and low-dose Dexamethasone in subjects with relapsed or refractory multiple myeloma (MM) in Japan.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan
Collaborators--

Timeline

Phase 1CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedNov 16, 2010
Enrollment StartJan 14, 2011
Primary CompletionFeb 14, 2014
Study CompletionJan 16, 2017
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 15.6 years ago

Interventions

BMS-901608 (Elotuzumab) 10 mgbiological

Injection, Intravenous, 10 mg/kg, Weekly at cycle 1 and 2, bi-weekly at cycle 3 and thereafter, Until disease progression or unacceptable toxicity became apparent

BMS-901608 (Elotuzumab) 20 mgbiological

Injection, Intravenous, 20 mg/kg, Weekly at cycle 1 and 2, bi-weekly at cycle 3 and thereafter, Until disease progression or unacceptable toxicity became apparent