CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 230 target
Drug / intervention
Arlocabtagene Autoleucelbiological
Likely dose
Not stated in record
Key inclusion· 6
  • Documented diagnosis of multiple myeloma per IMWG criteria
  • At least 4 classes of MM treatment including IMiD, PI, anti-CD38 mAb, anti-BCMA therapy
  • At least 3 prior lines of therapy
  • Documented disease progression during or after last anti-myeloma regimen per IMWG 2016 criteria
Key exclusion· 4
  • Active or history of CNS involvement with MM
  • Active systemic fungal, bacterial, viral, or other infection despite appropriate treatment at leukapheresis
  • Severe infection, severe sepsis, or bacteremia within 28 days prior to leukapheresis
  • Prior GPRC5D-directed therapy without required washout

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

Search/NCT06297226
NCT06297226Phase 2RecruitingHigh Momentum

A Phase 2, Open-Label, Multicenter Study of Arlocabtagene Autoleucel (BMS-986393), a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma (QUINTESSENTIAL)

Juno Therapeutics, Inc., a Bristol-Myers Squibb Company·interventional·Posted Mar 7, 2024·Updated May 28, 2026

In Brief

A Phase 2 clinical trial evaluating Arlocabtagene Autoleucel for Multiple Myeloma. Currently recruiting, targeting 230 participants across 52 sites in 4 countries.

Signals

Enrolling ahead of pace

Detailed Summary

The purpose of this study is to evaluate the effectiveness and safety of Arlocabtagene Autoleucel (BMS-986393) in participants with relapsed or refractory multiple myeloma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, Japan, United States
Collaborators--

Timeline

Phase 2Recruiting
202420252026202720282029203020312032
First PostedMar 7, 2024
Enrollment StartMar 21, 2024
Primary CompletionJun 30, 2027
Study CompletionJun 30, 2032
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 2.3 years agoPrimary completion in 12 months

Interventions

Arlocabtagene Autoleucelbiological

Specified dose on specified days