A Study Comparing JNJ-79635322 and an Anti-B-cell Maturation Antigen (BCMA)xCD3 Bispecific Antibody in Participants With Relapsed or Refractory Multiple Myeloma
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Janssen Research & Development, LLC
- Study ID
- NCT07258511
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- JNJ-79635322 — DRUGJNJ-79635322 will be administered as SC injection.
- Teclistamab — DRUGTeclistamab will be administered as SC injection.
Study Details
The purpose of this study is to evaluate how well JNJ-79635322 works when compared with an anti-B-cell maturation antigen (BCMA)xCD3 bispecific antibody.
Key Dates
- Start date
- Feb 4, 2026
- Status verified
- Jun 2026
- Primary completion
- Dec 12, 2028
- Completion
- Sep 30, 2031
Study Design
- Enrollment
- 400 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: JNJ-79635322Participants will receive subcutaneous (SC) dose of JNJ-79635322 until progressive disease (PD) or intolerable toxicity.
- Active Comparator: Anti BCMAxCD3 Bispecific AntibodyParticipants will receive teclistamab (an Anti BCMAxCD3 bispecific anitbody) as a SC injection until PD or intolerable toxicity.
Primary Outcome Measure
Overall Response Rate (ORR) [ Time Frame: Up to 5 years and 4 months ]
Central Contacts
- Study Contact844-434-4210
Locations (23)
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