A Study Comparing JNJ-79635322 and Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Janssen Research & Development, LLC
- Study ID
- NCT07518186
- 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 teclistamab.
Key Dates
- First listed
- Apr 8, 2026
- Start date
- May 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Apr 29, 2029
- Completion
- Dec 8, 2032
Study Design
- Enrollment
- 700 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm A: JNJ-79635322Participants will receive subcutaneous (SC) dose of JNJ-79635322 treatment of a finite duration or intolerable toxicity (whichever is first).
- Active Comparator: Arm B: TeclistamabParticipants will receive teclistamab as a SC injection until PD or intolerable toxicity.
Primary Outcome Measure
Complete Response (CR) or Better [ Time Frame: Up to approximately 41 months ]
Central Contacts
- Study Contact844-434-4210
Locations (35)
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