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Study details
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A Study Comparing JNJ-79635322 and an Anti-B-cell Maturation Antigen (BCMA)xCD3 Bispecific Antibody in Participants With Relapsed or Refractory Multiple Myeloma

Janssen Research & Development, LLC
NCT IDNCT07258511ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Ages

18+

Locations

15 sites in CA, CT, FL +7

About this study

This Phase 3 study is testing Teclistamab in people with multiple myeloma. The primary outcome being measured is Overall Response Rate (ORR).

Based on ClinicalTrials.gov records.

PhasePhase 3
DrugTeclistamab
Primary goalOverall Response Rate (ORR)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low7%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

teclistamab

Endpoints

Primary: Overall Response Rate (ORR), Progression-Free Survival (PFS)

Secondary: Change from Baseline in Symptoms, Functioning, and HRQoL as Assessed by European Organization for Research and Treatment of Cancer Quality of life Questionnaire Core 30 (EORTC-QLQ-C30) Score, Change from Baseline in Symptoms, Functioning, and HRQoL as Assessed by European Quality of Life 5-Dimensions 5-Level Version (EQ-5D-5L) Score, Change from Baseline in Symptoms, Functioning, and Health-related Quality of Life (HRQoL) as Assessed by Multiple Myeloma Symptom and Impact Questionnaire (MySIm-Q) Score, Complete Response (CR) or Better, Duration of Response (DoR), MRD-negative CR at 9 months, Minimal Residual Disease (MRD)-negative CR, Number of Participants With Treatment-Emergent Adverse Events (TEAE) by Severity

Body systems

Oncology