A Study Comparing JNJ-79635322 and an Anti-B-cell Maturation Antigen (BCMA)xCD3 Bispecific Antibody in Participants With Relapsed or Refractory Multiple Myeloma
NotableLead sponsor: Janssen Research & Development, LLC to Janssen Research & Development, LLC
Trial sites expanded: 144 → 150 locations
Eligibility criteria expanded, about 12 words
Secondary endpoints: details revised at 14 of 24 entries
MinorTrial sites expanded: 124 → 144 locationsv12
MinorTrial sites expanded: 109 → 124 locationsv11
NotablePrimary endpoint(s) modified
Trial sites expanded: 103 → 109 locations
Eligibility criteria shortened, about 17 words
Secondary endpoints revised (24)
v10
MinorTrial sites expanded: 65 → 103 locationsv9
MinorTrial sites expanded: 43 → 65 locationsv8
MinorTrial sites expanded: 39 → 43 locationsv7
MinorTrial sites expanded: 33 → 39 locationsv6
MinorStudy sites: 10 to 33v5
MinorStudy sites: 9 to 10v4
NotableTrial status: Not Yet Recruiting to Recruitingv3Show 4 more changesShow less
Study sites: 0 to 9
Start date changed from estimate of Feb 20, 2026 to Feb 4, 2026
Secondary endpoints: details revised at 1 of 24 entries
Eligibility criteria expanded, about 1 word
MinorRe-verified, no change to tracked fieldsv2
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.