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

Study acronym: TRIlogy-4
StatusRecruiting
PhasePhase 3
Started

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Record History

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  1. Notable Lead 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
  2. Minor Trial sites expanded: 124 → 144 locationsv12
  3. Minor Trial sites expanded: 109 → 124 locationsv11
  4. Notable Primary endpoint(s) modified
    • Trial sites expanded: 103 → 109 locations
    • Eligibility criteria shortened, about 17 words
    • Secondary endpoints revised (24)
    v10
  5. Minor Trial sites expanded: 65 → 103 locationsv9
  6. Minor Trial sites expanded: 43 → 65 locationsv8
  7. Minor Trial sites expanded: 39 → 43 locationsv7
  8. Minor Trial sites expanded: 33 → 39 locationsv6
  9. Minor Study sites: 10 to 33v5
  10. Minor Study sites: 9 to 10v4
  11. Notable Trial status: Not Yet Recruiting to Recruitingv3 Show 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
  12. Minor Re-verified, no change to tracked fieldsv2
  13. Minor Study 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.
Trial Details
NCT Number NCT07258511
Lead Sponsor Janssen Research & Development, LLC
Conditions
(from sponsor)
Multiple Myeloma
Related terms Multiple Myeloma
Enrollment 400 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov