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OncoMatch/Clinical Trials/NCT05652335

A Study of JNJ-79635322 in Participants With Relapsed or Refractory Multiple Myeloma or Previously Treated Amyloid Light-chain (AL) Amyloidosis

Is NCT05652335 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies JNJ-79635322 for relapsed or refractory multiple myeloma.

Phase 1RecruitingJanssen Research & Development, LLCNCT05652335Data as of May 2026

Treatment: JNJ-79635322The primary purpose of this study is to identify the recommended phase 2 dose (RP2D\[s\]) and schedule(s) to be safe for JNJ-79635322 in Part 1 (dose escalation), and to characterize the safety and tolerability of JNJ-79635322 at the RP2D(s) selected and in disease subgroups in Part 2 (dose expansion).

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 3 prior lines

Must have received: proteasome inhibitor

have been treated with a proteasome inhibitor

Must have received: immunomodulatory drug

have been treated with an immunomodulatory drug (IMiD) agent

Must have received: anti-CD38-based therapy

have been treated with an anti-CD38-based therapy

Cannot have received: proteasome inhibitor

PI therapy within 14 days prior to the first dose of study treatment

Cannot have received: immunomodulatory drug

IMiD agent therapy within 7 days prior to the first dose of study treatment

Cannot have received: gene-modified adoptive cell therapy

Exception: not applicable for Part 2C participants

gene-modified adoptive cell therapy within 90 days

Cannot have received: CD3-redirecting therapy

Exception: not applicable for Part 2B or 2C participants

CD3-redirecting therapy within 21 days

Cannot have received: radiation therapy

radiotherapy within 14 days

Cannot have received: allogeneic transplant

Prior allogeneic transplant within 6 months before the start of study treatment administration

Cannot have received: autologous transplant

autologous transplant within 12 weeks before the start of study treatment administration

Lab requirements

Cardiac function

left ventricular ejection fraction (lvef) >=45%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • City of Hope · Duarte, California
  • City of Hope Orange County Lennar Foundation Cancer Center · Irvine, California
  • University of California San Francisco · San Francisco, California
  • Colorado Blood Cancer Institute · Denver, Colorado
  • Icahn School of Medicine at Mt. Sinai · New York, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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