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OncoMatch/Clinical Trials/NCT06768489

A Study of JNJ-79635322 in Combination With Daratumumab With or Without Lenalidomide or in Combination With Pomalidomide for Multiple Myeloma

Is NCT06768489 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including JNJ-79635322 and Daratumumab for multiple myeloma.

Phase 1RecruitingJanssen Research & Development, LLCNCT06768489Data as of May 2026

Treatment: JNJ-79635322 · Daratumumab · Pomalidomide · LenalidomideThe primary purpose of this study for Part 1 (Dose Escalation) is to identify the safe effective dose (recommended Phase 2 doses \[RP2Ds\]) and schedule for JNJ-79635322 treatment regimen in combination with daratumumab with or without lenalidomide or with pomalidomide; and for Part 2 (Dose Expansion) is to further characterize the safety and tolerability of JNJ-79635322 combination treatment regimens at selected RP2D(s).

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Cannot have received: targeted therapy

Targeted therapy ... within 21 days or 5 half-lives, whichever is less

Cannot have received: epigenetic therapy

epigenetic therapy ... within 21 days or 5 half-lives, whichever is less

Cannot have received: monoclonal antibody

monoclonal antibody (mAb) treatment ... within 21 days or 5 half-lives, whichever is less

Cannot have received: investigational drug

treatment with an investigational drug or an invasive investigational medical device within 21 days or 5 half-lives, whichever is less

Cannot have received: gene-modified adoptive cell therapy

Gene-modified adoptive cell therapy (example, chimeric antigen receptor [CAR] modified T cells, natural killer cells) within 90 days

Cannot have received: anti-CD38 directed therapy

Exception: for treatment regimen A only: within 90 days; for regimen B: within 21 days

Prior anti-CD38 directed therapy within 90 days (for treatment regimen A only; within 21 days for treatment regimen B)

Cannot have received: conventional chemotherapy

Conventional chemotherapy within 21 days

Cannot have received: proteasome inhibitor

PI therapy within 14 days

Cannot have received: immunomodulatory agent

Immunomodulatory agent therapy within 7 days

Cannot have received: radiation therapy

Radiotherapy within 14 days

Cannot have received: allogeneic stem cell transplant

Allogeneic stem cell transplant within 6 months before the first dose of study treatment

Cannot have received: autologous stem cell transplant

Exception: received less than or equal to (<=)12 weeks before the first dose of study treatment

Received an autologous stem cell transplant less than or equal to (<=)12 weeks before the first dose of study treatment

Cannot have received: CD3-redirecting therapy

Prior treatment with CD3-redirecting therapy

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

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