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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 (Jun 2026). This Phase 1 trial studies multiple treatments including JNJ-79635322 and Daratumumab for multiple myeloma.

Phase 1RecruitingJanssen Research & Development, LLCNCT06768489Data as of Jun 2026Location: International · 4 countries

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

Treatments studied

Immunotherapy

Daratumumab

Endocrine / hormonal

PomalidomideLenalidomide

Other

JNJ-79635322

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.

Frequently asked questions

Is NCT06768489 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior targeted therapy, epigenetic therapy, monoclonal antibody disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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