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OncoMatch/Clinical Trials/NCT07123454

A Phase I/II Study of AZD4512 Monotherapy or in Combination With Anticancer Agents in Participants With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

Is NCT07123454 recruiting? Yes, currently enrolling (Sep 2026). This Phase 1/2 trial studies AZD4512 for b-cell non-hodgkin lymphoma.

Phase 1/2RecruitingAstraZenecaNCT07123454Data as of Sep 2026Location: International · 8 countries

Treatment: AZD4512This is a Phase I/II open-label, global multicenter study to evaluate the safety and efficacy of AZD4512 monotherapy or in combination with other anticancer agent(s), in participants with Relapsed/Refractory B-cell Non-Hodgkin Lymphoma (B-NHL).

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Extracted eligibility criteria

Treatments studied

Other

AZD4512

Cancer type

Non-Hodgkin Lymphoma

Performance status

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

Prior therapy

Min 2 prior lines

Must have received: systemic therapy — relapsed/refractory B-cell Non-Hodgkin Lymphoma

relapsed or refractory disease after at least two prior lines of systemic therapy and lack additional standard options with established benefit

Must have received: anti-CD20 therapy — LBCL

LBCL patients must have progressed after both anti-CD20 and at least one systemic chemotherapy regimen

Must have received: systemic chemotherapy — LBCL

LBCL patients must have progressed after both anti-CD20 and at least one systemic chemotherapy regimen

Must have received: anti-CD20 therapy — Mantle cell lymphoma

Mantle cell lymphoma (MCL) patients must have had anti-CD20 and Bruton's Tyrosine Kinase (BTK) inhibitor

Must have received: BTK inhibitor — Mantle cell lymphoma

Mantle cell lymphoma (MCL) patients must have had anti-CD20 and Bruton's Tyrosine Kinase (BTK) inhibitor

Lab requirements

Blood counts

adequate bone marrow function as specified by blood counts

Kidney function

adequate renal parameters as specified by protocol

Liver function

adequate hepatic parameters as specified by protocol

Cardiac function

adequate cardiac ejection fraction as specified by protocol

adequate organ and bone marrow function (as specified by blood counts, cardiac ejection fraction, renal and hepatic parameters, and coagulation indices)

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

US trial sites

  • Research Site · Myrtle Beach, South Carolina
  • Research Site · Franklin, Tennessee
  • Research Site · Irvine, California
  • Research Site · Jacksonville, Florida
  • Research Site · Rochester, Minnesota

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07123454 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received systemic therapy and anti-CD20 therapy.

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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