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 (May 2026). This Phase 1/2 trial studies AZD4512 for b-cell non-hodgkin lymphoma.
Treatment: AZD4512 — This 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).
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Hodgkin Lymphoma
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: anti-CD20 therapy — LBCL, MCL, FL
LBCL patients must have progressed after both anti-CD20 and at least one systemic chemotherapy regimen; MCL patients must have had anti-CD20; FL patients should have failed anti-CD20
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: CAR-T cell therapy — LBCL
LBCL patients must have considered or be ineligible for CAR-T, T cell engager, and stem cell transplant modalities
Must have received: T cell engager — LBCL
LBCL patients must have considered or be ineligible for CAR-T, T cell engager, and stem cell transplant modalities
Must have received: stem cell transplant — LBCL
LBCL patients must have considered or be ineligible for CAR-T, T cell engager, and stem cell transplant modalities
Must have received: Bruton's Tyrosine Kinase (BTK) inhibitor — MCL
MCL patients must have had anti-CD20 and Bruton's Tyrosine Kinase (BTK) inhibitor
Cannot have received: CAR-T cell therapy
Exception: within 90 days prior to Cycle 1 Day 1 (C1D1)
received Chimeric antigen receptor-T (CAR-T) or T cell engager therapies within 90 days prior to Cycle 1 Day 1 (C1D1)
Cannot have received: T cell engager
Exception: within 90 days prior to Cycle 1 Day 1 (C1D1)
received Chimeric antigen receptor-T (CAR-T) or T cell engager therapies within 90 days prior to Cycle 1 Day 1 (C1D1)
Cannot have received: investigational drug
Exception: within 21 days or 5 half-lives
any investigational drug or other systemic anticancer therapies (except low-dose corticosteroids) within 21 days or 5 half-lives
Cannot have received: systemic anticancer therapy
Exception: within 21 days or 5 half-lives
any investigational drug or other systemic anticancer therapies (except low-dose corticosteroids) within 21 days or 5 half-lives
Cannot have received: curative radiation
Exception: within 14 days
curative radiation within 14 days (localized palliative radiotherapy is allowed)
Cannot have received: allogeneic Hematopoietic stem cell transplantation
Exception: within 180 days (unless stable without active GVHD for ≥2 months)
allogeneic Hematopoietic stem cell transplantation (HSCT) within 180 days (unless stable without active (graft-versus-host disease) GVHD for ≥2 months)
Cannot have received: autologous Hematopoietic stem cell transplantation
Exception: within 90 days (unless resolved toxicities)
autologous HSCT within 90 days (unless resolved toxicities)
Lab requirements
Blood counts
adequate bone marrow function as specified by protocol
Kidney function
adequate renal function as specified by protocol
Liver function
adequate hepatic function 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 · Irvine, California
- Research Site · Jacksonville, Florida
- Research Site · Rochester, Minnesota
- Research Site · New York, New York
- Research Site · New York, New York
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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