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Clinical Trial ● Currently Recruiting Phase III NCT07215585

AZD0486 1L Therapy for Elderly or Unfit Participants With LBCL

AZD0486 1L Therapy for Elderly or Unfit Participants With LBCL — Recruiting • Phase III • Oncology • NCT07215585.

📅 21 Apr 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07215585
Sponsor
AstraZeneca
Start
2025-11-11
ClinicaliQ Trial Snapshot
  • AZD0486 1L Therapy for Elderly or Unfit Participants With LBCL — Recruiting • Phase III • Oncology • NCT07215585.
  • What is being tested: The trial compares R-mini-CHOP chemotherapy (2 cycles) followed by AZD0486 versus standard R-mini-CHOP (6 cycles) as first-line treatment for large B-cell lymphoma (LBCL) in elderly or medically unfit patients.
  • Patient eligibility overview: The study focuses on newly diagnosed LBCL patients who are elderly or unfit for standard intensive chemotherapy regimens, representing a clinically vulnerable population with limited treatment options.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The purpose of this study is to measure the efficacy and safety of R-mini-CHOP × 2 followed by AZD0486 compared with R-mini-CHOP × 6 in elderly or unfit participants newly diagnosed with LBCL.

Eligibility Snapshot
  • : * Participants are either 80 years of age or older, OR 65 to 79 years of age or older and classified as unfit per sGA, and otherwise not considered candidates for full-dose R-CHOP per investigator assessment; * Histologically confirmed diagnosis of previously untreated LBCL as per WHO-HEM5 (excluding plasmablastic lymphoma) and follicular large cell lymphoma; * FDG-avid and measurable disease as per Lugano and Ann Arbor staging; * Stage I bulky (7.5 cm and greater) to Stage IV; * ECOG performance status 0 to 2; * Adequate bone marrow, liver, renal and cardiac function. The above is a summary, other inclusion criteria details may apply. * As judged by the investigator, any evidence of diseases which make it undesirable for the participant to participate in the study, or that would jeopardise compliance with the protocol * Diagnosis of post-transplant lymphoproliferative disease, plasmablastic lymphoma, Richter's transformation, prior history of or concurrent indolent lymphoma (including de novo transformed or composite lymphoma). * History of CNS involvement by their B-NHL or history of clinically relevant CNS medical condition * Known history of hemophagocytic lymphohistiocytosis/macrophage activation syndrome (HLH/MAS). * Active or uncontrolled infection * Major cardiac abnormalities * Prior anti-lymphoma therapy except…

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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