RecruitingPhase IIEN originalLymphoma

Odronextamab for Relapsed and Refractory Large B-cell Lymphomas Before CAR-T

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This phase II trial tests the effectiveness of odronextamab given before chimeric antigen receptor T (CAR-T) cell therapy (bridging therapy) in patients with large B-cell lymphomas that have come back after a period of improvement (relapsed) or that have not responded to previous treatment (refractory). Odronextamab is a bispecific antibody that can bind to two different antigens at the same time. Odronextamab binds to CD3, a T-cell surface antigen, and CD20 (a tumor-associated antigen that is expressed on B-cells during most stages of B-cell development and is often overexpressed in B-cell cancers) and may interfere with the ability of cancer cells to grow and spread. Bridging therapy has been used to maintain disease control and to increase the chance of successful receipt of CAR-T cell therapy. However, bridging therapy is typically given after leukapheresis, which does not help prevent disease progression between the decision for CAR-T cell therapy and leukapheresis. Giving odronextamab as bridging therapy before leukapheresis may delay disease progression to allow leukapheresis and increase the likelihood of successful CAR-T cell therapy in patients with relapsed or refractory large B-cell lymphomas.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Potwierdzony chłoniak z dużych komórek B (DLBCL), chłoniak pierwotnie śródpiersiowy, wysoko-złośliwy chłoniak z komórek B lub chłoniak z komórek B powstały z wolno rosnących chłoniaków
  • •Mierzalne zmiany nowotworowe o wielkości co najmniej 15 mm widoczne w badaniu PET, CT lub MRI (zrobione w ciągu miesiąca przed badaniem)
  • •Niepowodzenie wcześniejszego leczenia pierwszej linii i kwalifikacja do terapii CAR-T (axicabtagene ciloleucel, lisocabtagene maraleucel lub tisagenlecleucel)
  • •Wiek co najmniej 18 lat
  • •Zdolność do zrozumienia i podpisania świadomej zgody
  • •Wcześniejsze leczenie lekami anty-CD20
  • •Dobry stan ogólny pacjenta (karność 0-1, w wyjątkowych przypadkach 2 jeśli wynika z choroby)
  • •Prawidłowa funkcja nerek, wątroby, płuc i serca oraz liczba krwinek w normie (lub bliska normie)

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
August 28, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Fred Hutch/University of Washington Cancer Consortium

Seattle, United States

Trial contact

Mengyang Di, MD, PhD

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/29/2026.

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