RecruitingPhase IEN originalLymphoma

Testing the Combination of Anti-cancer Drugs Mosunetuzumab, Polatuzumab Vedotin, and Lenalidomide for the Treatment of Relapsed/Refractory Diffuse Large B-Cell Lymphoma

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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 I trial studies the side effects and best dose of mosunetuzumab when given together with polatuzumab vedotin and lenalidomide in treating patients with diffuse large B-cell lymphoma (DLBCL) that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). Mosunetuzumab and polatuzumab vedotin are monoclonal antibodies that may interfere with the ability of cancer cells to grow and spread. Polatuzumab, linked to a toxic agent called vedotin, attaches to CD79B positive cancer cells in a targeted way and delivers vedotin to kill them. Lenalidomide may stimulate or suppress the immune system in different ways and stop cancer cells from growing and by preventing the growth of new blood vessels that cancer cells need to grow. Giving mosunetuzumab with polatuzumab vedotin and lenalidomide may work better in treating patients with relapsed/refractory DLBCL.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Pacjent ma potwierdzonego chłoniaka rozlanego z dużych komórek B (DLBCL) lub podobny typ chłoniaka.
  • Choroba powróciła lub nie zareagowała na wcześniejsze leczenie.
  • Pacjent może był leczony wcześniej lekiem polatuzumab vedotin.
  • Choroba jest widoczna w badaniach obrazowych (np. tomografia komputerowa lub PET) i ma co najmniej jeden wymiar powyżej 1,5 cm.
  • Pacjent ma ukończone 18 lat.
  • Stan ogólny pacjenta pozwala na udział w badaniu (nie jest zbyt osłabiony).
  • Przewidywana długość życia pacjenta wynosi co najmniej 12 tygodni.
  • Wyniki badań krwi wskazują na odpowiednią liczbę białych krwinek, płytek krwi i hemoglobiny.

✗ Disqualifies

  • Pacjenci poniżej 18 roku życia są wykluczeni, ponieważ brak danych o stosowaniu tych leków u dzieci.
  • Pacjenci, których choroba bardzo szybko się rozwija lub są w bardzo złym stanie ogólnym mogą zostać wykluczeni.

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
July 9, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (8)

City of Hope Comprehensive Cancer Center

Duarte, United States

University of California Davis Comprehensive Cancer Center

Sacramento, United States

Moffitt Cancer Center

Tampa, United States

Northwestern University

Chicago, United States

Wake Forest University Health Sciences

Winston-Salem, United States

Case Western Reserve University

Cleveland, United States

University of Oklahoma Health Sciences Center

Oklahoma City, United States

University of Virginia Cancer Center

Charlottesville, United States

Trial contact

Geoffrey Shouse

PRINCIPAL_INVESTIGATOR

Site Public Contact

Joseph M. Tuscano

PRINCIPAL_INVESTIGATOR

Bijal D. Shah

PRINCIPAL_INVESTIGATOR

Reem Karmali

PRINCIPAL_INVESTIGATOR

Site Public Contact

Rakhee Vaidya

PRINCIPAL_INVESTIGATOR

Changchun Deng

PRINCIPAL_INVESTIGATOR

Sami Ibrahimi

PRINCIPAL_INVESTIGATOR

Emily Ayers

PRINCIPAL_INVESTIGATOR

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/8/2026.

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