RecruitingPhase IIEN originalLeukemia

Nemtabrutinib and Lisocabtagene Maraleucel for the Treatment of Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

⚠️

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 studies how well the addition of nemtabrutinib to lisocabtagene maraleucel in treating patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory). Nemtabrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Lisocabtagene maraleucel is a type of treatment called chimeric antigen receptor (CAR) T-cell therapy, in which a patient's T-cells (a type of immune system cell) are changed in the laboratory so they will attack cancer cells. T-cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein on the patient's cancer cells is added to the T-cells in the laboratory. The special receptor is called a chimeric antigen receptor (CAR). Large numbers of the CAR T-cells are grown in the laboratory and given to the patient by infusion for treatment. Adding nemtabrutinib to lisocabtagene maraleucel may be an effective treatment for relapsed/refractory CLL/SLL.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Potwierdzona diagnoza białaczki limfocytowej przewlekłej lub chłoniaka limfocytowego
  • Widoczna choroba w badaniach obrazowych (powiększone węzły chłonne) lub podwyższona liczba limfocytów we krwi
  • Kwalifikacja do standardowego leczenia lisocabtagenu maraleucel według zaleceń FDA
  • Wiek co najmniej 18 lat
  • Zdolność przełykania i przyjmowania leków w postaci tabletek
  • Odpowiednie wyniki badań krwi (liczba neutrofili, hemoglobina, płytki krwi)
  • Pacjenci z wirusem zapalenia wątroby B mogą uczestniczyć po co najmniej 4 tygodniach leczenia przeciwwirusowego

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
July 10, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Fred Hutch/University of Washington Cancer Consortium

Seattle, United States

Trial contact

Fred Hutch Immunotherapy Intake

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/11/2026.

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