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OncoMatch/Clinical Trials/NCT04505254

Acalabrutinib and Obinutuzumab for the Treatment of Chronic Lymphocytic Leukemia

Is NCT04505254 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Obinutuzumab and Acalabrutinib for chronic lymphocytic leukemia.

Phase 2RecruitingM.D. Anderson Cancer CenterNCT04505254Data as of May 2026

Treatment: Acalabrutinib · ObinutuzumabThis phase II trial investigates the how well acalabrutinib and obinutuzumab work in treating patients with chronic lymphocytic leukemia (CLL). Acalabrutinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with obinutuzumab may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread. Giving acalabrutinib and obinutuzumab may help to control disease progression in CLL patients who have not received treatment for CLL.

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Extracted eligibility criteria

Cancer type

Chronic Lymphocytic Leukemia

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: cll/sll treatment

Lab requirements

Blood counts

Absolute neutrophil count ≥ 500/μL (unless disease-related); platelet count ≥ 30,000/μL at screening

Kidney function

Estimated creatinine clearance (CrCl) > 30 mL/min, unless disease related

Liver function

Total bilirubin ≤ 1.5 x ULN except for Gilbert's disease; ALT ≤ 2.5 x ULN

Adequate renal and hepatic function as indicated by all of the following: Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN) except for patients with bilirubin elevation due to Gilbert's disease who will be allowed to participate; ALT ≤ 2.5 x ULN; estimated creatinine clearance (CrCl) > 30 mL/min, as calculated by the Cockcroft-Gault equation unless disease related; severe hematopoietic insufficiency as defined by an absolute neutrophil count of less than 500/μL, unless disease-related, and/or a platelet count of less than 30,000/μL at time of screening for this protocol.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • M D Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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