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OncoMatch/Clinical Trials/NCT05602363

AS-1763 in Patients With Previously Treated CLL/SLL or Non-Hodgkin Lymphoma

Is NCT05602363 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Docirbrutinib for b-cell malignancy.

Phase 1RecruitingCarna Biosciences, Inc.NCT05602363Data as of May 2026

Treatment: DocirbrutinibThis is an open-label, multi-center Phase 1b clinical study of oral AS-1763 (docirbrutinib) in patients with CLL/SLL or B-cell NHL who have failed or are intolerant to ≥2 lines of systemic therapy.

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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

Min 2 prior lines

Cannot have received: docirbrutinib (docirbrutinib)

Prior treatment with docirbrutinib

Cannot have received: noncovalent BTK inhibitor

Exception: pirtobrutinib (Jaypirca) allowed in Dose Expansion Cohort 3

Dose Escalation and Cohort 3 patients: prior treatment with noncovalent BTKi except pirtobrutinib (Jaypirca); Dose Expansion Cohort 1 and Cohort 2 patients: prior treatment with any noncovalent BTKi

Lab requirements

Blood counts

absolute neutrophil count ≥0.75 × 10⁹/L, platelet count ≥50 × 10⁹/L, hemoglobin ≥8 g/dL not requiring transfusion support or growth factors

Kidney function

Adequate renal function

Liver function

Adequate hepatic function

Cardiac function

No clinically significant, uncontrolled cardiac, cardiovascular disease or history of myocardial infarction within 6 months before planned start of docirbrutinib, or prolongation of the QT interval corrected for heart rate using Fridericia's Formula (QTcF) >470 msec on at least 2 of 3 consecutive ECGs, and mean QTcF >470 msec on all 3 ECGs, during Screening

Adequate hematologic status (ie, absolute neutrophil count ≥0.75 × 10⁹/L, platelet count ≥50 × 10⁹/L, hemoglobin ≥8 g/dL) not requiring transfusion support or growth factors; Adequate hepatic function; Adequate renal function; ... history of myocardial infarction within 6 months ... or prolongation of the QT interval ... QTcF >470 msec

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

US trial sites

  • UC Irvine Health · Orange, California
  • Mount Sinai Comprehensive Cancer Center · Miami Beach, Florida
  • Moffitt Cancer Center · Tampa, Florida
  • Northwestern Memorial Hospital · Chicago, Illinois
  • American Oncology Partners · Fort Wayne, Indiana

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

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