Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL)

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Review clinical trials related to Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Dose Determining Study of EXS73565 in Participants With Relapsed or Refractory B-Cell Malignancies

The purpose of this study is to characterize the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of EXS73565 administered orally as a single agent in participants with relapsed/refractory B-cell malignancies.

Participants needed: 85
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.Updated: Jun 11, 2026Locations: 9
Eligibility criteria

Age ≥18 years at the time of signing the informed consent. [+3]

Any medical or psychiatric condition that, in the view of the Principal Investig... [+3]

Status: Not yet recruiting

A Study of Rocbrutinib in Combination With Lacutoclax in Patients With B-Cell Malignancies

BTK inhibitors and BCL-2 inhibitors have demonstrated significant clinical activity in mature B-cell malignancies, and combination therapy may provide improved clinical benefit. This is a multi-center, open-label, single-arm Phase Ib/II clinical study. The purpose of this clinical trial is to investigate the safety, tolerability, pharmacokinetics, and preliminary efficacy of Rocbrutinib, a fourth-generation Bruton tyrosine kinase inhibitor (BTKi), in combination with the BCL-2 inhibitor Lacutoclax in patients with mature B-cell malignancies. The Phase Ib will use a classic 3+3 dose-escalation design to evaluate dose-limiting toxicities (DLTs), determine the maximum tolerated dose (MTD), and identify the recommended dosing regimen. The Phase II portion is intended to further evaluate the efficacy and safety of the combination therapy.

Participants needed: 92
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Guangzhou Lupeng Pharmaceutical Company LTD.Updated: Jun 10, 2026
Eligibility criteria

Age ≥18 years, regardless of sex. [+7]

Known hypersensitivity or intolerance to Rocbrutinib, Lacutoclax, or any of thei... [+19]