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OncoMatch/Clinical Trials/NCT05147467

Study of APG-2575 in Patients With Relapsed/Refractory CLL/SLL

Is NCT05147467 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies APG2575 for chronic lymphocytic leukemia.

Phase 2RecruitingAscentage Pharma Group Inc.NCT05147467Data as of Jun 2026Location: China

Treatment: APG2575The purpose of this study is to assess the efficacy and safety of APG-2575 single agent in patients with relapsed/refractory CLL/SLL.

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Extracted eligibility criteria

Treatments studied

Other

APG2575

Cancer type

Chronic Lymphocytic Leukemia

Performance status

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

Prior therapy

Min 1 prior line

Must have received: BTK inhibitor — refractory, recurrent, or intolerant

Refractory, recurrent, or intolerant to BTK inhibitors

Must have received: immunochemotherapy — refractory, recurrent, or intolerant

Refractory, recurrent, or intolerant to...immunochemotherapy

Cannot have received: BCL2 inhibitor

Received Bcl-2 inhibitor treatment

Cannot have received: allogeneic hematopoietic stem cell transplantation

Exception: if within 24 months

Prior history of allogeneic hematopoietic stem cell transplantation...within 24 months

Cannot have received: autologous hematopoietic stem cell transplantation

Exception: if within 24 months

Prior history of...autologous hematopoietic stem cell transplantation within 24 months

Cannot have received: adoptive cell immunotherapy

Exception: if within 24 months

Prior history of...adoptive cell immunotherapy...within 24 months

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

Frequently asked questions

Is NCT05147467 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior BCL2 inhibitor, allogeneic hematopoietic stem cell transplantation, autologous hematopoietic stem cell transplantation disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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