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OncoMatch/Clinical Trials/NCT06530550

PI3K Inhibitors for the Treatment of Relapsed/Refractory Indolent T/NK-cell Lymphomas

Is NCT06530550 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies PI3K inhibitor for lymphoma, t-cell.

Phase 2RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT06530550Data as of May 2026

Treatment: PI3K inhibitorIndolent T/NK-cell lymphomas are a heterogeneous group of lymphoproliferative diseases originating from T/NK cells, characterized by slow growth and proliferation, but currently remain incurable. For indolent T/NK-cell lymphomas that are unresponsive to first-line treatment, there are few treatment options available and the prognosis is poor. This study is an open-label, prospective clinical trial aimed at evaluating the feasibility, efficacy, and safety of PI3K inhibitors in the treatment of relapsed/refractory indolent T/NK-cell lymphomas. Patients will be treated with Linperlisib or Duvelisib, with an expected overall response rate of 60% for PI3K inhibitor treatment.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Prior therapy

Cannot have received: PI3K inhibitor

Subjects who have previously used any PI3K inhibitors

Cannot have received: autologous hematopoietic stem cell transplantation

Exception: within 90 days before the first dose of study treatment

Received autologous hematopoietic stem cell transplantation within 90 days before the first dose of study treatment

Cannot have received: allogeneic bone marrow or hematopoietic stem cell transplantation

history of allogeneic bone marrow or hematopoietic stem cell transplantation

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

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