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OncoMatch/Clinical Trials/NCT06716658

JAK1 Inhibitor Golidocitnib for the Treatment of Relapsed/Refractory Indolent T/NK-cell Lymphomas

Is NCT06716658 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies JAK1 Inhibitor for lymphoma, t-cell.

Phase 2RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT06716658Data as of May 2026

Treatment: JAK1 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 Golidocitnib, with an expected overall response rate of 60% for JAK1 inhibitor Golidocitnib treatment.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Performance status

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

Prior therapy

Min 1 prior line

Must have received: systemic therapy

lymphoma that has failed at least one systemic therapy or is intolerant to such treatment and/or currently has no effective standard treatment options

Cannot have received: JAK inhibitor

Subjects who have previously used any JAK inhibitors

Cannot have received: autologous hematopoietic stem cell transplantation

Exception: within 90 days prior to the first dose of study treatment

Subjects who have undergone autologous hematopoietic stem cell transplantation within 90 days prior to the first dose of study treatment

Lab requirements

Kidney function

blood urea nitrogen (bun)/urea and creatinine (cr) ≤ 1.5 × uln

Liver function

total bilirubin (tbil) ≤ 1.5 × uln; alt and ast ≤ 2.5 × uln

Cardiac function

left ventricular ejection fraction (lvef) ≥ 50%; fridericia-corrected qt interval (qtcf): < 450 ms for males, < 470 ms for females

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

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