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OncoMatch/Clinical Trials/NCT06855823

A Phase I/II Study of Golidocitinib Combined with Pomalidomide in R/R PTCL

Is NCT06855823 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies Golicitinib combined with Pomadomide for relapsed/refractory peripheral t-cell lymphoma (r/r ptcl).

Phase 1/2RecruitingSun Yat-sen UniversityNCT06855823Data as of May 2026

Treatment: Golicitinib combined with PomadomideThis is a phase I/II clinical trial to evaluate the efficacy and safety of Golidocitinib combined with Pomalidomide for relapsed/refractory peripheral T-cell lymphoma.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Performance status

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

Prior therapy

Min 1 prior line

Must have received: systemic therapy

Subjects must exhibit relapsed or refractory disease following prior systemic therapy, which may include autologous hematopoietic stem cell transplantation.

Cannot have received: allogeneic hematopoietic stem cell transplantation

Allogeneic hematopoietic stem cell transplantation prior to the administration of the investigational drug

Cannot have received: autologous hematopoietic stem cell transplantation

Exception: within six months preceding study drug administration

Autologous hematopoietic stem cell transplantation within six months preceding study drug administration

Cannot have received: golidocitinib (golidocitinib)

Previous use of golidocitinib

Cannot have received: pomalidomide (pomalidomide)

Previous use of pomalidomide

Cannot have received: cytotoxic chemotherapy

Exception: must not have been terminated within 21 days before the start of the study

Cytotoxic chemotherapy must not have been terminated within 21 days before the start of the study

Cannot have received: systemic antineoplastic therapy

Exception: within four weeks of study initiation

Received systemic antineoplastic therapy (including macromolecular monoclonal antibodies and immunotherapy drugs) within four weeks of study initiation

Cannot have received: radiation therapy

Exception: within three weeks

received radiation therapy within three weeks

Cannot have received: toxin/isotope-immune antibody conjugates

Exception: within ten weeks

Received other toxin/isotope-immune antibody conjugates within ten weeks

Cannot have received: experimental drug or investigational drug

Exception: within 30 days prior to study commencement

Received an experimental drug or investigational drug in another trial within 30 days prior to study commencement

Lab requirements

Blood counts

ANC ≥ 1.5×10^9/L; PLT ≥ 75×10^9/L (≥ 50×10^9/L with bone marrow infiltration); HB ≥ 80 g/L

Kidney function

serum creatinine (Scr) not exceeding 1.5x ULN

Liver function

serum total bilirubin (TBIL) not exceeding 1.5x ULN; ALT and AST not exceeding 2.5x ULN

Laboratory parameters must meet the following criteria: (1) absolute neutrophil count (ANC) of at least 1.5×10^9/L; (2) platelet count (PLT) of at least 75×10^9/L (with a minimum of 50×10^9/L for patients with bone marrow infiltration); (3) hemoglobin (HB) level of at least 80 g/L; (4) serum total bilirubin (TBIL) not exceeding 1.5 times the upper limit of normal (ULN); (5) alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels not exceeding 2.5 times the ULN; (6) serum creatinine (Scr) not exceeding 1.5 times the ULN.

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

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