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).
Treatment: Golicitinib combined with Pomadomide — This 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.
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Hodgkin Lymphoma
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
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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