Clinical Research Directory

Key inclusion Criteria: 1. Histologically confirmed nodal T-follicular helper (TFH) cell lymphoma according to the 2022 WHO classification. 2. Previously untreated with systemic anti-lymphoma therapy. 3. Age ≥18 and \<75 years. 4. At least one measurable or evaluable lesion according to the Lugano 2014 criteria. 5. An expected survival time of more than 12 weeks. 6. An ECOG performance status score of 0-1. 7. Adequate organ and bone marrow function. 8. Provision of written informed consent and willingness to comply with all study procedures. Key exclusion Criteria: 1. Hemophagocytic syndrome. 2. Central nervous system or meningeal involvement by lymphoma. 3. Patients with a history of other malignancies within the past 5 years or concurrent malignancies, except for basal cell carcinoma of the skin. 4. Patients receiving potent CYP3A inducers or inhibitors, vitamin K antagonists, antiplatelet agents, or anticoagulants. 5. Patients with active infections, including tuberculosis, HIV infection, active hepatitis B, or active hepatitis C. 6. Patients with severe or uncontrolled cardiovascular disease. 7. Patients with a history of interstitial lung disease, except for asymptomatic radiation-induced interstitial lung disease. 8. Patients with gastrointestinal conditions that may interfere with oral administration or drug absorption. 9. Patients with known hypersensitivity to golidocitinib or its excipients. 10. Pregnant or breastfeeding women and participants of childbearing potential unwilling to use effective contraception. 11. Patients who have received systemic corticosteroids or other immunosuppressive therapy within 14 days before the start of study treatment. 12. Patients considered unsuitable for participation by the investigator.