Relapsed/Refractory Peripheral T-Cell Lymphoma

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Review clinical trials related to Relapsed/Refractory Peripheral T-Cell Lymphoma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Clinical Study on Anti-PD-1 Plus Lenalidomide and Azacitidine in Relapsed/Refractory Peripheral T-cell Lymphoma

Aim of this study will evaluate the Efficacy and Safety of Anti-PD-1 monoclonal antibody Combined Lenalidomide and Azacitidine in Relapsed/Refractory Peripheral T-cell Lymphoma Patients.

Participants needed: 31
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Soochow UniversityUpdated: May 1, 2026Locations: 1
Eligibility criteria

Pathological immunohistochemistry or flow cytometry confirmed that R/R PTCL with... [+6]

Accepted major surgery within 4 weeks before treatment. [+8]

Status: Recruiting

Exploratory Clinical Study of SHR-0302 and SHR-2554 in Patients With Relapsed/Refractory Peripheral T Cell Lymphoma

This is an open-label, prospective and exploratory clinical study to evaluate the efficacy and safety of JAK inhibitor SHR-0302 in combination with EZH2 inhibitor SHR-2554 in patients with R/R PTCL. The study plans to enroll approximately 25 patients. 6-12 patients will receive SHR-0302 monotherapy and SHR-0302+SHR-2554 combination therapy in the safety run-in phase. According to the safety observed, the investigators discuss and decide to select a dose group to explore the efficacy and safety. 13 patients may be enrolled in the expansion phase.

Participants needed: 25
Trial details
Phase: Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Fudan UniversityUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Males or females aged 18-70 years (inclusive); [+7]

Received anti-tumor treatment within 28 days prior to the first dose of the stud... [+11]

Status: Recruiting

A Randomized, Double-blind, Multicenter Phase III Study of XNW5004 Tablets in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma

This is a randomized, double-blind, multi-center, phase III clinical trial designed to evaluate the efficacy of XNW5004 tablets versus Chidamide in Relapsed/Refractory PTCL, with a target of enrolling 120 subjects.

Participants needed: 120
Trial details
Phase: Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: Evopoint Biosciences Inc.Updated: Jan 9, 2026Locations: 1
Eligibility criteria

Aged 18-70 years (inclusive),gender not limited. [+10]

Prior exposure to EZH2 inhibitor(s) or EZH1/2 inhibitor(s). [+33]

Status: Not yet recruiting

To Evaluate XNW5004 Tablets in Patients with Relapsed or Refractory Peripheral T Cell Lymphoma

This is an open-label, multi-center clinical study to evaluate the efficacy and safety of XNW5004 tablets in subjects with R/R PTCL. The study plans to enroll approximately 50 subjects.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Evopoint Biosciences Inc.Updated: Nov 25, 2024
Eligibility criteria

Aged 18-70 years (inclusive),gender not limited. [+10]

Prior exposure to EZH2 inhibitor(s) or EZH1/2 inhibitor(s); [+33]