Azacitidine Plus PD-1 Therapy for Relapsed/Refractory Hodgkin Lymphoma
| Registry | NCT06190067 |
|---|---|
| Status | Recruiting |
| Phase | Phase 2 |
| Study type | Interventional; na, single group, masking: none, treatment |
| Enrollment | 40 (Estimated) |
| Sponsor | Navy General Hospital, Beijing (Other) |
| Conditions | Relapsed Classic Hodgkin Lymphoma, Refractory Classic Hodgkin Lymphoma |
| Interventions | Azacitidine Plus PD-1 therapy (Drug) |
| Dates | start 2023-10-30, primary completion 2026-12-01 (estimated), completion 2028-12-01 (estimated), first posted 2024-01-05, last updated 2024-01-30 |
| Locations | 1 site in China |
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All trials for Relapsed Classic Hodgkin Lymphoma All trials for Refractory Classic Hodgkin Lymphoma All trials of Azacitidine Plus PD-1 therapy
The goal of this phase 2 trial is to test the safety and efficacy of azacitidine when given together with PD-1 therapy in treating patients with relapsed/refractory classic Hodgkin lymphoma.
The investigators will evaluate response rate, progression free survival (PFS), overall survival (OS), and toxicity of azacytidine combined with PD-1 therapy in classic relapsed/refractory Hodgkin lymphoma.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Azacitidine Plus PD-1 therapy | Experimental | Drug: Azacitidine Plus PD-1 therapy | Patients were treated by Azacitidine plus PD-1 therapy |
Sex: All, ages: 18 Years to any
Inclusion Criteria: * Pathologically confirmed Hodgkin Lymphoma according World Health Organization (WHO) classification. * Patient is ≥ 18 years of age at the time of signing the informed consent form (ICF). * Patient must understand and voluntarily sign an ICF prior to any study-specific assessments/procedures being conducted. * Patient is willing and able to adhere to the study visit schedule and other protocol requirements. * Relapsed (after partial or complete response) or refractory AITL after at least one line of systemic therapy (there is no mandatory resting period after the previous treatment as long as the biochemistry and hematology labs meet the inclusion criteria as below). * Meet the following lab criteria: Absolute Neutrophil Count (ANC) ≥ 1,5 x 10\^9/L (≥ 1 x 10\^9/L if bone marrow (BM) involvement by lymphoma); Platelet ≥ 75 x 10\^9/L (≥ 50 x 10\^9/L if BM involvement by lymphoma); Hemoglobin ≥ 8 g/dL. * Anticipated life expectancy at least 3 months. Exclusion Criteria: * Active or uncontrolled infections requiring systemic treatment within 14 days before enrollment. * Any instability of systemic disease, including but not limited to severe cardiac, liver, kidney, or metabolic disease need therapy. * Pregnant or lactating women.
| Facility | City | Country | Status |
|---|---|---|---|
| Navy General Hospital | Beijing, Beijing Municipality | China | Recruiting |