Brentuximab Vedotin and Pembrolizumab in Treating Patients With Recurrent Peripheral T-Cell Lymphoma
NCT04795869 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2023-10-10
Summary
This phase II clinical trial studies how well giving brentuximab vedotin together with pembrolizumab in treating patients with peripheral T-cell lymphoma (PTCL) that has come back (recurrent). Monoclonal antibody-drug conjugates, such as brentuximab vedotin, can block cancer growth in different ways by targeting certain cells. Pembrolizumab is an antibody-drug that stimulates body's natural antitumor immune responses. Giving brentuximab vedotin together with pembrolizumab may work better than brentuximab vedotin alone in treating patients with recurrent peripheral T-cell lymphoma.
Conditions
- Recurrent Angioimmunoblastic T-Cell Lymphoma
- Recurrent Enteropathy-Associated T-Cell Lymphoma
- Recurrent Follicular T-Cell Lymphoma
- Recurrent Hepatosplenic T-Cell Lymphoma
- Recurrent Nodal Peripheral T-Cell Lymphoma With TFH Phenotype
- Recurrent Peripheral T-Cell Lymphoma, Not Otherwise Specified
- Recurrent Subcutaneous Panniculitis-Like T-Cell Lymphoma
- Refractory Angioimmunoblastic T-Cell Lymphoma
- Refractory Enteropathy-Associated T-Cell Lymphoma
- Refractory Follicular T-Cell Lymphoma
- Refractory Hepatosplenic T-Cell Lymphoma
- Refractory Nodal Peripheral T-Cell Lymphoma With TFH Phenotype
- Refractory Peripheral T-Cell Lymphoma, Not Otherwise Specified
- Refractory Subcutaneous Panniculitis-Like T-Cell Lymphoma
Interventions
- DRUG
-
Brentuximab Vedotin
Given IV
- BIOLOGICAL
-
Given IV
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH - collaborator INDUSTRY
-
Seagen Inc.
collaborator INDUSTRY - lead OTHER
Principal Investigators
-
Jonathan Moreira, MD · Northwestern University
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-03-01
- Primary Completion
- 2026-03-15
- Completion
- 2029-03-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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