Lymphoma

12 protocols meet the specified criteria.
  • A051901

    Phase I Trial of Methotrexate, Rituximab, Lenalidomide, and Nivolumab (NIVO-MR2) Induction followed by Lenalidomide and Nivolumab Maintenance in Primary CNS Lymphoma
  • A151804

    Establishment of a National Biorepository to Advance Studies of Immune-Related Adverse Events
  • A211901

    Reaching Rural Cancer Survivors Who Smoke Using Test-Based Cessation Interventions
  • CCTL019B2003I

    Managed Access Program (MAP) to provide access to CTL019, for acute lymphoblastic leukemia (ALL) in diffuse large b-cell lymphoma (DLBCL) patients with out of specification leukapheresis product and/or manufactured tisagenlecleucel out of specification for commercial release
  • EAY191

    Molecular Analysis for Combination Therapy Choice (ComboMATCH)
  • EZH-302

    SYMPHONY-1: A Phase 1B/3 Double-blind, Randomized, Active-Controlled, 3-Stage, Biomarker Adaptive Study of Tazemetostat/EPZ-6438 or Placebo in Combination with Lenalidomide plus Rituximab (R^2) in Subjects with Relapsed/Refractory Follicular Lymphoma
  • GO43878

    A Phase III, Open-Label, Multicenter, Randomized Study Evaluating Glofitamab as a Single Agent Versus Investigator's Choice in Patients with Relapsed/Refractory Mantle Cell Lymphoma
  • GO44145

    SKYGLO: A Phase III, Multicenter, Randomized, Open-Label Study Comparing the Safety and Efficacy of Glofitimab (RO7082859) in Combination with Polatuzumab Vedotin plus Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone (Pola-R-CHP) versus Pola-R-CHP in Previously Untreated Patients with Large B-Cell Lymphoma
  • INCA-34176-357

    A Phase 3, Randomized, Double-blind, Placebo-Controlled Study of Axatilimab and Corticosteroids as Initial Treatment for Chronic Graft-Versus-Host Disease
  • JCAR017-EAP-001

    Expanded Access Protocol (EAP) for Subjects Receiving Lisocabtagene Maraleucel that is Nonconforming for Commercial Release
  • KT-US-472-0141

    Expanded access to commercially out-of-specification brexucabtagene autoleucel for the treatment of adult patients diagnosed with an FDA approved labeled indication
  • WVU010922

    Prospective Evaluation of Xerava (Eravacycline) Prophylaxis in Hematological Malignancy Patients with Prolonged Neutropenia