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Brief Title: Effect of Blinatumomab on Minimal Residual Disease (MRD) in Diffuse Large B-Cell Lymphoma (DLBCL) Subjects Post Autologous Hematopoietic Stem Cell Transplantation (aHSCT)
Official Title: A Phase 2 Open-Label Study to Determine the Effect of Blinatumomab on Minimal Residual Disease in Subjects With High-risk Diffuse Large B-cell Lymphoma Post-autologous Hematopoietic Stem-cell Transplantation.
Study ID: NCT03298412
Brief Summary: The study will estimate the MRD-negative response rate after treatment with blinatumomab in subjects with high-risk DLBCL who are MRD-positive following aHSCT. The clinical hypothesis is that the MRD-negative response rate will be greater than 10%. Achieving an MRD-negative response rate of 30% would be of scientific and clinical interest.
Detailed Description: This is a phase 2, multicenter, open-label, single arm estimation study in adult subjects with high-risk DLBCL in complete remission. The study will consist of up to a 28-day screening period, a run-in period of up to 24 months, a 12-week treatment period (8 weeks of blinatumomab treatment followed by a 4-week treatment free period), a 30-day safety follow-up visit after the last dose of blinatumomab, and a long-term follow-up period that begins after the safety follow-up visit is completed until 1 year from the first dose of blinatumomab. The study will enroll approximately 90 subjects in the screening period with biopsy proven, high-risk DLBCL that are positron emission tomography-computer tomography (PET-CT) negative 90 days (± 30 days) post aHSCT. During the run-in period subjects will be followed by clinic visits at regular interval for up to 24 months for monitoring of MRD status in plasma by a next generation sequencing (NGS)-based assay. It is estimated 30 subjects will be either MRD-positive at screening or become MRD-positive during the 24-month run-in period. The number of subjects enrolled may be altered in order to ensure that approximately 30 subjects are assigned to treatment with blinatumomab. Enrollment may be stopped, once approximately 30 subjects have been assigned to treatment with blinatumomab.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, Atlanta, Georgia, United States
Research Site, Maywood, Illinois, United States
Research Site, Cleveland, Ohio, United States
Research Site, Dallas, Texas, United States
Research Site, St Leonards, New South Wales, Australia
Research Site, Westmead, New South Wales, Australia
Research Site, Clayton, Victoria, Australia
Research Site, Geelong, Victoria, Australia
Research Site, Charleroi, , Belgium
Research Site, Leuven, , Belgium
Research Site, Liege, , Belgium
Research Site, Créteil Cedex, , France
Research Site, Lille, , France
Research Site, Marseille, , France
Research Site, Montpellier cedex 5, , France
Research Site, Paris Cedex 10, , France
Research Site, Pessac Cedex, , France
Research Site, Pierre Benite Cedex, , France
Research Site, Rouen, , France
Research Site, Athens, , Greece
Research Site, Athens, , Greece
Research Site, Thessaloniki, , Greece
Research Site, Bergamo, , Italy
Research Site, Brescia, , Italy
Research Site, Firenze, , Italy
Research Site, Milano, , Italy
Research Site, Palermo, , Italy
Research Site, Torino, , Italy
Research Site, Bellinzona, , Switzerland
Research Site, Bern, , Switzerland
Research Site, Lausanne, , Switzerland
Research Site, Zurich, , Switzerland
Name: MD
Affiliation: Amgen
Role: STUDY_DIRECTOR