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Spots Global Cancer Trial Database for Effect of Blinatumomab on Minimal Residual Disease (MRD) in Diffuse Large B-Cell Lymphoma (DLBCL) Subjects Post Autologous Hematopoietic Stem Cell Transplantation (aHSCT)

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Trial Identification

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

Interventions

Blinatumomab

Study Description

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.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: MD

Affiliation: Amgen

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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