RecruitingPhase 2NCT05786040

Tafasitamab and Rituximab for Front-Line Treatment of Post-Transplant Lymphoproliferative Disorder

Phase II Study to Assess the Efficacy of Combined Tafasitamab and Rituximab in Front-Line Treatment of Post-Transplant Lymphoproliferative Disorder


Sponsor

Timothy Voorhees

Enrollment

28 participants

Start Date

Mar 23, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial tests how well tafasitamab and rituximab work for front-line treatment of patients with post-transplant lymphoproliferative disorder. Post-transplant lymphoproliferative disorder (PTLD) is the name for types of lymphoma that sometimes develop in people who have had a transplant. It can affect people who are taking medicines to suppress their immune system. Tafasitamab injection is in a class of medications called monoclonal antibodies. It works by helping the body to slow or stop the growth of cancer cells. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Giving the combination of tafasitamab and rituximab may work better in treating patients with post-transplant lymphoproliferative disorder.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Biopsy, a procedure called Biospecimen Collection, and others for people with monomorphic b-cell post-transplant lymphoproliferative disorder and polymorphic post-transplant lymphoproliferative disorder. The study is currently recruiting participants at 4 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiopsy

Undergo biopsy

PROCEDUREBiospecimen Collection

Undergo collection of blood samples

PROCEDUREComputed Tomography

Undergo CT

PROCEDUREPositron Emission Tomography

Undergo PET

BIOLOGICALRituximab

Given IV or SC

BIOLOGICALTafasitamab

Given IV


Locations(4)

Rutgers Cancer Institute of New Jersey

New Brunswick, New Jersey, United States

University of North Carolina-Hillsborough Campus

Hillsborough, North Carolina, United States

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

Huntsman Cancer Institute

Salt Lake City, Utah, United States

View Full Details on ClinicalTrials.gov

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NCT05786040