RecruitingPhase 1NCT07332507

Testing the Effect of Teclistamab on Recurrent Plasmablastic Lymphoma

Phase 1b Study of Teclistamab in Relapsed/Refractory Plasmablastic Lymphoma


Sponsor

National Cancer Institute (NCI)

Enrollment

30 participants

Start Date

Mar 26, 2027

Study Type

INTERVENTIONAL

Conditions

Summary

This phase Ib trial tests the safety, side effects, and best dose of teclistamab in treating patients with plasmablastic lymphoma that has come back after a period of improvement (recurrent) or that has not responded to previous treatment (refractory). Teclistamab is a bispecific antibody that can bind to two different antigens at the same time. Teclistamab binds to B-cell maturation antigen (BCMA), a protein found on some B-cells and myeloma cells, and CD3 on T-cells (a type of white blood cell) and may interfere with the ability of cancer cells to grow and spread. Giving teclistamab may be safe and tolerable in treating patients with recurrent or refractory plasmablastic lymphoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Biospecimen Collection, a procedure called Computed Tomography, and others for people with recurrent plasmablastic lymphoma and refractory plasmablastic lymphoma. The study is currently recruiting participants at 1 location. 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

PROCEDUREBiospecimen Collection

Undergo buccal swab and blood sample collection

PROCEDUREComputed Tomography

Undergo PET/CT

PROCEDUREPositron Emission Tomography

Undergo PET/CT

DRUGTeclistamab

Given SC


Locations(1)

City of Hope Comprehensive Cancer Center LAO

Duarte, California, United States

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NCT07332507


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