RecruitingPhase 2NCT06743945

POLA-R-CHP in the First-line Treatment of Transformed DLBCL

A Prospective, Multicenter, Phase II Study of POLA-R-CHP in the First-line Treatment of Transformed DLBCL


Sponsor

Fudan University

Enrollment

20 participants

Start Date

Feb 17, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to evaluate efficacy and safety of POLA-R-CHP in the treatment of patients with transformed DLBCL.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study tests a first-line chemotherapy combination called POLA-R-CHP (which includes a targeted antibody-drug conjugate called polatuzumab vedotin along with rituximab and chemotherapy) for people with transformed diffuse large B-cell lymphoma (DLBCL) — a type of aggressive lymphoma that has changed from a slower-growing lymphoma. **You may be eligible if...** - You are between 18 and 80 years old - You have been confirmed by biopsy to have transformed DLBCL - You are in good physical condition (ECOG 0–2) - Your blood counts, liver, kidney, and heart function are adequate **You may NOT be eligible if...** - You are allergic to monoclonal antibodies - You have had a prior organ transplant - You have received cytotoxic chemotherapy or anti-CD20 antibody therapy in the past 5 years - You have significant heart or lung disease - You have active or uncontrolled serious infection - You have active hepatitis B, active hepatitis C, HIV, or syphilis - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

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

DRUGPOLA-R-CHP

Pola-R-CHP is a combination of rituximab, cyclophosphamide, doxorubicin, prednisone, and polatuzumab vedotin


Locations(1)

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

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NCT06743945


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