RecruitingPhase 1NCT05618366

Tazemetostat and Venetoclax in Relapsed/Refractory Non-Hodgkin Lymphoma

Phase I Trial of Tazemetostat in Combination With Venetoclax in Patients With Relapsed/Refractory Non-Hodgkin Lymphoma


Sponsor

Weill Medical College of Cornell University

Enrollment

38 participants

Start Date

Jun 7, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to learn about how a combination of tazemetostat and venetoclax in people with relapsed/refractory Non-Hodgkin Lymphoma (R/R NHL). The main questions that this trial aims to answer are what is the best dose of venetoclax to give with tazemetostat to people with R/R NHL; what types of side effects do people with R/R NHL get when taking venetoclax with tazemetostat; and what effects does this combination have on R/R NHL. Participants will need to take pills by mouth every day and regularly come to the clinic for blood work and imagining to monitor side effects and cancer progression. Participants may receive study drugs for up to 24 months.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing the combination of two cancer drugs — tazemetostat (an epigenetic targeted drug) and venetoclax (which causes cancer cells to self-destruct) — in people with certain types of non-Hodgkin lymphoma that have returned or stopped responding to prior treatments. **You may be eligible if...** - You are 18 or older with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma (FL) - You have received at least two prior lines of therapy (for DLBCL) or at least two prior treatments (for FL) - You have at least one measurable tumor site of 1.5 cm or larger - Your blood counts and organ function meet required levels - You need treatment as determined by your doctor **You may NOT be eligible if...** - You have not tried prior standard treatments - Your blood counts, liver, or kidney function are too low - You have active serious infections or uncontrolled health conditions - 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

DRUGVenetoclax

Participants will receive oral venetoclax taken once per day. The dose will be between 200 and 800 mg daily, with the exact dose determined by the protocol.

DRUGTazemetostat

Tazemetostat 800mg taken orally, twice daily.


Locations(1)

Weill Cornell Medicine/NewYork-Presberteryian Hospital

New York, New York, United States

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NCT05618366


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