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Tazemetostat and Mosunetuzumab in Untreated Follicular Lymphoma

Phase 2
Recruiting
Conditions
Follicular Lymphoma
Interventions
Registration Number
NCT05994235
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

The goal of this study is to learn about the safety and effectiveness of the combination of tazemetostat pills in combination with mosunetuzumab injections for people with follicular lymphoma who haven't received treatment before. The investigators hypothesize that tazemetostat with mosunetuzumab has the potential to increase the efficacy of the product without compromising the safety.

Tazemetostat is a drug that inhibits EZH2, an enzyme known to drive the development of B-cell lymphomas, and inhibiting it appears to have many effects that slow down lymphoma growth and enhance the immune system's ability to fight it. Tazemetostat is FDA-approved in previously treated follicular lymphoma and currently undergoing study in other lymphomas.

Mosunetuzumab is a bispecific antibody therapy that is a therapeutic strategy that uses the immune system to fight lymphoma, called immunotherapy. Bispecific antibodies have two ends: one attaches to T cells in the immune system and the other attaches to lymphoma cells, helping guide our immune system to attack the cancer. Mosunetuzumab has been studied in follicular lymphoma that has previously been treated, with positive results. Mosunetuzumab is approved by the FDA to be given intravenously (directly into a vein) but is not yet approved by the FDA is not yet approved as an injection under the skin, which is how it is given in this study. They have not yet been studied in combination.

Detailed Description

This is a phase II, open-label study. Fifty patients will be enrolled and treated with standard dosing of SC mosunetuzumab, and with oral tazemetostat by mouth twice daily at standard dosing (800 mg twice daily) beginning at the same time as mosunetuzumab initiation. Response assessments by PET/CT will occur post-mosunetuzumab at Cycle 4, Day 1 (+/- 3 days) and again at the end of treatment. If a participant has a complete response (CR) at Cycle 4 and/or cycle 8, then they will receive a total of 8 cycles of mosunetuzumab. If the patient has a partial response or stable disease at Cycle 4 and Cycle 8, then they will receive a total of 12 cycles of mosunetuzumab. All participants will receive 12 cycles of tazemetostat, unless discontinued from treatment early for disease progression or other protocol-defined reasons. Treatment with steroids, tocilizumab, growth factors, tumor lysis prophylaxis, and antibiotics may be used as per standard of care at our institution. Dose modifications are permitted for toxicity. Correlative studies will be performed prior to and following tazemetostat treatment and peripheral blood collections prior to post-mosunetuzumab treatment, which will give additional descriptive data for use in correlative analyses.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Subcutaneous Mosunetuzumab and Oral TazemetostatTazemetostat Pill50 patients will be enrolled and treated with standard dosing of subcutaneous mosunetuzumab, and with oral tazemetostat by mouth twice daily at standard dosing (800 mg twice daily) beginning at the same time as mosunetuzumab initiation.
Subcutaneous Mosunetuzumab and Oral TazemetostatMosunetuzumab50 patients will be enrolled and treated with standard dosing of subcutaneous mosunetuzumab, and with oral tazemetostat by mouth twice daily at standard dosing (800 mg twice daily) beginning at the same time as mosunetuzumab initiation.
Primary Outcome Measures
NameTimeMethod
Number of participants who achieve a complete response (CR) by completion of therapy, as determined by the Lugano CriteriaEstimated day 336

The proportion of patients who achieve complete response as per the Lugano criteria will be calculated and their 90% confidences will be computed with Clopper-Pearson method via exact binomial distribution.

Secondary Outcome Measures
NameTimeMethod
Number of participants who experience Immune effector cell-associated neurotoxicity syndrome (ICANS)Day 0 to Day 28

ICANS will be assessed per American Society for Transplantation and Cellular Therapy (ASTCT) Consensus Grading

Median Progression-Free Survival (PFS)For a maximum of approximately 10 years

PFS is defined as the duration of time from start of treatment to time of progression or death from any cause. Patients will be followed for a maximum of approximately 10 years from the start of treatment.

Objective Response Rate (ORR) at the time of therapy completion, as defined by Lugano CriteriaEstimated to be day 336

ORR is defined as the proportion of patients who have a partial or complete response to therapy

Number of participants who experience cytokine release syndrome (CRS)Day 0 to Day 28

CRS will be assessed per American Society for Transplantation and Cellular Therapy (ASTCT) Consensus Grading

Median Overall Survival (OS)For a maximum of approximately 10 years

OS is defined as the duration of time from start of treatment to death from any cause. Patients will be followed for a maximum of approximately 10 years from the start of treatment.

Number of participants who achieve a Complete Response (CR) per Lugano's CriteriaFor a maximum of approximately 10 years

Response and progression are evaluated according to the Lugano criteria for lymphoma response.

Median Duration of ResponseFor a maximum of approximately 10 years

The duration of overall response is measured from the time measurement criteria are met for CR or PR (whichever is first recorded) until the first date that recurrent or progressive disease or death due to any cause, whichever occurs first is objectively documented (taking as reference for progressive disease the smallest measurements recorded since the treatment started).

Trial Locations

Locations (1)

Weill Cornell Medicine/NewYork-Presbyterian Hospital

🇺🇸

New York, New York, United States

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