A Study to Evaluate the Efficacy and Safety of Liso-cel Compared to Standard of Care in Adults With Relapsed or Refractory Follicular Lymphoma

NCT06313996 · Status: WITHDRAWN · Phase: PHASE3 · Type: INTERVENTIONAL

Last updated 2026-03-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and safety of Liso-cel compared to standard of care in adults with Relapsed or Refractory Follicular Lymphoma.

Conditions

  • Relapsed or Refractory Follicular Lymphoma

Interventions

DRUG

Cyclophosphamide

Specified dose on specified days

DRUG

Doxorubicin

Specified dose on specified days

DRUG

Vincristine

Specified dose on specified days

DRUG

Rituximab

Specified dose on specified days

DRUG

Prednisone

Specified dose on specified days

DRUG

Bendamustine

Specified dose on specified days

DRUG

Lenalidomide

Specified dose on specified days

DRUG

Fludarabine

Specified dose on specified days

DRUG

Liso-cel

Specified dose on specified days

Sponsors & Collaborators

  • Celgene Corporation

    collaborator INDUSTRY
  • Juno Therapeutics, Inc., a Bristol-Myers Squibb Company

    lead INDUSTRY

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-29
Primary Completion
2031-10-16
Completion
2031-10-16
FDA Drug
Yes

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06313996 on ClinicalTrials.gov