A Phase III Trial Comparing Tisagenlecleucel to Standard of Care (SoC) in Adult Participants With r/r Follicular Lymphoma

Description

This trial will compare tisagenlecleucel to standard of care in adult participants with relapsed or refractory (r/r) follicular lymphoma.

Conditions

Follicular Lymphoma (FL)

Study Overview

Study Details

Study overview

This trial will compare tisagenlecleucel to standard of care in adult participants with relapsed or refractory (r/r) follicular lymphoma.

A Randomized, Open-label, Multi-center Phase III Trial Comparing Tisagenlecleucel to Standard of Care in Adult Participants With Relapsed or Refractory Follicular Lymphoma (FL)

A Phase III Trial Comparing Tisagenlecleucel to Standard of Care (SoC) in Adult Participants With r/r Follicular Lymphoma

Condition
Follicular Lymphoma (FL)
Intervention / Treatment

-

Contacts and Locations

Cincinnati

TRIHEALTH Good Samarithan Hospital, Cincinnati, Ohio, United States, 45220

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Age ≥ 18 years at the date of signing the informed consent form.
  • 2. Follicular lymphoma grade 1, 2, or 3A confirmed histologically after latest relapse (local assessment).
  • 3. Relapsed or refractory disease after a second or later line of systemic therapy including an anti-CD20 antibody and an alkylating agent.
  • 4. Disease that is both active on Positron emission tomography (PET) scan (defined as a score of 4 or 5 on the Deauville 5-point scale) and measurable on Computed tomography (CT) scan.
  • 5. ECOG performance status of 0, 1 or 2 at screening.
  • 6. Adequate hematologic, renal, hepatic and pulmonary organ function at screening.
  • 7. Must meet the institutional criteria to undergo leukapheresis (unless historical leukapheresis is available).
  • 8. Must be eligible for treatment with the selected standard of care regimen.
  • 1. Follicular lymphoma grade 3B or evidence of histologic transformation.
  • 2. Prior treatment with anti-CD19 therapy, gene therapy, or adoptive T-cell therapy.
  • 3. Active CNS involvement by malignancy.
  • 4. Clinically significant active infection, presence of Human immunodeficiency virus (HIV) antibody or active hepatitis B or C.
  • 5. Active neurological autoimmune or inflammatory disorders (e.g., Guillain-Barré syndrome).
  • 6. Investigational medicinal product within the last 30 days or five half-lives (whichever is longer) prior to randomization.
  • 7. Clinically significant cardiovascular conditions such as acute coronary syndrome, significant cardiac arrhythmias, heart failure or decreased LVEF.

Ages Eligible for Study

18 Years to 100 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Novartis Pharmaceuticals,

Novartis Pharmaceuticals, STUDY_DIRECTOR, Novartis Pharmaceuticals

Study Record Dates

2031-01-18