RecruitingPhase 2NCT06481592

A Study of Lifileucel (Tumor-infiltrating Lymphocytes) in Adults With Advanced Endometrial Cancer.

A Phase 2, Multicenter, Open-label Study of Lifileucel (Tumor-infiltrating Lymphocytes [TIL]) in Participants With Previously Treated Advanced Endometrial Cancer.


Sponsor

Iovance Biotherapeutics, Inc.

Enrollment

60 participants

Start Date

Oct 29, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to investigate the efficacy and safety of the lifileucel regimen in participants with previously treated endometrial cancer.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is testing lifileucel — a treatment made from tumor-infiltrating lymphocytes (TIL), which are immune cells extracted from your own tumor, multiplied in a lab, and reinfused to fight cancer — in adults with advanced endometrial (uterine lining) cancer that has come back or stopped responding to treatment. **You may be eligible if...** - You are 18 or older with advanced endometrial carcinoma (all types except uterine sarcoma) - You have received between 1 and 4 prior lines of treatment, including both platinum-based chemotherapy and an immunotherapy (anti-PD-1/PD-L1) drug - You have measurable disease that can be tracked on scans - Your general health is adequate (ECOG 0–2) - You have tumor tissue available for cell extraction **You may NOT be eligible if...** - You have uterine sarcoma (a different type of uterine cancer) - You have active brain metastases or severe autoimmune disease - You are pregnant or breastfeeding - You have had more than 2 lines of chemotherapy 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BIOLOGICALLifileucel

A tumor sample is resected from each patient and cultured ex vivo to expand the population of tumor infiltrating lymphocytes. After lymphodepleting chemotherapy including cyclophosphamide and fludarabine, participant is infused with lifileucel, followed by IL-2.


Locations(12)

Honor Health

Phoenix, Arizona, United States

University of Southern California

Los Angeles, California, United States

Orlando Health

Orlando, Florida, United States

H. Lee Moffitt Cancer Center and Research Institute, Inc.

Tampa, Florida, United States

Augusta University

Augusta, Georgia, United States

UofL Health - Brown Cancer Center

Louisville, Kentucky, United States

Barbara Ann Karmanos Cancer Hospital

Detroit, Michigan, United States

Roswell Park Cancer Institute

Buffalo, New York, United States

University of Oklahoma

Oklahoma City, Oklahoma, United States

Allegheny Health

Pittsburgh, Pennsylvania, United States

Avera Medical Group Oncology

Sioux Falls, South Dakota, United States

MD Anderson Cancer Center - U of Texas

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06481592


Related Trials