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Study of Lifileucel (LN-144), Autologous Tumor Infiltrating Lymphocytes, in the Treatment of Patients With Metastatic Melanoma

Phase 2
Completed
Conditions
Metastatic Melanoma
Interventions
Registration Number
NCT02360579
Lead Sponsor
Iovance Biotherapeutics, Inc.
Brief Summary

Prospective, interventional multicenter study evaluating adoptive cell therapy (ACT) via infusion of LN-144 (autologous TIL) followed by interleukin 2 (IL-2) after a nonmyeloablative lymphodepletion (NMA LD) preconditioning regimen.

Detailed Description

Lifileucel is an autologous adoptive cell transfer therapy that utilizes a TIL manufacturing process, as originally developed by the NCI, for the treatment of patients with metastatic melanoma. The adoptive cell transfer therapy used in this study involves patients receiving a lymphocyte depleting preconditioning regimen, prior to infusion of autologous TIL, followed by the administration of a regimen of IL-2.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
178
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cohort 4LifileucelCryopreserved lifileucel (LN-144) (Gen 2 infusion product)
Cohort 1LifileucelLifileucel (LN-144) without cryopreservation (Gen 1 infusion product) (Closed)
Cohort 2LifileucelCryopreserved lifileucel (LN-144) (Gen 2 infusion product) (Closed)
Cohort 3LifileucelRetreatment cohort: patients from Cohort 1, Cohort 2 or Cohort 4 may rescreen for a second TIL regimen therapy if they meet all Inclusion and Exclusion Criteria (except exclusion criterion b).
Primary Outcome Measures
NameTimeMethod
Disease Assessment for Objective Response RateEvery 6 weeks for 6 months, then every 3 months for a maximum of 60 months

Evaluate the efficacy of LN-144 in patients with unresectable or metastatic melanoma using the objective response rate (ORR), as assessed by the Blinded Independent Review Committee (BIRC) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1

Secondary Outcome Measures
NameTimeMethod
Overall SurvivalUntil death or up to 60 months

Evaluate overall survival (OS) and objective response rate (ORR) by the investigator

Disease Assessment for Duration of ResponseEvery 6 weeks for 6 months, then every 3 months for a maximum of 60 months

Evaluate the efficacy endpoints of duration of response (DOR) by the BIRC and by the investigator per RECIST v1.1

Adverse EventsMaximum 60 months

Incidence rate of treatment-emergent adverse events (AEs) and serious AEs by severity and relationship to Lifileucel (LN-144).

Disease Assessment for Disease Control RateEvery 6 weeks for 6 months, then every 3 months for a maximum of 60 months

Evaluate the efficacy endpoints of disease control rate (DCR) as assessed by the BIRC and by the investigator per RECIST v1.1

Disease Assessment for Progression-Free SurvivalEvery 6 weeks for 6 months, then every 3 months for a maximum of 60 months

Evaluate the efficacy endpoints of progression-free survival (PFS) as assessed by the BIRC and by the investigator per RECIST v1.1

Trial Locations

Locations (57)

University of California San Diego Moores Cancer Center

🇺🇸

La Jolla, California, United States

The Angeles Clinic and Research Institute

🇺🇸

Los Angeles, California, United States

University of California Los Angeles - David Geffen School of Medicine - Westwood Rheumatology

🇺🇸

Los Angeles, California, United States

California Pacific Medical Center

🇺🇸

San Francisco, California, United States

University of Colorado Cancer Center

🇺🇸

Aurora, Colorado, United States

Yale Cancer Center

🇺🇸

New Haven, Connecticut, United States

Mount Sinai Comprehensive Cancer Center

🇺🇸

Miami Beach, Florida, United States

University of Miami

🇺🇸

Miami, Florida, United States

University of Florida Health Cancer Center

🇺🇸

Orlando, Florida, United States

University of South Florida H. Lee Moffitt Cancer Center and Research Institute

🇺🇸

Tampa, Florida, United States

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University of California San Diego Moores Cancer Center
🇺🇸La Jolla, California, United States

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