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Study of Autologous Tumor Infiltrating Lymphocytes in Patients With Solid Tumors

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NCT03645928

Sponsored by Iovance Biotherapeutics, Inc. (industry) · IOVA — their whole pipeline →.

Phase
Phase 2
Status
Terminated
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
225actual
Sites
34
Countries
Canada, Germany, Greece +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

After reviewing the available safety and efficacy data to date, Iovance concluded that the study reached the required number of events for evaluation of study endpoints.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2019-05-07actualWhen the study began enrolling
Primary completion2026-02-20actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-02-20actualThe whole study's end, after follow-up
First posted2018-08-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-15actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Metastatic Melanoma
  • Squamous Cell Carcinoma of the Head and Neck
  • Non-small Cell Lung Cancer

Interventions

  • Biological: Lifileucel — also filed as LN-144, TIL, autologous tumor-infiltrating lymphocytes
  • Biological: LN-145 — also filed as TIL, autologous tumor infiltrating lymphocytes
  • Drug: Pembrolizumab — also filed as Keytruda
  • Biological: LN-145-S1 — also filed as TIL, autologous tumor-infiltrating lymphocytes, PD-1-selected TIL
  • Drug: Ipilimumab — also filed as Yervoy
  • Drug: Nivolumab — also filed as Opdivo
  • Drug: Nivolumab-relatlimab — also filed as Opdualag
  • Drug: Cisplatin
  • Drug: Carboplatin
  • Drug: Paclitaxel
  • Drug: Nab paclitaxel
  • Drug: Pemetrexed

Primary outcomes

what the primary-completion date above is the date OF
Objective Response Rate
measured Up to 60 months
Safety Profile Measured by Grade ≥3 TEAEs
measured Up to 60 months
Percentage of patients for whom lifileucel is successfully manufactured and meets release specification
measured Up to 60 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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