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Study details
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Clinical Trial of CD40L-Augmented TIL for Advanced Melanoma

H. Lee Moffitt Cancer Center and Research Institute
NCT IDNCT06961357ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

36

Study length

about 4.4 years

Ages

18+

Locations

1 site in FL

About this study

This trial is testing a single dose of CD40L-augmented TIL in patients with advanced melanoma. Patients will undergo lymphodepletion followed by the TIL product and standard of care interleukin-2.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Cyclophosphamide
  • 2.Take Fludarabine
  • 3.Take Interleukin-2
  • +1 more
PhasePhase 1/Phase 2
DrugCyclophosphamide
Routeinfusion
Primary goalPhase I: Treatment Emergent Adverse Events (TEAE)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), fludarabine, immunotherapy (Cytokine; stimulates T-cells to proliferate)

Drug routes

infusion

Endpoints

Primary: Phase I: Treatment Emergent Adverse Events (TEAE), Phase II: Objective Response Rate

Secondary: Duration of response, Overall survival, Progression Free Survival (PFS)

Body systems

Oncology