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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Cyclophosphamide
  • 2.Take Fludarabine
  • 3.Take Interleukin-2
  • +1 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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