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Study details
Enrolling now

Gene Modified Immune Cells After Conditioning Regimen for Melanoma or Solid Tumors

Anusha Kalbasi
NCT IDNCT04119024ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

18

Study length

about 1.1 years

Ages

18–75

Locations

3 sites in CA

What this study is about

This trial is testing a new treatment using gene-modified immune cells (IL13Ralpha2 CAR T cells) after chemotherapy. The goal is to find the safest dose and see how long these modified cells stay in your body while attacking cancer cells.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Fludeoxyglucose F-18
  • 2.Receive IL13Ralpha2-specific Hinge-optimized 4-1BB-co-stimulatory CAR/Truncated CD19-expressing Autologous TN/MEM Cells
  • 3.Take Cyclophosphamide
  • +3 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 / IVInjection / 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), Antineoplastic Agent [TC] (Nucleic Acid Synthesis Inhibitors), fludeoxyglucose (18F)

Drug routes

infusion, injection (Injection)

Endpoints

Primary: Dose-limiting toxicity, Incidence of adverse events

Secondary: Complete response (CR), Duration of overall response, Objective response rate, Overall survival, Partial response (PR), Progression-free survival, Time to disease progression

Procedures

biopsy, diagnostic, imaging

Body systems

Oncology, Respiratory