AFPᶜ³³²T in Advanced HCC
Completed · Phase 1
Conditions studied: Hepatocellular Cancer, AFP Expressing Tumors
In brief
This first time in human study is intended for men and women between 18 and 75 years of age who have advanced liver cancer which has grown or returned after being treated or another AFP expressing tumor. Those who did not tolerate or refused other therapies may also participate. The purpose of this study is to test the safety of genetically changed T cells that target alpha-fetoprotein (AFP) and find out what effects, if any, they have in subjects with liver cancer or other AFP expressing tumor types. This study is for subjects who have a blood test positive for appropriate HLA-A\*02 P Group and have adequate AFP protein in blood or tumor, and whose noncancerous liver tissue has very little AFP protein (Liver only). The study will take the subject's T cells, which are a natural type of immune cell in the blood, and send them to a laboratory to be modified. The changed T cells used in this study will be the subject's own T cells that have been genetically changed with the aim of attacking and destroying cancer cells. The manufacturing of T cells takes about 1 month to complete. The T cells will be given back to the subject through an intravenous infusion after 3 days of chemotherapy. The study will evaluate three different cell dose levels in order to find out the target cell dose. Once the target cell dose is determined, additional subjects will be enrolled to further test the safety and effects at this cell dose. Subjects will be hospitalized for at least 1 week after receiving their T cells back and then seen frequently by the Study Physician for the next 6 months. After that, subjects will be seen every three months. If subjects have disease progression or withdraw from the study, they will then be entered into a long-term follow up for safety monitoring. In long-term follow up, subjects will be seen every 6 months by their Study Physician for the first 5 years after the T cell infusion and annually for the next 10 years.
Key facts
- Study ID
- NCT03132792
- Run by
- Adaptimmune
- People needed
- 39
- Starts
- 2017-05-08
- Expected to finish
- 2025-11-19
- Last updated by the study team
- 2026-06-17
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Mayo Clinic Arizona — Phoenix, Arizona, United States
- USC/Norris Comprehensive Cancer Center — Los Angeles, California, United States
- UCLA — Los Angeles, California, United States
- University of Miami — Miami, Florida, United States
- Winship Cancer Institute - Emory University — Atlanta, Georgia, United States
- University of Maryland, Greenebaum Cancer Center — Baltimore, Maryland, United States
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Mayo Clinic Clinical Trial Referral Office — Rochester, Minnesota, United States
- Washington University - School of Medicine — St Louis, Missouri, United States
- MD Anderson Cancer Center — Houston, Texas, United States
- Fred Hutchinson Cancer Research Centre — Seattle, Washington, United States
- SCCA Immunotherapy Trials Intake — Seattle, Washington, United States
- Paoli Calmettes Institute — Marseille, France
- Centre Eugène Marquis — Rennes, France
- Institute Gustave Roussy — Villejuif, France
- University Hospital of Barcelona — Barcelona, Spain
- University Hospital of Navarra — Pamplona, Spain
- Beatson West of Scotland Cancer Centre — Glasgow, United Kingdom
- Guy's Hospital — London, United Kingdom
- NIHR UCLH Clinical Research — London, United Kingdom
- The Christie NHS Foundation Trust — Manchester, United Kingdom
Full record on ClinicalTrials.gov
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