ADI-001: No study drug is administered in this study. Patients who have received Adicet allogeneic γδ CAR T cell therapy will be evaluated in this trial for long-term safety and efficacy
The purpose of this study is to assess long-term side effects from subjects who receive an Adicet Bio γδ CAR T cell product. Subjects will join this study once they complete the parent interventional study. No additional study drug will be given, but subjects can receive other therapies for their cancer while they are being followed for long term safety in this study. For a period of 15 years from the first administration of Adicet Bio allogeneic γδ CAR T cell product, subjects will be assessed for long-term safety and survival through collection of data that include safety, efficacy, pharmacokinetics and immunogenicity.
| Facility | City | Region | Status |
|---|---|---|---|
| Blood and Marrow Transplant Program | Palo Alto | California | |
| Norton Cancer Institute | Louisville | Kentucky | |
| Baylor Scott & White Research Institute | Dallas | Texas | |
| MD Anderson Caner Center | Houston | Texas | |
| Medical College of Wisconsin | Milwaukee | Wisconsin |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04911478 on ClinicalTrials.gov ↗ ← All trials in the USA