Phase 2 Study Evaluating Autologous CD30.CAR-T Cells in Adult and Pediatric Patients With Relapsed/Refractory HL

2020-02-19 18:28:41 | BioPortfolio


This is a Phase 2 study to evaluate the safety and efficacy of autologous CD30.CAR-T in subjects with relapsed or refractory CD30+ classical Hodgkin Lymphoma.


Subjects who meet eligibility criteria will have blood drawn to manufacture the CD30.CAR-T cells in a lab. CD30.CAR-T cells will be infused after the completion of lymphodepleting chemotherapy with fludarabine and cyclophosphamide.

Subjects will be monitored for safety and efficacy throughout the study. Subjects will be followed for survival, withdrawal of consent or study closure, whichever occurs first.

Health Related Quality of Life assessments will be collected for pediatric and adult patients during the study.

Study Design


Hodgkin Lymphoma, Adult




Not yet recruiting


Tessa Therapeutics

Results (where available)

View Results


Published on BioPortfolio: 2020-02-19T18:28:41-0500

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Medical and Biotech [MESH] Definitions

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