Study Summary
The study will evaluate safety and efficacy of a combination of 4th generation chimeric antigen receptor gene-modified T cells targeting CD19 (4SCAR19) and CD20 (4SCAR20), CD22 (4SCAR22), CD30 (4SCAR30), CD38 (4SCAR38), CD70 (4SCAR70) or CD123 (4SCAR123) for patients with B cell malignancies. Clinical response and development of a standardized lentiviral vector and cell production protocol will be investigated. This is a phase I/II trial enrolling patients from multiple clinical centers.
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4SCAR19 and 4SCAR22BIOLOGICAL
4SCAR19 and 4SCAR22
4SCAR19 and 4SCAR38BIOLOGICAL
4SCAR19 and 4SCAR38
4SCAR19 and 4SCAR20BIOLOGICAL
4SCAR19 and 4SCAR20
4SCAR19 and 4SCAR123BIOLOGICAL
4SCAR19 and 4SCAR123
4SCAR19 and 4SCAR70BIOLOGICAL
4SCAR19 and 4SCAR70
4SCAR19 and 4SCAR30BIOLOGICAL
4SCAR19 and 4SCAR30
Study Locations
| Facility | City | State | Country |
|---|---|---|---|
| Zhujiang Hospital of Southern Medical University | Guangzhou | Guangdong | China |
| Zhujiang Hospital of Southern Medical University | Guangzhou | Guangdong | China |
| Shenzhen Geno-immune Medical Institute | Shenzhen | Guangdong | China |
| Yunnan Cancer Hospital & The Third Affiliated Hospital of Kunming Medical University & Yunnan Cancer Center | Kunming | Yunnan | China |