An Open-Label, Dose Escalation, Multi-Center Phase I/II Clinical Trial of EB103 T-Cell Therapy in Adults With Relapsed/Refractory (R/R) B-Cell Non-Hodgkin's Lymphoma (NHL)
Latest Information Update: 26 Feb 2025
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At a glance
- Drugs EB 103 (Primary)
- Indications B-cell lymphoma; Non-Hodgkin's lymphoma
- Focus Adverse reactions; Therapeutic Use
- Acronyms Starlight-1
- 21 Feb 2025 According to Estrella Immunopharma media release, the company announced successful completion of the first dose cohort from this study. Also the Data and Safety Monitoring Board (DSMB) has approved the initiation of the second dose cohort, which will administer 5 million receptor-positive T cells per kilogram of body weight of EB103 CD19-Redirected ARTEMIS T-cell therapy.
- 27 Sep 2024 According to Estrella Immunopharma media release, company announced that the first patient has achieved a complete response (CR) one month after receiving an infusion of EB103 CD19- Redirected ARTEMIS T Cells.
- 14 Aug 2024 According to Estrella Immunopharma, Inc. media release,the Company dosed the first patient in July 2024 from this study.