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Clinical Trial Summary

This is an open-label, dose escalation, multi-center, Phase I/II clinical trial to assess the safety of an autologous T-cell therapy (EB103) and to determine the Recommended Phase II Dose (RP2D) in adult subjects (≥ 18 years of age) who have relapsed/refractory (R/R) B-cell NHL. The study will include a dose escalation phase followed by an expansion phase.


Clinical Trial Description

This is an open-label, dose escalation, multi-center, Phase I/II clinical trial to assess the safety of EB103 and determine the RP2D in adult subjects (≥ 18 years of age) who have R/R B-cell NHL. The study will include a dose escalation phase followed by an expansion phase. A traditional dose escalation model (3+3 design) will be used to determine the RP2D, and once determined, the expansion phase will commence. Additional subjects will be enrolled in the expansion phase to further confirm the safety profile of EB103 at the RP2D and evaluate the preliminary efficacy of EB103. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06343311
Study type Interventional
Source Estrella Immunopharma, Inc.
Contact Teresa Klask, MBA
Phone 925-949-9314
Email teresa.klask@eurekainc.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date June 15, 2024
Completion date December 31, 2027

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