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Clinical Trial Summary

SC291-101 is a Phase 1 study to evaluate SC291 safety and tolerability, anti-tumor activity, cellular kinetics, immunogenicity, and exploratory biomarkers.


Clinical Trial Description

This is an open-label, single arm, Phase 1, first-in-human (FIH) study to evaluate the safety and tolerability of SC291 administered intravenously (IV) following a standard lymphodepleting chemotherapy regimen of cyclophosphamide and fludarabine in subjects with NHL or CLL who have received two or more prior systemic treatments per standard of care (or after autologous stem cell transplant [ASCT] for NHL). This study will be conducted in 2 parts. Phase 1a: dose finding using a 3+3 design in subjects with NHL or CLL. Phase 1b: dose expansion to further evaluate safety and efficacy at the RP2D in subjects with LBCL and CLL. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05878184
Study type Interventional
Source Sana Biotechnology
Contact Ndidi Onwudiwe
Phone 206 791 3731
Email ardent@sana.com
Status Recruiting
Phase Phase 1
Start date May 2, 2023
Completion date December 2027

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