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Clinical Trial Summary

Primary Objectives: Long-term safety of BIVV003 in participants with severe sickle cell disease (SCD) and ST- 400 in participants with transfusion-dependent beta-thalassemia (TDT) Secondary Objectives: - Long-term efficacy of the biological treatment effect of BIVV003 in SCD - Long-term efficacy of the clinical treatment effect of BIVV003 on SCD-related clinical events - Long-term efficacy of the biological treatment effect of ST-400 in TDT - Long-term efficacy of the clinical treatment effect of ST-400 in TDT


Clinical Trial Description

The total study duration is up to 15 years of follow-up post BIVV003 and/or ST-400 infusion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05145062
Study type Observational
Source Sangamo Therapeutics
Contact
Status Enrolling by invitation
Phase
Start date December 21, 2021
Completion date July 14, 2038