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ACTIVE NOT RECRUITING
NCT05145062

Long - Term Follow Up of Sickle Cell Disease and Beta-thalassemia Subjects Previously Exposed to BIVV003 or ST-400.

Sponsor: Sangamo Therapeutics

View on ClinicalTrials.gov

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

Official title: An Observational Long-term Safety and Efficacy Follow-up Study After Ex-vivo Gene Therapy With BIVV003 in Participants With Severe Sickle Cell Disease (SCD) or With ST-400 in Participants With Transfusion-dependent Beta-thalassemia (TDT) With Autologous Hematopoietic Stem Cell Transplant

Key Details

Gender

All

Age Range

18 Years - 45 Years

Study Type

OBSERVATIONAL

Enrollment

8

Start Date

2021-12-21

Completion Date

2038-07-14

Last Updated

2025-11-12

Healthy Volunteers

No

Interventions

DRUG

BIVV003

Solution for intravenous administration

DRUG

ST-400

Solution for intravenous administration

Locations (7)

UCSF Benioff Children's Hospital

Oakland, California, United States

University of California Davis Health System

Sacramento, California, United States

Children's Healthcare of Atlanta

Atlanta, Georgia, United States

Boston Children's Hospital

Boston, Massachusetts, United States

Karmanos Cancer Institute

Detroit, Michigan, United States

Henry Ford Health System

Detroit, Michigan, United States

University of Minnesota

Minneapolis, Minnesota, United States