A Study Evaluating Gene Therapy With BB305 Lentiviral Vector in Sickle Cell Disease

PHASE3Active, not recruitingINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

February 14, 2020

Primary Completion Date

May 31, 2027

Study Completion Date

November 30, 2027

Conditions
Sickle Cell Disease
Interventions
GENETIC

bb1111

Drug Product is administered by IV infusion following myeloablative conditioning with busulfan.

Trial Locations (9)

10467

Montefiore Medical Center, The Bronx

20010

Children's National Hospital, Washington D.C.

23219

Virginia Commonwealth University (VCU), Richmond

27705

Duke University, Durham

35233

University of Alabama, Birmingham

55455

University of Minnesota, Minneapolis

77030

Baylor College of Medicine/Texas Children's Hospital, Houston

02111

Tufts Medical Center, Boston

07601

Hackensack University Medical Center, Hackensack

Sponsors
All Listed Sponsors
lead

Genetix Biotherapeutics Inc.

INDUSTRY

NCT04293185 - A Study Evaluating Gene Therapy With BB305 Lentiviral Vector in Sickle Cell Disease | Biotech Hunter | Biotech Hunter