Anthony J. Aldave, MD

California's Stem Cell Agency Logo

California Institute for Regenerative Medicine

Role:               Principal Investigator
Duration:         08/01/23-02/28/26
Description:     AAV gene therapy for treating congenital hereditary endothelial dystrophy associated with biallelic SLC4A11 mutations

 

Foundation for the National Institutes of Health

Foundation for the National Institutes of Health
Accelerating Medicines Partnership® (AMP®) Bespoke Gene Therapy Consortium (BGTC)

Role:               Principal Investigator
Duration:         05/28/23-05/27/28
Description:     Phase I/II Safety and Efficacy Study of AAV-SLC4A11 Vector to Treat Congenital Hereditary Endothelial Dystrophy (CHED)

 

Santen Pharmaceuticals Logo

Santen Pharmaceuticals

Role:               Site Principal Investigator
Duration:         02/02/23-02/01/25
Description:     A Phase 2a, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group, Multicenter Study Assessing the Efficacy and Safety of STN1010904 Ophthalmic Suspension 0.03% and 0.1% Compared with Vehicle in Subjects with Fuchs endothelial corneal dystrophy

 

 

Doug Chung, PhD

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Eye Bank Association of America

Role:               Principal Investigator
Duration:         07/01/23-06/30/24
Description:     Characterizing the transcriptomic profiles of cultured ex vivo corneal endothelial cells treated with mitochondria-targeted antioxidants during cell expansion

 

Wenlin Zhang, MD, PhD

Foundation for the National Institutes of Health

Foundation for the National Institutes of Health
Accelerating Medicines Partnership® (AMP®) Bespoke Gene Therapy Consortium (BGTC)

Role:               Co-Principal Investigator
Duration:         05/28/23-05/27/28
Description:     Phase I/II Safety and Efficacy Study of AAV-SLC4A11 Vector to Treat Congenital Hereditary Endothelial Dystrophy (CHED)

 

California's Stem Cell Agency Logo

California Institute for Regenerative Medicine

Role:               Co-Principal Investigator
Duration:         08/01/23-02/28/26
Description:     AAV gene therapy for treating congenital hereditary endothelial dystrophy associated with biallelic SLC4A11 mutations