Last update 08 May 2025

Recombinant AAV-8 vector encoding human SLC4A11 variant B protein (UCLA)

Overview

Basic Info

Drug Type
AAV based gene therapy
Synonyms
Recombinant Adeno-Associated Virus 8 vector encoding human solute carrier family 4 member 11 variant B protein (UCLA)
Target
SLC4A11
Action
modulators
Mechanism
SLC4A11 modulators(solute carrier family 4 member 11 modulators)
Therapeutic Areas
Congenital DisordersEye Diseases
Active Indication
Corneal Dystrophies, Hereditary
Inactive Indication-
Originator Organization
University of California, Los AngelesUniversity of California, Los Angeles
Active Organization
University of California, Los AngelesUniversity of California, Los Angeles
Inactive Organization-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
RegulationOrphan Drug (United States)

Related

100 Clinical Results associated with Recombinant AAV-8 vector encoding human SLC4A11 variant B protein (UCLA)
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100 Translational Medicine associated with Recombinant AAV-8 vector encoding human SLC4A11 variant B protein (UCLA)
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100 Patents (Medical) associated with Recombinant AAV-8 vector encoding human SLC4A11 variant B protein (UCLA)
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100 Deals associated with Recombinant AAV-8 vector encoding human SLC4A11 variant B protein (UCLA)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Corneal Dystrophies, HereditaryPreclinical
United States
University of California, Los AngelesUniversity of California, Los Angeles
18 Sep 2024
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Clinical Result

Indication
Phase
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Approval

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Regulation

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