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Genetic: AAV5-hRKp.RPGR Intermediate Dose

Janssen Research & Development, LLC · Phase 3 active Biologic

AAV5-hRKp.RPGR is a gene therapy that delivers a functional copy of the RPGR gene into retinal cells to restore vision in patients with X-linked retinitis pigmentosa.

AAV5-hRKp.RPGR is a gene therapy that delivers a functional copy of the RPGR gene into retinal cells to restore vision in patients with X-linked retinitis pigmentosa. Used for X-linked retinitis pigmentosa (XLRP) caused by RPGR mutations.

At a glance

Generic nameGenetic: AAV5-hRKp.RPGR Intermediate Dose
Also known asbotaretigene sparoparvovec
SponsorJanssen Research & Development, LLC
Drug classGene therapy (AAV vector)
TargetRPGR (retinitis pigmentosa GTPase regulator) gene
ModalityBiologic
Therapeutic areaOphthalmology / Retinal Diseases
PhasePhase 3

Mechanism of action

This adeno-associated virus (AAV5) vector carries the human RPGR (retinitis pigmentosa GTPase regulator) gene under control of a photoreceptor-specific promoter. The therapy is administered via subretinal injection to transduce photoreceptor cells, enabling them to produce functional RPGR protein and halt or reverse photoreceptor degeneration. This addresses the genetic defect underlying X-linked retinitis pigmentosa, a progressive inherited retinal dystrophy.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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