Gene Therapies
OCU400
In five unique mouse models of Retinitis Pigmentosa (RP), treatment with the AAV-NR2E3 gene by subretinal injection rescued multiple genetically diverse IRDs by protecting photoreceptors from further damage after disease onset. The five RP models tested were rd1 (PDE6β associated RP), Rho-/- and RhoP23H (both Rhodopsin associated RP), rd16 (Leber Congenital Amaurosis) and rd7 (Enhanced S-cone Syndrome). The study, published in Nature Gene Therapy, demonstrates the potential of a novel modifier gene therapy to elicit broad-spectrum therapeutic benefits in early and intermediate stages of RP and Leber Congenital Amaurosis (LCA) based on animal models, showing the potential for a mutation-agnostic treatment.
Currently, Ocugen is developing OCU400 for the treatment of multiple IRDs encompassing RP and LCA.
EARLY DISEASE STAGE

ADVANCED DISEASE STAGE

OCU400 Publications
- Li, S., Datta, S., Brabbit, E. et al. Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa. Gene Ther (2020).
- Haider, N. B. et al. Mapping of genetic modifiers of Nr2e3rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity. Mammalian Genome 19, 145-154, 2008.
- Olivares, A. M. & Haider, N. B. Role of Nuclear Receptors in Central Nervous System Development and Associated Diseases. 9, 93-121, (2015).
- Cheng, H. et al. In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development. Hum Mol Genet 15, 2588-2602, (2006).
- Haider, N. B. et al. The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation. Visual Neuroscience 23, 917-929, (2006).
- Schorderet, D. F. & Escher, P. NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP). Human Mutation 30, 1475-1485, (2009).
OCU410

OCU410ST
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