Retinitis Pigmentosa Treatment Market Driven by Gene Therapy Progress and Increased Research Funding 2025-2033 | Spark Therapeutics, Inc., jCyte, Inc., Coave Therapeutics, Kiora Pharmaceuticals, Inc.

Retinitis Pigmentosa Treatment Market size reached US$ 5.72 Billion in 2024 and is expected to reach US$ 11.13 Billion by 2033, growing at a CAGR of 7.7% during the forecast period 2025-2033.

Retinitis Pigmentosa Treatment Market Report by DataM Intelligence offers a detailed assessment of the global pharmaceutical and healthcare landscape, highlighting market size, key players, and critical growth drivers. With a focus on emerging drug technologies, evolving treatment paradigms, and regulatory frameworks, the report delivers strategic insights to support stakeholders in navigating the rapidly advancing sector from 2025 to 2033.

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Retinitis pigmentosa is a group of inherited retinal disorders causing progressive vision loss due to photoreceptor degeneration. The treatment market is expanding with the emergence of gene therapies, retinal implants, and neuroprotective agents, alongside rising investment in precision ophthalmology for rare genetic eye diseases.

Retinitis Pigmentosa Treatment Market Competitors Overview:

Spark Therapeutics, Inc., jCyte, Inc., Coave Therapeutics, Kiora Pharmaceuticals, Inc., Aldeyra Therapeutics, Inc., Beacon Therapeutics, ViGeneron GmbH, Nanoscope Therapeutics Inc., SparingVision, Inc., and Endogena Therapeutics Inc., among others.

Important Industry Updates of 2023, 2024 and 2025:

✅ In January 2025, ViGeneron GmbH, a next-generation clinical-stage gene therapy company, announced two important milestones for its novel gene therapy candidate VG901, to treat patients with retinitis pigmentosa (RP) caused by mutations in the CNGA1 gene. The U.S. Food and Drug Administration (FDA) has granted Rare Pediatric Disease Designation (RPDD) to VG901, and the independent Data Safety Monitoring Board (DSMB) has unanimously approved dose escalation in the ongoing Phase 1b clinical trial.

✅ In August 2024, Ocugen, Inc., a biotechnology company focused on discovering, developing, and commercializing novel gene and cell therapies and vaccines, today announced that Health Canada provided a "No Objection Letter" to initiate the OCU400 Phase III liMeliGhT clinical trial in Canada. OCU400 is a modifier gene therapy product candidate being developed for retinitis pigmentosa (RP).

Methodology and Scope

The Retinitis Pigmentosa Treatment Market Report is built on a rigorous research methodology that integrates primary interviews, expert insights, and validated secondary data from company reports, industry publications, and reliable databases. Utilizing both bottom-up and top-down approaches, the analysis ensures high data accuracy through triangulation. The report covers current market dynamics, growth opportunities, and key strategic developments across global and regional markets.

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Retinitis Pigmentosa Treatment Market Segments Overview:

∎ By Disease Type(Non-Syndromic Retinitis Pigmentosa, Syndromic Retinitis Pigmentosa)
∎ By Treatment Type (Gene Therapy, Vision Rehabilitation, Sunglasses, Vitamin A Supplements, Omega-3 Fatty Acids, Surgery, Others)

Regional Overview for Retinitis Pigmentosa Treatment Market:

⇥ North America (U.S., Canada, Mexico)
⇥ Europe (U.K., Italy, Germany, Russia, France, Spain, The Netherlands and Rest of Europe)
⇥ Asia-Pacific (India, Japan, China, South Korea, Australia, Indonesia Rest of Asia Pacific)
⇥ South America (Colombia, Brazil, Argentina, Rest of South America)
⇥ Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of Middle East & Africa)

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