Country for PR: China
Contributor: PR Newswire Asia (China)
Tuesday, November 08 2022 - 11:00
AsiaNet
Cyagen and Neurophth Enter Global Strategic Collaboration to Develop AI-Designed AAV Gene Therapy Vectors for Ophthalmic Disorders
SANTA CLARA, Calif., Nov. 3, 2022 /PRNewswire-Asianet/ --

Cyagen today announced a strategic collaboration with Neurophth Therapeutics, 
Inc. to co-develop next-generation AAV gene therapy vectors for specific types 
of genetic ophthalmic disorders.

Under the terms of the agreement,Cyagen will apply its proprietary artificial 
intelligence (AI)-powered high-throughput platform to discover novel AAV 
vectors with optimized tissue targeting capability,tissue specificity,and 
productivity. Cyagen and Neurophth will both be responsible for evaluating the 
functional properties of the novel AAV vectors in rodent and NHP models, and 
Neurophth will be responsible for conducting clinical trials and 
commercialization for gene therapy products developed using Cyagen's novel AAV 
capsids. Cyagen could receive research phase and clinical phase milestone 
payments, as well as sales royalties that may exceed $140 million.

Solving the Challenges of Gene Therapy Research and Development

Utilizing AI and single-cell RNA-sequencing technologies, Cyagen's 
high-throughput AAV vector discovery platform helps overcome the present 
limitations of gene therapy R&D by quickly identifying next-generation AAV 
capsids that have enhanced tissue targeting capability, tissue specificity, and 
productivity. Cyagen has produced substantial experimental data for AI model 
training and developed proprietary machine learning algorithms to accelerate 
the AAV capsid identification and optimization processes compared to 
traditional directed evolution methods.

Recognizing the growing potential for ophthalmic gene therapy, Cyagen's 
Ophthalmology Research Solution platform is fully equipped with 
state-of-the-art ophthalmic instruments and an experienced professional team.

"Gene therapy has demonstrated great promise and potential for treating genetic 
ophthalmic diseases, and the ophthalmic gene therapy market has expanded 
exponentially in the past few years," Lance Han, president of Cyagen, said. 
"Together with Neurophth, we will develop the world's best AAV ophthalmic gene 
therapy products and bring brightness back to patients all over the world."

"Neurophth hopes to seek like-minded partners to work together to achieve 
breakthroughs in ophthalmic gene therapy development, and I think Cyagen is our 
ideal companion on the road ahead," said Bin Li, Founder, Chairman and CEO of 
Neurophth.

About Cyagen
Founded in 2006, Cyagen is a global provider of genetically modified rodent 
models and innovative one-stop cell and gene therapy solutions for R&D, 
including: disease model development, AAV discovery, drug efficacy studies, and 
more. Cyagen currently has over 900 employees and multiple facilities with a 
total scale of over 40,000 square meters. The company has established extensive 
cooperations with scientists and institutions in more than 100 countries, 
leading to the publication of over 6,300 academic articles-including the three 
major journals of CNS (Cell, Nature, Science). From its foundation in animal 
model development, to implementation of AI-powered tools for data analysis and 
therapeutic discoveries, Cyagen provides one-stop solutions for accelerating 
basic research and new drug R&D with our unique offering of models, data, 
algorithms, and services.

About Neurophth
Neurophth is China's leading gene therapy company focusing on ophthalmic 
diseases. NR082 (NFS-01), Neurophth' core product, designed to treat 
ND4-mediated Leber's hereditary optic neuropathy (ND4-LHON), has been granted 
Orphan Drug Designation (ODD) by the US Food and Drug Administration (FDA) and 
the European Medicines Agency (EMA), and is the first Chinese gene therapy new 
drug that has been granted IND approval for clinical trials by Chinese National 
Medical Products Administration (NMPA) and the US FDA. At present, the first 
patient has been dosed in the Phase III clinical trial in September 2022. The 
company's pipeline also includes ND1-mediated LHON (the company's second new 
drug with ODD granted by the US FDA), autosomal dominant optic atrophy, optic 
nerve protection, vascular retinopathy and other preclinical candidates.

2255 Martin Avenue,Suite E,Santa Clara,CA 95050-2709,US
800-921-8930(8-6pm PST) 
animal-service@cyagen.com

SOURCE:Cyagen Biomodels LLC

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