Eyestem’s Dr. Jogin Desai 
Precision Medicine

Eyestem’s Dr. Jogin Desai Presents Landmark Phase 1 Results of Eyecyte-RPE™ Trial at Innoxbio CGT 2025 in Guangzhou, China

By Team VOH

Guangzhou, China | November 13, 2025: Eyestem Research Pvt. Ltd., a clinical-stage biotechnology company pioneering scalable cell therapy solutions for retinal diseases, announced the successful presentation of its groundbreaking phase one clinical trial results at the 3rd China Great Bay Cell and Gene Therapy Forum (Innoxbio CGT 2025), held on November 12–13, 2025, in Guangzhou Knowledge City. Innoxbio China Great Bay  CGT Forum  is recognized as one of the most influential global gatherings for leaders in cell and gene therapy.

Eyestem is preparing to initiate its Phase 2 clinical trial in India, subject to regulatory approvals. The company is also exploring licensing partnerships in China to advance the local development and commercialization of Eyecyte-RPE™, its flagship cell therapy. Trials in the United States are expected to commence by the middle of  next year.

Sharing key findings from Eyestem’s Phase 1 study, Dr. Jogin Desai, Founder and CEO of Eyestem, presented onSafety and Efficacy of Eyecyte-RPE™ in a Phase 1 Trial for Treatment of Geographic Atrophy Secondary to Dry AMD.”

The trial demonstrated an average improvement of 14.8 letters in visual acuity among eight subjects at six months, and 13.3 letters in four subjects at 12 months, with no treatment related serious adverse events observed. These results underscore the strong potential of Eyestem’s investigational retinal pigment epithelium (RPE) cell therapy, Eyecyte-RPE™, to transform treatment outcomes for patients suffering from geographic atrophy (GA), an advanced form of dry age-related macular degeneration (AMD).

Commenting on the milestone, Dr. Desai said, “Our phase one study demonstrates clinically meaningful vision rescue with an excellent safety profile, a promising step toward addressing a condition with no current approved treatments that can reverse vision loss. As we prepare to begin phase two in India and file for US IND approval in Q3 2026, we are also exploring strategic partnerships to bring this breakthrough to global markets. Collaborating with international stakeholders is crucial to our mission of making world-class, affordable cell therapies accessible to patients everywhere.”

The forum brought together over 1,200 experts, 90+ leading speakers, and 50 exhibitors, providing a platform for collaboration across the global cell and gene therapy ecosystem. Dr. Desai’s session was part of the Ophthalmology and Rare Diseases track, highlighting the vital role of regenerative medicine in addressing unmet needs in vision care.

Also Read

SCROLL FOR NEXT