Ray Therapeutics imagery representing the development of RTx-021, an optogenetic gene therapy for Stargardt disease.
Ray Therapeutics has announced a CIRM grant for RTx-021, its optogenetic gene therapy for Stargardt disease. The funding will support clinical development and manufacturing work.

Ray Therapeutics has announced new funding from the California Institute for Regenerative Medicine (CIRM) to advance RTx-021, its optogenetic gene therapy being developed for Stargardt disease. Ray described the award as an $8 million grant in its September 30 announcement. CIRM’s governing board had approved $7,935,162 for the project on September 25.

The funding will support the ongoing Phase 1/2 clinical study of RTx-021 and manufacturing activities intended to prepare the program for later-stage development. RTx-021 is being evaluated in an open-label, dose-escalation study in patients with Stargardt disease and is designed to target retinal bipolar cells through a single intravitreal injection.

Founded in 2021 and based in Berkeley, California, Ray Therapeutics is a clinical-stage biotechnology company developing optogenetic therapies for degenerative retinal diseases. Its approach uses bioengineered light-sensitive proteins delivered to surviving retinal cells with the aim of improving visual function independently of the underlying genetic mutation. Paul Bresge is the company’s CEO and co-founder.

Ray’s pipeline also includes RTx-015, an optogenetic gene therapy being developed for retinitis pigmentosa and other inherited retinal diseases. In April 2026, the company closed a $125 million Series B financing led by Janus Henderson Investors to support development of RTx-015 and RTx-021.

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