A framed image of two shaking hands, symbolizing the collaboration of PolyActiva and RareSight. Both company logos appear above the handshake.

PolyActiva and RareSight Join Forces to Target Rare Pediatric Retinal Diseases

In a move that could reshape how IRDs are treated, two innovative companies are joining forces to make long-lasting vision therapies a reality. 

PolyActiva (Victoria, Australia) and RareSight (California, USA) have announced a strategic collaboration to co-develop sustained-release therapies for rare pediatric retinal diseases, marking PolyActiva’s expansion into new ophthalmic indications beyond glaucoma. 

“This collaboration represents an important step in PolyActiva’s growth as we expand our proprietary platform into new therapeutic areas,” said PolyActiva CEO and Board Director Jerry St. Peter in a news release. “Partnering with RareSight allows us to apply our PREZIA technology beyond glaucoma to address the urgent unmet needs of children living with inherited retinal disorders. This effort reflects our broader vision to build a diversified ophthalmic pipeline that delivers durable, targeted and potentially life-changing treatments for people who have long been overlooked.”

 

Joint focus on long-acting delivery

The partnership will harness PolyActiva’s biodegradable sustain-release implant platform and RareSight’s therapeutic discovery capabilities to address inherited retinal diseases (IRDs) that affect children. The companies plan to develop long-acting pharmacologic therapies capable of maintaining intraocular drug delivery for extended duration, minimizing the need for repeated procedures. 

READ MORE: Glimmers of Hope: Next-Gen Pediatric Retina Care Promises to Deliver Solutions Once Deemed Out of Reach

“At RareSight, we are dedicated to preventing sight loss caused by rare pediatric eye diseases,” said RareSight CEO and Founder Carmen Caricchio. “By combining RareSight’s therapeutic discovery and development expertise with PolyActiva’s novel drug delivery platform, this collaboration represents a major step toward transforming how inherited eye diseases are treated. Together, we are advancing a new class of long-acting pharmacologic therapies to address early-onset vision loss, with the potential to change a child’s life and bring hope to generations to come.”

Retinal and Optic Nerve Diseases Easy to Diagnose in Children with RETeval ERG device

The two companies have not disclosed specific molecules or timelines for initial clinical evaluation, but early-stage formulation and feasibility studies are underway. 

According to IRD specialist Dr. Sandeep Grover, “As a pioneer of the earliest research in this field and caring for kids and their families for more than two decades, I am encouraged by novel therapeutic strategies that support our goal of helping patients maintain vision, function and independence as long as possible.”

READ MORE: Gene Therapy Shows Promise for AIPL1-Associated Retinal Dystrophy in Children

PolyActiva’s portfolio

The collaboration with RareSight expands PolyActiva’s clinical-stage ophthalmic portfolio, which includes PA5108, a new chemical entity and biodegradable ocular micro-implant developed for sustained intraocular pressure control of up to six months using the PREZIA platform. The Phase IIb U.S. study, involving about 75 patients across 12 sites, is currently evaluating the implant’s safety, tolerability and durability over time. 

By extending this proprietary pro-drug technology into new therapeutic areas, including rare pediatric retinal diseases, the two companies aim to bring forward much-needed drug-based options for underserved patient groups. 

READ MORE: MacuMira and Keeler Join Forces to Advance Non-Invasive Dry AMD Treatment Worldwide

Editor’s Note: This content is intended exclusively for healthcare professionals. It is not intended for the general public. Products or therapies discussed may not be registered or approved in all jurisdictions, including Singapore.

Subscribe
Notify of
guest
0 Comments
Oldest
Newest Most Voted
Inline Feedbacks
View all comments