Gemini Therapeutics Enrolls First Patient in Phase 1 Study of GEM103 for Dry Age-related Macular Degeneration

“Gemini was founded to deliver precision medicines for eye disorders by combining genetic insights with clinical and biological expertise in complement. We are excited to take GEM103 into the clinic as a novel approach in complement modulation for a devastating disease with no therapeutic options,” said Jason Meyenburg, Chief Executive Officer of Gemini. “We look forward to topline data from this study and the potential to initiate a Phase 2 study, supported by data from our ongoing CLARITY natural history study examining the pathogenesis and progression of dry AMD in patients carrying CFH risk variants.”

CFH risk variants are reported to occur in greater than 40% of patients with dry AMD and are strongly associated with the risk of developing the disease. The complement system, of which CFH is a modulator, is dysregulated in patients with these risk variants and results in amplification of aberrant inflammatory responses in the eye. Over time this dysregulation leads to damage to the macular region of the retina. GEM103 is a fully functional recombinant native CFH protein intended to address dysregulation caused by loss of CFH function variants in the eyes of these AMD patients.

“The management of dry AMD, due to its prevalence and pronounced impact on the patient’s quality of life, continues to be a challenge as there are no treatment options available,” said Arshad Khanani, M.D., M.A., Managing Partner and Director of Clinical Research at Sierra Eye Associates, Reno, Nevada and an investigator in the study. “Clinicians are looking for breakthrough treatments to disrupt the pathology of dry AMD. The concept of treating genetically selected patients with GEM103 to potentially modulate and normalize the alternative complement pathway is an exciting approach.”

This study is a Phase 1 single ascending dose (SAD) clinical study evaluating the safety, pharmacokinetics and pharmacodynamics of GEM103. The study targets enrolment of approximately 9 patients with dry AMD who have known CFH mutations.

About Dry AMD
AMD is a progressive retinal disease affecting older adults, and the leading cause of irreversible blindness in the western world, affecting millions. Symptoms, including blurry vision, loss of night vision and loss of central vision, make activities of daily living such as reading, driving and even recognizing faces more difficult over time. Dry AMD results from an interaction of both environmental and genetic risk factors. Aging and smoking confer the strongest non-genetic risk, but genetic risk is significant, with approximately 70% attributable risk of advanced disease due to heritability. Research over the last decade has uncovered multiple genetic variants which can increase risk of developing advanced AMD by up to 20-fold. Gemini Therapeutics is examining many of these genetic variants through CLARITY, its natural history study in people with dry AMD.

Gemini Therapeutics
Gemini Therapeutics is a clinical stage precision medicine company developing innovative treatments for age-related macular degeneration (AMD) and linked ocular disorders that are matched to molecular abnormalities found in patients with high clinical unmet need. The company has generated a rich pipeline including recombinant proteins, monoclonal antibodies, and gene therapies. Gemini’s CLARITY natural history study is designed to provide unprecedented insight into the role of genetic risk in common retinal diseases and began in December 2018. Gemini was launched with funding from leading life science investors and powered by academic partnerships globally.

For more information, visit www.GeminiTherapeutics.com.

View source version on businesswire.com: https://www.businesswire.com/news/home/20200109005214/en/