Curated News
By: NewsRamp Editorial Staff
July 01, 2025
FELIQS Secures $9M to Advance Pediatric Retinal Disease Treatment
TLDR
- FELIQS Corporation secures $9 million Series A funding to advance FLQ-101, offering a competitive edge in treating rare pediatric retinal diseases with its innovative approach.
- FELIQS Corporation's FLQ-101, a once-daily oral or intravenous solution, targets retinopathy of prematurity by enhancing retinal vascularization and preventing abnormal neovascularization, with Phase 1b/2 studies starting in 2025.
- FELIQS Corporation's breakthrough in pediatric retinal disease treatment with FLQ-101 promises a brighter future for premature infants at risk of blindness, addressing a critical unmet need in neonatal care.
- Discover how FELIQS Corporation's FLQ-101, backed by $9 million funding, is set to revolutionize treatment for retinopathy of prematurity, a leading cause of childhood blindness.
Impact - Why it Matters
This news is significant because it highlights a major advancement in the treatment of retinopathy of prematurity, a condition that can lead to blindness in premature infants. The development of FLQ-101 represents hope for families and healthcare providers dealing with this challenging condition, offering a potential solution where few exist. The investment and regulatory support underscore the therapy's potential to fill a critical gap in neonatal care, promising to improve outcomes for vulnerable newborns worldwide.
Summary
FELIQS Corporation, a pioneering biotechnology firm based in Fukuoka, Japan, has successfully secured $9 million in Series A funding. This significant financial boost was co-led by a prominent American pharmaceutical company and Beyond Next Ventures Inc., with contributions from the Japan Science and Technology Agency and existing investors. The funding is earmarked to accelerate the clinical development of FLQ-101, FELIQS's flagship treatment for retinopathy of prematurity (ROP), a rare pediatric retinal disease. FLQ-101, which has already received Fast Track and Orphan Drug designations from the U.S. FDA, is a groundbreaking once-daily oral or intravenous solution aimed at promoting healthy retinal vascularization and combating inflammation and abnormal neovascularization. The Phase 1b/2 tROPhy-1 study is set to begin in the U.S. in summer 2025, marking a critical step forward in addressing a pressing unmet need in neonatal care.
Dr. Ken-ichiro (Nobu) Kuninobu, Co-Founder and CEO of FELIQS, expressed gratitude for the investment, highlighting its role in advancing the company's mission to develop targeted treatments for underserved pediatric populations. The proceeds will also support the expansion of FELIQS's operational and clinical teams, as well as bolster collaborative research efforts in the U.S. Founded in 2019, FELIQS specializes in creating first-in-class small molecule therapeutics that target oxidized lipids, with a focus on rare pediatric retinal diseases. The company's innovative approach and commitment to tackling challenging medical conditions underscore its potential to make a lasting impact in the field of ophthalmology.
Source Statement
This curated news summary relied on content disributed by Reportable. Read the original source here, FELIQS Secures $9M to Advance Pediatric Retinal Disease Treatment
