Bayer Eylea approved in Japan for treatment of preterm infants with retinopathy of prematurity
Retinopathy of prematurity is a rare eye disease that affects the vessels in the retina of premature infants and is the leading cause of visual impairment and blindness in children.;
Berlin: Bayer has announced that the Ministry of Health, Labour and Welfare (MHLW) in Japan has approved Eylea (aflibercept) intravitreal injection 40 mg/mL for the treatment of preterm infants with retinopathy of prematurity (ROP).
"Retinopathy of prematurity is a disease that affects premature infants and severe forms can lead to significant visual impairment and even blindness. Timely treatment in this vulnerable pediatric patient population is crucial," said Dr. Michael Devoy, Chief Medical Officer at Bayer. "It is estimated that in Japan approximately 1,000 to 2,000 premature infants per year require treatment for ROP and with Eylea we can now offer an additional therapeutic option for patients and healthcare professionals in Japan."
"The FIREFLEYE study was the first randomized clinical trial that compared the effects of Eylea to laser in the treatment of patients with severe ROP worldwide. The trial data provide us with prospective and clinically relevant evidence. Treatment success with Eylea 0.4 mg was high as expected and achieved with mostly a single injection per eye," said Dr. Noriyuki Azuma, investigator of the FIREFLEYE study and president of the Japanese Association of Pediatric Ophthalmology.
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