Roche, Susvimo and FDA

FDA expands label for Roche's eye disease implant Susvimo
The new indication adds to the 2021 approval of Susvimo (ranibizumab) for 'wet' or neovascular age-related macular degeneration (AMD), and comes just a few months after Roche returned the drug to the US market after a two-year hiatus.
Roche gains label expansion for eye implant Susvimo to treat diabetic macular edema
Seven months after the FDA signed off on a reintroduction of Roche’s eye implant Susvimo, the U.S. regulator has broadened its label as a treatment for diabetic macular edema (DME), which is the leading cause of diabetes-related blindness.
FDA approves Roche’s Susvimo for DME
The US Food and Drug Administration (FDA) has approved Susvimo (ranibizumab injection) 100mg/mL for the treatment of diabetic macular edema (DME), said Swiss pharma giant Roche.
FDA approves Roche’s Susvimo as the first and only continuous delivery treatment for the leading cause of diabetes-related blindness
Susvimo is the first and only continuous delivery treatment that offers an alternative to regular eye injections to treat diabetic macular edema (DME)With as few as two treatments per year, Susvimo may help people with DME maintain their visionApproval marks the second indication for Susvimo in addition to neovascular or ‘wet’ age-related macular degeneration (nAMD) Basel,
FDA Approves Roche’s Susvimo Refillable Eye Implant for Diabetic Macular Edema
Roche’s Susvimo, a refillable eye implant for diabetic macular edema, provides continuous delivery of ranibizumab, showing sustained vision improvements with fewer treatments than standard eye injections.
Roche announces FDA approves Susvimo to treat DME
Roche (RHHBY) announced that the Food and Drug Administration has approved Susvimo 100 mg/mL for the treatment of diabetic macular edema, a
Roche's Susvimo gets FDA approval for diabetic macular edema
Genentech unit has received FDA approval for its drug Susvimo 100 mg/mL injection for the treatment of diabetic macular edema, a leading cause of blindness for people with diabetes. Susvimo, also known as ranibizumab injection,
FDA Approves Genentech’s Susvimo as the First and Only Continuous Delivery Treatment for the Leading Cause of Diabetes-Related Blindness
Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY) announced today that the U.S. Food and Drug Administration (FDA) has approved Susv
Genentech : FDA Approves Susvimo For Diabetic Macular Edema Treatment
Genentech, a member of the Roche Group (RHHBY), announced that the U.S. Food and Drug Administration has approved Susvimo
Roche: FDA Approves Susvimo for Treatment of Diabetic Macular Edema
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With FDA approval, Genentech turns eye implant's focus to diabetes
Genentech initially won Food and Drug Administration approval of the refillable implant in 2021 for patients with we
每两年一次，95%患者无需额外治疗！罗氏创新疗法获FDA批准
罗氏（Roche）今日宣布，美国FDA已批准Susvimo（ranibizumab）用于治疗糖尿病性黄斑水肿（DME）。根据新闻稿，Susvimo是首个经FDA批准、可通过比常规眼内注射更少的治疗次数来维持视力的DME疗法。此外，Susvimo也是首 ...
腾讯网17h
刚刚！FDA批准罗氏Susvimo用于糖尿病黄斑水肿治疗：1年仅需2次
医脉通编译撰写，未经授权请勿转载。导语每月一针太痛苦？糖尿病黄斑水肿治疗迎来新突破！美国时间2025年2月4日，罗氏公司（Roche）官网发布消息，美国食品药品监督管理局（FDA）已批准Susvimo（Port Delivery Platform with ranibizumab）100 ...