罗氏（Roche）近日宣布，美国FDA已批准Susvimo（ranibizumab）用于治疗糖尿病性黄斑水肿（DME）。据悉，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也是首个持续 ...

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 ...

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--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 Susvimo ...

The Food and Drug Administration (FDA) has approved Susvimo ® (ranibizumab injection) for the treatment of patients with diabetic macular edema (DME) who have previously responded to at least 2 ...

RCT = prospective randomized controlled; RVO = retinal vein occlusion; IVR = intravitreal ranibizumab; M = multicenter; CRVO = central retinal vein occlusion; BCVA = best-corrected visual acuity ...

Topline results for COAST are anticipated in early Q2 2025, with ShORe results expected mid-2025.

COAST Phase 3 trial evaluates superiority and safety of sozinibercept combined with aflibercept in wet AMDCompany confirms topline results for ...

Sold as Susvimo, it's the first device that slowly releases ranibizumab, a medicine that treats eye diseases, so patients don’t need frequent injections. DME affects about 750,000 people in the ...

Background: To identify differences between Ranibizumab and Aflibercept in treatment-naïve patients with neovascular age-related macular degeneration (nvAMD) in a real-life clinical setting.

Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that the US Food and Drug Administration (FDA) has approved Susvimo® (ranibizumab injection) 100 mg/mL for the treatment of diabetic macular edema ...