Breakthrough in diabetes care: Roche’s Susvimo could revolutionize eye treatment

Pallavi Madhiraju- July 20, 2024 0

Roche, a global leader in pharmaceuticals and diagnostics, recently unveiled two-year data from the pivotal Phase III Pagoda and Pavilion studies, showcasing the sustained efficacy ... Read More

FDA approves Roche’s Vabysmo prefilled syringe for eye diseases, expanding treatment options for millions

Pallavi Madhiraju- July 7, 2024 0

Roche (SIX: RO, ROG; OTCQX: RHHBY), a global leader in pharmaceuticals and diagnostics, announced a significant advancement in eye care with the U.S. Food and ... Read More

FDA approves Genentech’s Vabysmo prefilled syringe for eye diseases

Pallavi Madhiraju- July 5, 2024 0

In a significant advancement in the treatment of eye diseases, the U.S. Food and Drug Administration (FDA) has approved Genentech's Vabysmo (faricimab-svoa) 6.0 mg single-dose ... Read More

Rezolute’s Phase 2 trial of RZ402 shows significant CST reduction in DME patients

Pallavi Madhiraju- May 22, 2024 0

Rezolute, Inc. (Nasdaq: RZLT), a leader in the development of novel therapies for serious metabolic and rare diseases, today disclosed promising topline results from its ... Read More

KSI-301 phase 1b trial : Kodiak Sciences reports new safety, efficacy, and durability data

pharmanewsdaily- July 11, 2020 0

KSI-301 phase 1b trial : Kodiak Sciences said that its ongoing phase 1b clinical trial of its intravitreal anti-VEGF antibody biopolymer conjugate KSI-301 for the ... Read More

Kodiak Sciences completes enrollment for KSI-301 safety study in retinal disease

pharmanewsdaily- September 2, 2018 0

Kodiak Sciences, a California-based biotechnology company, has recently completed patient enrollment for a phase 1 safety and tolerability study of its innovative retinal disease drug, ... Read More

FDA approves Genentech’s lucentis for comprehensive diabetic retinopathy treatment

pharmanewsdaily- April 23, 2017 0

Genentech, a member of the Roche Group, has received approval from the U.S. Food and Drug Administration (FDA) for its lucentis (ranibizumab injection), making it ... Read More