A new Medicare analysis conducted by Johns Hopkins University in the USA was presented yesterday at the Association for Research in Vision and Ophthalmology (ARVO) meeting, highlighting the relative safety of Novartis’ (NOVN: VX) and fellow Swiss drug major Roche’s (ROG: SIX) Lucentis (ranibizumab) compared to Roche’s Avastin (bevacizumab).
The study by Gower et al from Johns Hopkins University is a retrospective database analysis that includes 77,886 Medicare beneficiaries to compare safety of unlicensed intravitreal Avastin compared to Lucentis in patients with wet age-related macular degeneration (AMD). The study was funded by Roche’s subsidiary Genentech.
Over 10 months, patients with wet AMD treated with unlicensed intravitreal Avastin experienced an 11% increased risk of death and a 57% increased risk of hemorrhagic stroke compared to those treated with Lucentis. There were no statistically significant differences in heart attack and ischemic stroke.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze