New data has shown Esbriet (pirfenidone) from Swiss drug giant Roche’s (ROG: SIX) Genentech unit can reduce risk of death in idiopathic pulmonary fibrosis (IPF) patients by up to 38% if they stay on the treatment for up to two years, compared to placebo.
Previously-reported data from a trial at one year showed the risk of mortality was reduced by 48% after treatment with Esbriet, a statistically significant result. The new data at 120 weeks show a strong trend in a reduced risk of death with long-term Esbriet treatment in IPF, according to Roche.
Ben Kramer, vice president of medical affairs at Genentech, explained why Esbriet works, if not precisely how. He said: “We know that Esbriet has an anti-fibrotic effect,” but “We don’t know exactly how that happens, we don’t know the exact mechanism of action. But we know from research that it has this anti-fibrotic effect and that’s the main problem for IPF patients- they develop fibrosis in their lungs, and that leads to death.”
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 2024 | Headless Content Management with Blaze