Privately-held Swiss company Ferring Pharmaceuticals and its subsidiary Rebiotix look set to achieve a notable first for the industry.
Their investigational microbiota-based live biotherapeutic RBX2660 - also known as Rebyota - is on the brink of becoming the first microbiome-based therapy to gain a regulatory approval.
Ferring is seeking US Food and Drug Administration (FDA) approval for this fecal microbiota suspension - which is prepared from human stool collected from pre-screened, qualified donors and administered rectally by enema - to reduce recurrence of C. difficile infection (CDI) after antibiotic treatment.
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