USA-based drug developer Biovest International says that it has received approval from the Russian Ministry of Health and Social Development of the Russian Federation to recruit patients for enrollment in a Phase III trial of its anticancer agent BiovaxID. The approval, which extends to 14 new clinical trial sites in the country, will allow the accelerated enrollment of patients into the ongoing trial program.
Biovest said that it expects to recruit a further 175 patients from the new sites over the next 18months. The firm added that enrollment and logistics would be coordinated by ClinStar Europe, a regional subsidiary of the US clinical trials firm.
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