(Removes reference to inoperable tumours in 1st paragraph)
LONDON, Sept 16 (Reuters) - An experimental Northwest
Biotherapeutics NWBO.O drug for brain tumours is the first
medicine to have been selected for fast-track designation under
a new early access scheme in Britain.
The U.S. firm's cell therapy DCVax-L has been awarded
"promising innovative medicine" status, which is the first step
in the scheme that allows access to novel drugs months or even
years before they are officially licensed for sale, the
department of health said on Tuesday.
The initiative, which has similarities with a U.S. scheme
that has speeded the development of so-called "breakthrough"
medicines, follows criticism that Britain's state-run healthcare
system is too slow to adopt new treatments. ID:nL6N0MA43O
Doctors will be able to prescribe the new drug once the
Medicines and Healthcare Products Regulatory Agency, the
country's drugs watchdog, signals that its benefits outweigh the
risks following an initial scientific assessment.
The new early access programme is funded by drug companies.
(Reporting by Ben Hirschler; editing by Jason Neely)
((ben.hirschler@thomsonreuters.com; +44 20 7542 5082; Reuters
Messaging: ben.hirschler.thomsonreuters.com@reuters.net))