THE Russian Federal Service on
Surveillance in Healthcare and
Social Development has become
the first agency to approve Merck
Serono’s Movectro (oral cladribine)
for the treatment of relapseremitting
MS (RRMS) patients.
The world’s first oral diseasemodifying
MS therapy, the drug is
set to take on the market leading
interferon betas and Copaxone
(glatiramer acetate, Teva) MS
treatments.
In the US, Novartis’ own oral
disease-modifying MS therapy
Gilenia (fingolimod) is set to beat
Movectro to the market, having
already received unanimous
backing by the FDA advisory panel
for the treatment of relapse-remitting
MS (RRMS) patients, back in June.
At present Movectro has not yet
received the US FDA advisory panel
nod.The above article was sent to subscribers in Pharmacy Daily's issue from 16 Jul 10 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 16 Jul 10
MAYNE Pharma Group Limited has filed a patent infringement suit against Sun Pharmaceutical Industries Ltd and Inc., in the United States District Court, according to yesterday’s ASX announcement.
PHARMACY Connect 2024 conference will feature a provocative ‘Great Debate’ during the Harm Minimisation Workshop on Thu 05 Sep at the Hyatt Regency in Sydney.
LTR Pharma Limited has successfully raised $10.5 million through a share placement to sophisticated and new institutional investors, significantly surpassing initial demand.
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