BioBlast® - Search
EU | EU grants marketing authorisation for Tysabri® SC (natalizumab)
April 7, 2021
Biogen announced the EC has granted marketing authorisation for Tysabri® (natalizumab) in a subcutaneous presentation. Tysabri® SC is approved for the treatment of relapsing-remitting multiple sclerosis.
Novartis provides updates on Sandoz biosimilar candidates
November 24, 2020
Novartis released its annual report ‘Meet Novartis Management 2020‘. In the report, Novartis announced that GP2411 (biosimilar denosumab candidate) has commenced Ph III trials. Novartis has also indicated it has planned launches for biosimilar adalimumab and natalizumab in 2021-2023 and denosumab in 2024-2026.
New study demonstrates efficacy of natalizumab in MS
September 10, 2020
Neurology Advisor reported a new study indicates that natalizumab may be more effective than fingolimod or BRACETD in reducing relapses in patients with relapsing-remitting multiple sclerosis.
Phase III trials of natalizumab biosimilar commence
November 18, 2019
Polpharma commences dosing in Phase III trials of proposed natalizumab biosimilar.
Details of clinical trials of biosimilar natalizumab candidate published
October 13, 2019
Polpharma publishes details of upcoming phase III clinical trials of biosimilar natalizumab candidate. The study will involve approximately 260 patients with relapsing-remitting multiple sclerosis.
Pfizer and Polpharma licensing deal for natalizumab biosimilar
September 3, 2019
Pfizer and Polpharma announce licensing deal for natalizumab biosimilar. Under the agreement, Polpharma will develop, manufacture and supply the product, while Sandoz will be responsible for commercialisation and distribution.
Product specific reports based on extracts from our BioBlast® database
BioBlast® Editor and Contributing Author
Get our Pearce IP Blogs & BioBlast® sent directly to your inbox
Subscribe to our Pearce IP Blogs and BioBlast® to receive our updates via email.