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Portola's Andexxa bleeding antidote wins FDA nod but will see limited release
Portola's Andexxa bleeding antidote wins FDA nod but will see limited release
Portola has finally overcome FDA concerns to win approval of its coagulation factor Xa, a bleeding antidote for some of the new generation blood thinners like Xarelto and Eliquis.
South Africa's Aspen opens $80M high potency site, adding 500 workers
South Africa's Aspen opens $80M high potency site, adding 500 workers
South Africa’s Aspen Pharmacare is expanding into complex meds for cancer and other conditions and has just opened an $80 million facility that can produce them, adding about 500 jobs in the process...
Aurobindo bids $1.6B for Novartis' U.S. dermatology generics: report
Aurobindo bids $1.6B for Novartis' U.S. dermatology generics: report
As Novartis tries to shed some of its Sandoz offerings in the U.
Japan's Takeda clinches $62 billion deal to buy drugmaker Shire
Japan's Takeda clinches $62 billion deal to buy drugmaker Shire
Takeda Pharma agreed to buy London-listed Shire for 45.
Bayer sells further Covestro stake for 2.2 billion euros
Bayer sells further Covestro stake for 2.2 billion euros
BERLIN (Reuters) - Pharmaceutical group Bayer (BAYGn.
Sarepta Therapeutics Announces First Quarter 2018 Financial Results and Recent Corporate Developments
Sarepta Therapeutics Announces First Quarter 2018 Financial Results and Recent Corporate Developments
CAMBRIDGE, Mass.
Back U.S. FDA Approves Portola Pharmaceuticals’ Andexxa®, First and Only Antidote for the Reversal of Factor Xa Inhibitors
Back U.S. FDA Approves Portola Pharmaceuticals’ Andexxa®, First and Only Antidote for the Reversal of Factor Xa Inhibitors
SOUTH SAN FRANCISCO, Calif.
Celgene Reports First Quarter 2018 Operating and Financial Results
Celgene Reports First Quarter 2018 Operating and Financial Results
SUMMIT, N.
After FDA rebuff, Celgene on track to refile ozanimod — in 2019
After FDA rebuff, Celgene on track to refile ozanimod — in 2019
Celgene suffered an embarrassing setback in February when it got a refuse-to-file letter for its multiple sclerosis drug ozanimod.
FDA hits Mexican drugmaker Degasa with warning letter
FDA hits Mexican drugmaker Degasa with warning letter
The FDA issued a warning letter to Mexican finished-pharmaceutical manufacturer Degasa for issues including misbranding, failing to conduct adequate testing and problems with its water system.
Teva reports jump in first-quarter earnings, raises guidance
Teva reports jump in first-quarter earnings, raises guidance
AP — Israeli generic drug maker Teva Pharmaceutical Industries on Thursday said first-quarter earnings surged over 80 percent and raised its outlook for the rest of the year, citing progress in an a...
BeneVir to be bought by Janssen for up to $1.04 billion
BeneVir to be bought by Janssen for up to $1.04 billion
Privately-held USA-based biotech BeneVir has entered into a definitive agreement to be acquired by Janssen Biotech, part of US healthcare giant Johnson & Johnson (NYSE.
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