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BioWorld - Wednesday, February 25, 2026
Home » Authors » Aaron Lorenzo

Articles by Aaron Lorenzo

Pozen's Stock Crushed On Trexima Approvable Letter

June 12, 2006
By Aaron Lorenzo
The FDA's request for more safety data on Pozen Inc.'s investigational migraine drug Trexima cut the company's stock value by 60 percent Friday. (BioWorld Today)
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Pozen's Stock Crushed On Trexima Approvable Letter

June 12, 2006
By Aaron Lorenzo
The FDA's request for more safety data on Pozen Inc.'s investigational migraine drug Trexima cut the company's stock value by 60 percent Friday. (BioWorld Today)
Read More

FDA Warns Against Use Of Unapproved Drug Products

June 9, 2006
By Aaron Lorenzo

FDA Warns Against Use Of Unapproved Drug Products

June 9, 2006
By Aaron Lorenzo

Galapagos Secures Deal With GSK On Osteoarthritis Program

June 8, 2006
By Aaron Lorenzo

HGS Signs Albuferon Deal With Novartis Worth Up To $550M

June 7, 2006
By Aaron Lorenzo
Human Genome Sciences Inc. could earn more than half a billion dollars per terms of a newly formed agreement with Novartis AG on Albuferon (albumin-interferon alpha 2b), a product expected to move into Phase III for chronic hepatitis C by the end of this year. (BioWorld Today)
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HGS Signs Albuferon Deal With Novartis Worth Up To $550M

June 7, 2006
By Aaron Lorenzo
Human Genome Sciences Inc. could earn more than half a billion dollars per terms of a newly formed agreement with Novartis AG on Albuferon (albumin-interferon alpha 2b), a product expected to move into Phase III for chronic hepatitis C by the end of this year. (BioWorld Today)
Read More

Myogen Starting Phase III For BP-Lowering Drug Darusentan

June 6, 2006
By Aaron Lorenzo

Tysabri Cleared; FDA Gives 'Very Rare' Second Approval

June 6, 2006
By Aaron Lorenzo
The FDA is allowing Tysabri to return to the market in a limited capacity for multiple sclerosis patients, three months after an advisory committee voted unanimously in favor of doing so. (BioWorld Today)
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Tysabri Cleared; FDA Gives 'Very Rare' Second Approval

June 6, 2006
By Aaron Lorenzo
The FDA is allowing Tysabri to return to the market in a limited capacity for multiple sclerosis patients, three months after an advisory committee voted unanimously in favor of doing so. (BioWorld Today)
Read More
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