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EMA confirms benefits of BI's Pradaxa but wants clearer guidance

The European Medicines Agency has recommended updating the product information for Boehringer…See More
18 hours ago
Michael Honatan posted a discussion

Osiris GvHD therapy is world's first approved stem cell drug

Osiris Therapeutics has been given the green light by regulators in Canada for Prochymal, its…See More
Monday
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Maria Burneo posted a discussion

Roche scraps cholesterol drug dalcetrapib after Phase III fail

Shares in Roche have taken a bashing after the Swiss major has pulled the plug on dalcetrapib, a…See More
May 8
 

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EMA confirms benefits of BI's Pradaxa but wants clearer guidance

Started by Pharmaceutical 18 hours ago. 0 Replies

The European Medicines Agency has recommended updating the product information for Boehringer Ingelheim's new blockbuster bloodthinner Pradaxa concerning the risk of bleeding but has again stressed the benefits of the drug.Noting that "bleeding is a…Continue

Tags: but, wants, clearer, guidance, Pradaxa

Osiris GvHD therapy is world's first approved stem cell drug

Started by Michael Honatan on Monday. 0 Replies

Osiris Therapeutics has been given the green light by regulators in Canada for Prochymal, its treatment for acute graft-versus host disease in children, making it the world’s first approved drug which has a stem cell as its active ingredient.The US…Continue

Tags: approved, stem, cell, drug, first

Roche scraps cholesterol drug dalcetrapib after Phase III fail

Started by Maria Burneo May 8. 0 Replies

Shares in Roche have taken a bashing after the Swiss major has pulled the plug on dalcetrapib, a drug which raises 'good' cholesterol, after suffering a late-stage study failure.On the basis of results from the second interim analysis of the…Continue

Tags: Phase, III, fail, after, dalcetrapib

Abbott acquires kidney drug from Action for $110 million

Started by Michael Honatan May 7. 0 Replies

Abbott Laboratories is shelling out $110 million to buy an investigational kidney drug from Denmark's Action Pharma.The treatment in question, AP214, is in development to prevent acute kidney injury (AKI) associated with major cardiac surgery in…Continue

Tags: for, $110, million, Action, from

Featured news

D-Day for Lipitor as scramble for US market share begins

Posted by Nicolás Mena on November 30, 2011 at 9:51pm 0 Comments

Lipitor, the world's best-selling drug, goes off-patent in the USA today, and observers are watching keenly to see how damaging the loss will be to Pfizer and how much generics firms will benefit.

Pfizer is fighting hard to keep hold of a…

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Novartis triple-combo blood pressure drug gets European OK

Posted by Elisa Marferson on November 28, 2011 at 11:55pm 0 Comments

Novartis has been given the green light to market its triple combination antihypertensive Rasitrio.

 

The European Commission has approved Rasitrio as a single pill for the treatment of high blood pressure. It combines the Swiss…

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Facebook in firing line over tale of two Mercks

Posted by Michael Honatan on November 24, 2011 at 8:56pm 0 Comments

Germany's Merck KGaA has asked a New York judge to force Facebook to provide information about "an apparent takeover" of its page on the social networking site, which is now occupied by information on rival Merck & Co.

Robert Horowitz…

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EU approves Pfizer's Vyndaqel, FDA backs Prevnar 13 expansion

Posted by Nicolás Mena on November 17, 2011 at 9:15pm 0 Comments

The European Commission has approved Pfizer's Vyndaqel for the treatment of a rare genetic disease.

Vyndaqel (tafamidis) has been given the green light for transthyretin familial amyloid polyneuropathy (TTR-FAP), a progressive and fatal…

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US CBO doubles estimated savings from pay-for-delay ban

Posted by Nicolás Mena on November 14, 2011 at 8:29pm 0 Comments

The US Congressional Budget Office (CBO) now estimates that banning "pay-for-delay" deals between brand-name and generic drugmakers would reduce the federal deficit by $4.8 billion over 10 years; last year it said the measure would cut…

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AstraZeneca/Targacept antidepressant fails Phase III study

Posted by Nicolás Mena on November 8, 2011 at 8:18pm 0 Comments

AstraZeneca and partner Targacept have announced disappointing top-line results from the first of four late-stage studies on their new antidepressant.

Specifically, the Renaissance 3 Phase III study investigated TC-5214 as an adjunct…

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