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Teva Outbids Valeant for Cephalon in $6.8B Cash Offer
for $6.6 billion, but is only the second largest deal of 2011, after Sanofi-aventis's takeover of Genzyme Corp. (See BioWorld Today, Sept. 29, 2009, and Feb. 18, 2011.) Published: May 3, 2011By Catherine Shaffer | Bio Perspectives | Tuesday, May 3, 2011 -
Biotech Ready to Strike Up a Conversation on Dealmaking
Paris-based Sanofi-Aventis SA's buyout of Genzyme includes by far the biggest CVR dollars this year – about $3.8 billion, most of that hinging on the success of multiple sclerosis drug alemtuzumabBy Jennifer Boggs | BioWorld Today | Tuesday, May 3, 2011 -
Teva Outbids Valeant for Cephalon in $6.8B Cash Offer
for $6.6 billion, but is only the second largest deal of 2011, after Sanofi-aventis's takeover of Genzyme Corp. (See BioWorld Today, Sept. 29, 2009, and Feb. 18, 2011.)By Catherine Shaffer | BioWorld Today | Tuesday, May 3, 2011 -
Other News To Note
entered into a research agreement with Sanofi Pasteur, of Lyon, France, the vaccines division of Sanofi-Aventis Group, and EnGen Bio Inc., of Redwood City, CalifBioWorld Today | Tuesday, May 3, 2011 -
Biotech Mergers And Acquisitions: Dec. 1, 2010 – Apr. 28, 2011#
Sanofi-Aventis SA (Paris) 8/31 4/11 $21.2B Sanofi-Aventis bought Genzyme for $21.2B Kinaxo Biotechnologies GmbH (Munich, Germany) Evotec AG (Hamburg, Germany) 2/10 4/19 €12 ($16.4) Evotec acquired all shares of Kinaxo with cash and 2.6M shares, plus a future milestone payment Neuro-Biotech Corp. (Basel, Switzerland) Auric Pharma Science (Madrid, Spain) 2/11 4/5 ND Neuro-Biotech received an unsolicited offer to purchase all outstanding shares at 15 cents per shareBioWorld Insight | Monday, May 2, 2011 -
Regeneron's ZALTRAP a Surprise Hit in Phase III
Regeneron and partner Sanofi-Aventis will waste no time preparing marketing approval applications for the FDA and European Medicines Agency for submission in the second half of 2011By Catherine Shaffer | BioWorld Today | Thursday, April 28, 2011 -
Karo Bio Shares Climb on Alkem Laboratories Deal
Earlier this month, Genzyme Corp., now a subsidiary of Paris-based Sanofi-Aventis Group, reported positive Phase III data for the antisense oligonucleotide, mipomersen, in HeFHBy Cormac Sheridan | BioWorld International | Wednesday, April 27, 2011 -
Sequella Inks $50M Licensing Deal for Tuberculosis Drug
Ltd., Johnson & Johnson, Pfizer Inc., GlaxoSmithKline plc, AstraZeneca plc and Sanofi-Aventis GroupBy Catherine Shaffer | BioWorld Today | Tuesday, April 26, 2011 -
$61.8M+ NovaMed Acquisition Strengthens SciClone in China
The current SciClone and NovaMed sales organizations in China will continue to operate separately under NovaMed CEO and co-founder Mark Lotter, who since helping start the company in August 2005 to provide "one-stop service" for companies looking to penetrate the China market, established exclusive licensing and promotion agreements with companies like Sanofi-aventis, Pfizer IncBy Tom Wall | Bio Perspectives | Wednesday, April 20, 2011 -
Other News To Note
Zealand Pharma A/S, of Copenhagen, Denmark, and Sanofi-Aventis S/A, of Paris, reported top-line results from the GetGoal-S Phase III trial of lixisenatide in Type II diabetes showing the drug achieved its primary efficacy endpoint of significant HbA1c reduction, improving glycemic control from baseline as compared to placebo, and causing a reduction in body weightBioWorld International | Wednesday, April 20, 2011 -
$61.8M+ NovaMed Acquisition Strengthens SciClone in China
The current SciClone and NovaMed sales organizations in China will continue to operate separately under NovaMed CEO and co-founder Mark Lotter, who since helping start the company in August 2005 to provide "one-stop service" for companies looking to penetrate the China market, established exclusive licensing and promotion agreements with companies like Sanofi-aventis, Pfizer IncBy Tom Wall | BioWorld Today | Wednesday, April 20, 2011 -
Phase III Clinical Trials Update: March 2011
Sanofi-Aventis SA (Paris) VEGF-Trap Aflibercept Non-small-cell lung cancer Failed to improve overall survival in a Phase III trial (3/14) Stemline Therapeutics Inc. (New York) SL-401 A cancer stem cell-targeting agent Acute myeloid leukemia FDA granted orphan drug designation (3/10) CARDIOVASCULAR United Therapeutics Corp. (Silver Spring, Md.) UT-15C Sustained-release oral formulation of treprostinil diethanolamine Pulmonary arterial hypertension Completed enrollmentBioWorld Insight | Monday, April 18, 2011 -
Academia-Fueled R&D Helps Gilead's Move into Oncology
Paris-based Sanofi-Aventis SA has joined forces with Harvard University on a research collaboration in areas such as cancer, diabetes and inflammation, and recently signed a new deal with Columbia University focused on diabetesBy Jennifer Boggs | BioWorld Insight | Monday, April 18, 2011 -
'Surprise' Bydureon Thumbs Up in Europe; Amylin Shares Rise
That program is partnered with Paris-based Sanofi-Aventis SABy Jennifer Boggs | BioWorld Today | Monday, April 18, 2011 -
Merrimack Pharmaceuticals' Series G Brings in $77M
Sanofi-Aventis pledged $60 million up front, with a potential $470 million in milestones...In July 2010, Merrimack and Sanofi-Aventis dosed the first patient in a Phase II study of MM-121 with Aromasin (exemestane) in breast cancerBy Catherine Shaffer | BioWorld Today | Monday, April 18, 2011 -
Clinic Roundup
Genzyme Corp., of Cambridge, Mass., a subsidiary of Sanofi-Aventis Group, reported additional five-year data from its Phase II multiple sclerosis trial showing that nearly two-thirds of alemtuzumab-treated patients remained free of clinically active disease as much as four years after most patients received their last course of treatmentBioWorld Today | Friday, April 15, 2011 -
Pieris, Daiichi Sankyo Ink Anticalins Deal for up to $296M
Ltd., of Osaka, Japan, and with Paris-based Sanofi Aventis Group and its vaccines arm Sanofi PasteurBy Cormac Sheridan | BioWorld International | Wednesday, April 13, 2011 -
Clinic Roundup
Zealand Pharma A/S, of Copenhagen, and Sanofi-Aventis S/A, of Paris, reported top-line results from the GetGoal-S Phase III trial of lixisenatide in Type II diabetes showing the drug achieved its primary efficacy endpoint of significant HbA1c reduction, improving glycemic control from baseline as compared to placebo, and causing a reduction in body weightBioWorld Today | Wednesday, April 13, 2011 -
Pieris, Daiichi Sankyo Ink Anticalins Deal for up to $296M
Ltd., of Osaka, Japan, and with Paris-based Sanofi Aventis Group and its vaccines arm Sanofi PasteurBy Cormac Sheridan | BioWorld Today | Wednesday, April 13, 2011 -
Pieris, Daiichi Sankyo Ink Anticalins Deal for up to $296M
Ltd., of Osaka, Japan, and with Paris-based Sanofi Aventis Group and its vaccines arm Sanofi PasteurBy Cormac Sheridan | Bio Perspectives | Tuesday, April 12, 2011
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