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Home » Newsletters » BioWorld

BioWorld

Dec. 20, 2011

View Archived Issues

Metamark, Janssen Biotech Ink Potential $365M Deal

Privately held Metamark Genetics Inc. landed a big fish, inking a research, collaboration and license agreement with Johnson & Johnson subsidiary Janssen Biotech Inc. potentially worth $365 million. Read More

Trius Antibiotic Tedizolid Hits Phase III Endpoints vs. Zyvox

Trius Therapeutics Inc. hit all primary and secondary endpoints in its first Phase III trial of antibiotic tedizolid (formerly torezolid), yet investors rewarded the San Diego biotech by pushing its shares down 12 percent. Read More

Alkermes Looks to Take on Abilify with Monthly Injectable

Advancing its third molecule to treat schizophrenia into a Phase III trial, Alkermes plc is zeroing in on the $4 billion Abilify market. Read More

Sygnis Shares Plunge on AX200 Acute Ischemic Stroke Miss

Shares in Sygnis Pharma AG plunged more than 62 percent Friday on news that its lead drug AX200 failed to demonstrate efficacy in a 328-patient Phase IIb trial in acute ischemic stroke. Read More

Other News To Note

• The ALS Therapy Development Institute entered a research agreement with Biogen Idec Inc., of Cambridge, Mass., and UCB Pharma SA, of Brussels, Belgium, to investigate the use of an anti-CD40L antibody as a potential therapy for amyotrophic lateral sclerosis (ALS). Read More

Financings Roundup

• Medicago Inc., of Quebec City, closed the second tranche of a C$22.5 million (US$21.8 million) private placement by Philip Morris Investments BV, consisting of 17.2 million common shares at C65 cents per share for gross proceeds of C$11.2 million. The first tranche, which closed in October, was a similar size. The proceeds will be used to advance Medicago's pandemic and seasonal influenza vaccine candidates. Philip Morris' investment stems from a rights agreement between the companies executed in 2008. Read More

Stock Movers

Read More

Clinic Roundup

• Isis Pharmaceuticals Inc., of Carlsbad, Calif., initiated a Phase I study of ISIS-SMNRx in patients with spinal muscular atrophy (SMA). The single-dose, dose-escalation study is designed to assess the safety, tolerability and pharmacokinetic profile of the drug in children with SMA between the ages of 2 and 14 who are medically stable. ISIS-SMNRx will be administered intrathecally as a single injection directly into the spinal fluid. Read More

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