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Home » Newsletters » BioWorld

BioWorld

March 6, 2012

View Archived Issues

Aragon Moves Cancer Pipeline Forward with $42M Series C

Privately held Aragon Pharmaceuticals Inc. landed $42 million in an oversubscribed Series C financing to advance its pipeline of therapies targeting hormone-driven cancers, including ARN-509, the company's lead compound for the treatment of castration-resistant prostate cancer (CRPC). Read More

Shield Raises $13.9M, Gains Phase II Candidate from MRC

LONDON – Shield Therapeutics Ltd. signed an exclusive agreement with the UK Medical Research Council (MRC) for PT20, a treatment for hyperphosphatemia caused by kidney disease, and raised €10.5 million (US$13.9 million) for the onward development of the compound, which is ready for Phase II. Read More

Pediatrics Come up Short in Postmarket Requirements

WASHINGTON – Children are the ones most likely to pay the price when drugmakers delay their postmarket studies and trials. Read More

Start-Up NoNO Hopes to Get FDA's Yes for Stroke Drug

The statistics on stroke are enough to make the most hard-boiled drug developer cry. "Over a thousand treatments that have been developed in cells and in rodents have failed," Michael Tymianski told BioWorld Today. Read More

Other News To Note

• Arrowhead Research Corp., of Pasadena, Calif., and custom research organization Axolabs GmbH, of Kulmbach, Germany, inked an alliance and master services agreement for Axolabs to provide Arrowhead and its partners with first-in-class oligonucleotide optimization, synthesis and analysis for siRNA therapeutics. Read More

Stock Movers

Read More

Clinic Roundup

• Endocyte Inc., of West Lafayette, Ind., said the FDA approved its importation of a supply of Doxil (doxorubicin) from Europe for a Phase III trial (PROCEED). The trial began in May 2011, but the company stopped enrollment because of global shortages of Doxil. PROCEED compares EC145 in combination with Doxil to Doxil alone for ovarian cancer. Read More

Pharma: Clinic Roundup

• Teva Pharmaceuticals Ltd., of Jerusalem, reported findings from four Phase III trials showing that QNASL (beclomethasone dipropionate), a nasal aerosol corticosteroid, produced a significant change from baseline weekly averages of the subject-reported 24-hour reflective nasal symptom scores (rTNSS) over the first 30 weeks of treatment in patients with seasonal allergic rhinitis and perennial allergic rhinitis. Read More

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