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BioWorld - Thursday, December 18, 2025
Home » Newsletters » BioWorld

BioWorld

Jan. 4, 2013

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Late-Round VC Financings Send 2012 Investments Up 13%

Whether it's Congress making decisions or venture capitalists making investments, leaving things to the last minute seems to be all the rage these days. Read More

Bacterial Immune System Used for Mammalian Genome Editing

Transcription activator-like effector nucleases, or TALENs, were named as one of the year's most exciting developments in Science magazine's 2012 list of top scientific advances, and 2013 began with another advance in the area of genome editing. Read More

Labrys Biologics Snags $31M Series A, CEO and Pfizer MAb

Labrys Biologics Inc. burst on the biotech scene with a $31 million Series A, a new president and CEO and the acquisition of a Phase II-ready anti-calcitonin gene-related peptide (CGRP) humanized monoclonal antibody (MAb) from Pfizer Inc. to treat chronic migraine. Read More

Financings Roundup

• Synageva BioPharma Corp., of Lexington, Mass., initiated an underwritten public offering of 1.7 million shares of common stock, seeking to raise up to $80 million. Read More

Other News To Note

• Icon Bioscience Inc., of Sunnyvale, Calif., said melphalan intraocular injection, its investigational product for treating retinoblastoma, was granted orphan designation by the FDA. Read More

Stock Movers

Read More

Clinic Roundup

• TheraVida Inc., of Mountain View, Calif., reported Phase II results showing that lead candidate Tolenix (THVD-201) produced statistically significant improvements in overactive bladder and urge urinary incontinence symptoms over placebo, and patients experienced efficacy similar in magnitude to the maximum dose of active control Detrol (2 mg tolterodine, administered twice daily). Read More

Pharma: Other News To Note

• Forest Laboratories Inc., of New York, said it entered a settlement agreement with Mumbai, India-based Glenmark Pharmaceuticals Ltd., and its affiliates, related to patent infringement litigation brought by Forest in response to Glenmark's abbreviated new drug application (ANDA) seeking to market generic versions of Forest's Bystolic (nebivolol) tablets. Read More

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