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Home » Newsletters » BioWorld

BioWorld

Sep. 10, 2012

View Archived Issues

Money Raised By Biotech: Jan. 1 - Aug. 31, 2012

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FDA Approvals In August

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Phase I Clinical Trials Update: August 2012

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Phase II Clinical Trials Update: August 2012

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Phase III Clinical Trials Update: August 2012

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Pharma Clinical & FDA Action Update: August 2012

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Non-U.S. Clinical Trials & Regulatory Actions: August 2012

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FDA Submissions, Approvals & Other Actions: August 2012

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DNA Switches Study Adds Utility to Existing GWAS Data

Last week's data deluge describing the most comprehensive map to date of regulatory elements in the human genome gave scientists new insights into how DNA that does not code for proteins functions within the genome. And that new understanding may enable them to get more information out of older genomewide association studies (GWAS). Read More

Idenix Tries to Convince FDA Not All Nucs Are Created Equal

The demise of Bristol-Myers Squibb Co.'s hepatitis C drug BMS-986094, which BMS discontinued development of after patients in its Phase IIb study experienced heart and kidney toxicity, stretched further than just the big pharma. The FDA put a partial clinical hold on Idenix Pharmaceuticals Inc.'s related nuc IDX184 and then slapped a hold on its next-generation nuc, IDX19368, as well. Read More

SEC Looks to Improve Access To Markets for Small Companies

There is plenty of evidence to suggest that small and emerging biotechnology companies could significantly benefit from modifications to the existing SEC rules and regulations affecting their access to the capital markets. Read More

Week in Review

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Word on the Street

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Week in Washington

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Stock Gainers and Losers For The Week

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BioWorld Stock Report For Public Biotechnology Companies

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