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Symbollon gets U.S. FDA regulatory guidance for developing upper respiratory tract drug

Published in Respiratory Therapeutics Week, September 4th, 2006

Symbollon Pharmaceuticals, Inc. (SYMBA) announced it has received regulatory guidance concerning the appropriate preclinical steps necessary to initiate human clinical trials for its new drug, nasodine.

After discussions with the U.S. Food and Drug Administration (FDA), the company is planning to conduct a 30-day repeat dose animal study prior to filing an investigational new drug (IND) application in 2007.

Nasodine is a proprietary formulation designed to eliminate drug-resistant Staphylococcus aureus in the nasal cavity.

Part of Symbollon's business strategy is to develop a family of safe, broad-spectrum antimicrobial...

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