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Friday, December 10, 2010
PharmAthene Inc., of Annapolis, Md., said the FDA lifted the partial clinical hold imposed last year on Valortim, a fully human anti-toxin monoclonal antibody being developed for the prevention and treatment of inhalational anthrax, clearing the company to move forward with a Phase I intravenous dose-escalation study in the coming weeks, which Roth Capital Partners analyst Joseph Pantginis called an "encouraging event" for the company.

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