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Re: None

Wednesday, 02/05/2014 7:18:51 PM

Wednesday, February 05, 2014 7:18:51 PM

Post# of 6805
Won't be too long.....

--Provided U.S. Food and Drug Administration (FDA), on November 19, 2013,
with additional information requested in support of DARA's request for
orphan drug designation for the Company's Phase 2 development asset,
KRN5500, for the treatment of painful, treatment-refractory, chronic
chemotherapy-induced peripheral neuropathy ("CCIPN").