NEW YORK--(BUSINESS WIRE)--
Levi & Korsinsky announces it has commenced an investigation of Argos Therapeutics, Inc. (ARGS). On February 17, 2017, Momenta announced that a contracted Pfizer facility used to manufacture the Company's Glatopa product had received a warning letter from the U.S. Food and Drug Administration. The Company’s Abbreviated New Drug Application (ANDA) for its Glatopa 40 mg product candidate is still under regulatory review, with final approval reliant upon the acceptable resolution of the compliance observations at the Pfizer manufacturing facility. In an earnings call on February 21, 2017, Momenta President and CEO Craig Wheeler stated that, as a result of the warning letter, “it is unlikely that Sandoz’s ANDA for Glatopa 40 mg will be approved in the first quarter of 2017.” To obtain additional information, go to:
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