MONTREAL--(BUSINESS WIRE)--Mimetogen Pharmaceuticals Inc. (“Mimetogen”) today announced positive top line data from its second clinical study (Study Designation MIM-725) with MIM-D3, its lead drug for the treatment of dry eye syndrome. The trial demonstrated significant improvements in both signs and symptoms with 1% MIM-D3 versus placebo, together with excellent safety, comfort and tolerability profiles.
Mimetogen has completed its initial analysis of the data and met with the FDA in order to confirm the outstanding requirements for the remainder of the clinical development plan. “These clinical results further support the data generated in our first clinical trial (Study Designation MIM-724) and are promising for the use of MIM-D3 for the treatment of dry eye syndrome. Following our meeting with the FDA, we have begun preparations for the next clinical and non-clinical studies,” said Garth Cumberlidge, President and CEO of Mimetogen, adding: “MIM-D3, a novel growth factor mimetic, represents a potential first-in-class therapy for the estimated $3 billion US market.”
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