MLD granted second Pre-IND meeting with the FDA for PPI-1040 and treatment of RCDP

SASKATOON, SK, CANADA. MLD, a developer of advanced plasmalogen-based therapeutic products, is pleased to announce that it has been granted a second Type B pre-IND meeting with the FDA to discuss details surrounding the development of PPI-1040 for the treatment of RCDP. The meeting is scheduled for the last week in January, 2019, and focuses specifically on the proposed nonclinical development plan. "This meeting represents another step towards the ultimate goal of improving the lives of patients with RCDP," says Dr. Tara Smith, VP of Therapeutics, "and we are looking forward to the FDA's feedback on our proposed animal studies, and beginning the nonclinical safety and pharmacology program this coming year."


About MLD

MLD is a Canadian health prevention company developing novel plasmalogen replacement compounds for the treatment of various disorders associated with plasmalogen deficiency, including RCDP, Alzheimer's disease, Parkinson's disease, and Multiple Sclerosis, as well as companion screening tests that detect metabolic risk for chronic diseases including neurodegenerative disorders and cancer.

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Shawn Ritchie