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This is an open-label, Phase II, multi-center study evaluating DM199 in approximately 60 (sixty) Participants in two cohorts.
Cohort I: African Americans with CKD (Stage II or III), hypertension and non-diabetic Cohort II: Participants with IgA nephropathy diagnosis and CKD (Stage II or III)
Participants in each cohort will be enrolled in a parallel assignment to one of two doses:
Dose 1: DM199 2.0 µg/kg SC 2x week for 95 days Dose 2: DM199 5.0 µg/kg SC 2x week for 95 days
Not yet recruiting
DiaMedica Therapeutics Inc
Published on BioPortfolio: 2019-10-17T11:03:47-0400
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