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[DOI] [PMC free article] [PubMed] [Google Scholar] 12.Tilg H., Moschen A.R

Part I tested single administration on day 1 as follows: three groups of postmenopausal females were randomized 6:2 to receive intravenous (IV) doses of co-administered anti-GDF8 6 mg/kg + anti-ActA 1, 3, or 10 mg/kg in sequence or placebo, in three 8-participant cohorts