Findings demonstrated that single doses of MIV-711 were safe and well tolerated in healthy subjects and showed linear pharmacokinetics over the investigated dose range (20 – 600 mg). Further, serum levels of the bone resorption biomarker CTX-I were suppressed in a dose dependent manner with up to 79% reduction at 24 hours after dose.
Medivir's EVP Development Charlotte Edenius said that the compound is currently in a Phase Ib multiple ascending dose study for up to four weeks, which is expected to provide the company with additional information on the pharmacological effects on both bone and cartilage turnover.
Data were presented at the European Calcified Tissue Society (ECTS) Annual Meeting in Lisbon.
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