The first clinical data with MIV-711, demonstrating it to be safe and tolerable at doses which potently decrease bone resorption biomarkers indicating that MIV-711 exerts the intended pharmacological effect on bone resorption. MIV-711 is currently being evaluated in a phase Ib multiple ascending dose study for up to 4 weeks. The top line data will be available around mid-year, while the full further phase I data will be presented at a scientific conference later this year, said Charlotte Edenius, EVP Development, Medivir AB.

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Medivir’s portfolio prioritize pharmaceuticals against infectious diseases caused by virus.
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Financial information 2013
  • The Interim Report for January-June will be published on 22 August
  • The Interim Report for January-September will be published on 21 November
Simeprevir presented via a webcast

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