InterMune, Roche receive OK for hepatitis trial
The phase Ia trial will assess safety, tolerability, pharmacokinetics and food affect in a single ascending dose study. InterMune expects to dose the first patient with ITMN-191 sometime
The European Medicines Agency (EMA) has validated the marketing authorisation application (MAA) from Pfizer and Valneva for their Lyme disease vaccine candidate, PF-07307405.