Vicore Pharma receives regulatory approval to start phase II clinical trial with VP01 (C21) in patients with IPF
Gothenburg, May 5, 2020 – Vicore Pharma Holding AB (publ), a pharmaceutical company dedicated to developing innovative medicines for rare lung disorders, today announces the approval by the UK regulatory agency (MHRA[1]) of the clinical trial application (CTA) for a phase II study with its proprietary compound VP01 (C21) in patients with IPF (idiopathic pulmonary fibrosis).Approximately five weeks after submitting the CTA, Vicore Pharma has received approval from the MHRA to start the study. In addition to the MHRA approval, a favourable opinion from the ethics committee is also required