IRLAB receives MHRA approval to conduct Phase II trials with IRL790 in Britain
IRLAB has received approval from the Medicines & Healthcare products Regulatory Agency (MHRA) to conduct a Phase II study with the drug candidate IRL790 for treatment of L-dopa induced dyskinesias (LIDs). The study will be conducted at UK clinics.This Phase II clinical trial aims to study effect of IRL790 on dyskinesia in patients suffering from LIDs using UDysRS (the Unified Dyskinesia Rating Scale), the scale accepted by regulatory bodies. The 74 patients study will be conducted at several UK centres and is expected to be concluded in Q3 2018. The Phase II study is based on, and aims