LRRK2-IN-7 No Further a Mystery
All enrolled sufferers who been given at least just one dose of zosuquidar or placebo for the duration of induction were being monitored for the event of adverse gatherings (439 clients, 219 on zosuquidar and 210 on placebo). The commonest adverse events had been relevant to the duration of extended and sizeable myelosuppression as is expected with