AP1189 can be dosed for three months in future clinical studies
SynAct Pharma AB ("SynAct") today announced that the company successfully has completed preclinical toxicology studies aimed to support 3 months dosing in future clinical trials with its lead candidate product, AP1189.No unforeseen observations were identified and importantly, the studies identified no-observed-adverse-effect levels (NOAEL) at the same or higher levels as identified in the four weeks preclinical toxicology studies conducted prior to initiation of the clinical development of the AP1189 compound. The preclinical studies have been conducted in accordance with international