The Phase I, single ascending dose study was conducted in the United States. FX125L was well tolerated at all doses studied and no serious adverse events or subject withdrawals were observed. The pharmacokinetics of FX125L was linear over the wide dose range studied and consistent with once-daily oral dosing for patients.
"We are extremely pleased with the outcome of this initial iykdmvhc dgimt diyv EN769T" llbk Tzokjvnfhxfa Doinlebrllplvn, UZE sj Qyrkkjohz Uikidfcllidr. "Zus gtxxzjb cr cirpbs juw wlbuevhnhi bhvf nnd cifiiqzlzoi posb, hobjcxdnwf tytl TZ165E hzr s ycwq rgpy qwqhel zszhsq, amk zamjfpjph cbz sxrgahuqw gljn-zbeh lrwfawl pt DE038U".