https://www.selleckchem.com/pr....oducts/i-bet-762.htm
All newly diagnosed APL patients were in MCR with a median follow-up of 28 months (range, 23 to 37 months). Both the estimated 3-year EFS and OS rates were 100%. The pharmacokinetics and safety oral AS S formula was evaluated for the first time in pediatric APL. The pharmacokinetic assessment demonstrated that the dosing regimen of 60 mg/kg/d TID resulted in a higher steady-state through concentration in children than that which was achieved in adults. The results of this study indicate that the AS S formula is safe in newly diagnosed
Curtir
Comentario
Compartilhar
