A multicenter, open label, randomized, balanced, two treatment, three period, three sequence, reference replicate crossover, single dose, bioequivalence study of Capecitabine Tablets, USP 500mg manufactured by Amneal Pharmaceuticals, USA and XELODA® (Capecitabine) Tablets 500mg distributed by Genentech USA, Inc., A Member of the Roche Group, 1 DNA Way, South San Francisco, CA 94080-4990, following a single oral 2000mg (4x500mg) dose administration in adult human cancer patients under fed condition.
A Phase 3 Trial of IPX203 vs CD-LD IR in Parkinson’s Disease Patients with Motor Fluctuations (RISE-PD) (S16.010)
作者: LeWitt, Peter ; Stocchi, Fabrizio ; Ellenbogen, Aaron ; Espay, Alberto J. ; Isaacson, Stuart ; Hauser, Robert A. ; Pahwa, Rajesh ; D’Souza, Richard ; Visser, Hester
2022-05-03·Neurology
Duration of Benefit Per Dose: Post Hoc Analysis of “Good On” Time Per Dose for IPX203 vs CD-LD IR in the RISE-PD Phase 3 Trial (P10-11.002)
作者: Fisher, Stanley ; Fernandez, Hubert H. ; Banisadr, Ghazal ; Patel, Neepa ; Criswell, Susan ; Klos, Kevin ; Hauser, Robert A.