A Multicenter Randomized Bioequivalence Study of a Novel Ready-to-Use Temozolomide Oral Suspension vs. Temozolomide Capsules
Background: Temozolomide (TMZ) oral suspension (Ped-TMZ, KIZFIZO<sup>®</sup>) is being developed for the treatment of relapsed or refractory neuroblastoma, a rare cancer affecting infants and young children. The study assessed the safety and the bioequivalence of this novel pediatric for...
Main Authors: | François Ducray, Carole Ramirez, Marie Robert, Maxime Fontanilles, Charlotte Bronnimann, Olivier Chinot, Florian Estrade, Xavier Durando, Stéphanie Cartalat, Jeremy Bastid, Hugues Bienayme, Caroline Lemarchand |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-11-01
|
Series: | Pharmaceutics |
Subjects: | |
Online Access: | https://www.mdpi.com/1999-4923/15/12/2664 |
Similar Items
-
Dispensing Oral Temozolomide in Children: Precision and Stability of a Novel and Ready to Use Liquid Formulation in Comparison with Capsule Derived Mixtures
by: Caroline Lemarchand, et al.
Published: (2023-11-01) -
Bioequivalence of Different Formulations of Zonisamide Oral Suspensions: A Short Review
by: Stević I, et al.
Published: (2023-11-01) -
Oseltamivir phosphate for suspension is bioequivalent to TAMIFLU in healthy volunteers: a randomized, open-label clinical study
by: Ying Wang, et al.
Published: (2023-02-01) -
Quinacrine enhances temozolomide cytotoxicity in temozolomide-sensitive and -resistant glioblastoma cells
by: Pingde Zhang, et al.
Published: (2018-01-01) -
Evaluation of Bioequivalence of Two Long-Acting 20% Oxytetracycline Formulations in Pigs
by: Jiyue Cao, et al.
Published: (2017-05-01)