Safety, tolerability and pharmacokinetics of regorafenib in pediatric subjects

Mise à jour : Il y a 4 ans
Référence : EUCTR2013-003579-36

Femme et Homme

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Extrait

- To define the safety profile, maximum tolerated dose (MTD) and recommended phase II dose (RP2D) of regorafenib administered orally as a single agent in a 3-weeks-on / 1- week-off schedule in repeating cycles of 28 days in pediatric subjects with solid malignant tumors recurrent or refractory to standard therapy. - To characterize the pharmacokinetics (PK) of regorafenib.


Critère d'inclusion

  • Pediatric patients with solid malignant tumors that are recurrent or refractory to standard therapy

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