Overview

Randomized Study of Sorafenib Dose Escalation in Patients With Previously Untreated Metastatic Renal Cell Carcinoma

Status:
Terminated
Trial end date:
2011-04-01
Target enrollment:
Participant gender:
Summary
The primary objective of this study is to compare the effectiveness of a dose-escalation regimen (400 to 800mg bid) relative to the standard dosing regimen (400mg bid) of sorafenib given in patients with metastatic RCC. The secondary objectives are to evaluate the effects of the dose-escalation regimen on the quality of life (QoL) of patients with metastatic RCC and to characterize the safety and tolerability profile of a dose-escalation regimen of sorafenib in patients with metastatic RCC.
Phase:
Phase 2
Details
Lead Sponsor:
Accelerated Community Oncology Research Network
Collaborator:
Bayer
Treatments:
Niacinamide
Sorafenib