An Open-Label, Non-Comparative, Phase III Study of the Raf-Kinase Inhibitor BAY 43-9006 as a Subsequent to First-Line Therapy in Patients With Advanced Renal Cell Carcinoma

Bayer

Status and phase

Completed

Phase 3

Conditions

Carcinoma, Renal Cell

Treatments

Drug: Nexavar (Sorafenib, BAY43-9006)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00492986

11941

2005-002524-34 (EudraCT Number)

Details and patient eligibility

About

Purpose of the study:

The purpose of this study is to make sorafenib available for patients with advanced Renal Cell Carcinoma, who have failed prior systemic therapy for advanced disease (i.e. requiring second line treatment), and who do not have access to or are not eligible for other clinical trials with sorafenib and who may benefit from treatment with sorafenib.

Patients will be treated orally with 400 mg bid sorafenib on a continuous basis and as a single agent. Patients may continue treatment until Disease Progression, intolerable toxicity, the patients chooses to withdraw consent or the patient is unlikely to benefit any further from treatment.

Overall, participation in the study will help determine the following:

Find out if patients receiving Sorafenib will live longer
Find out if Sorafenib helps to slow the worsening of kidney cancer
Find out if Sorafenib has an effect on the tumours

Enrollment

1,150 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The patient must provide written informed consent prior to receiving BAY 43-9006
The male or female patient must be at least 18 years of age
The patient must have advanced Renal Cell Carcinoma
The patient must have failed at least one prior systemic established therapy for advanced RCC (e. g. IL-2, IFN-a), or must have been unable to tolerate systemic therapy for advanced RCC, or is deemed by the Investigator to be unsuited for systemic therapy for advanced RCC
A patient, who has received prior systemic and local therapies, must have completely recovered from acute toxicity (i. e. resolved back to CTCAE Grade 1 or less, or is considered as not going to resolve), if any, prior to study entry
The patient must be, in the Investigator's opinion, reasonably likely to benefit from treatment with BAY 43-9006 as a single agent
The patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
The patient will not require other systemic anti-cancer chemotherapy, immunotherapy (including monoclonal antibodies) or hormonal therapy, except for bisphosphonates while taking BAY 43-9006
Both male and female patients must use adequate barrier birth control methods (oral contraceptives, injectable contraceptives, intrauterine devices, condoms, sterilization) during their participation in the protocol. The birth control methods must be used for 4 weeks for female patients and for 3 months for male patients after discontinuation of treatment with sorafenib
For patients, who have had major surgery, the wound must be completely healed prior to receiving BAY 43-9006 treatment (4 weeks)

Exclusion criteria

Patients who are currently enrolled in or have previously participated in any other sorafenib trial
Patients, who are eligible for or do have access to any other sorafenib clinical trial as to the knowledge of the Investigator
Patients who have a life expectancy of less than 2 months
Patients with metastatic brain or meningeal tumors
Patients are excluded who require any of the following:
Investigational drug therapy during the treatment with sorafenib or within 30 days prior to their first dose of sorafenib
Concomitant Rifampicin
Concomitant St. John's Wort (Hypericum perforatum) Warfarin is allowed; however, for patients receiving concomitant warfarin therapy close monitoring of Prothrombin Time (PT) should be performed (please note that no laboratory data are collected in this study)
Women who are pregnant or breast-feeding. Women of childbearing potential must have a negative pregnancy test performed within seven days of the start of study drug (please note that no laboratory data are collected in this study)
Patients with congestive heart failure greater than NYHA functional class II (symptomatic during ordinary activity)
Patients with cardiac arrhythmias greater than Grade 1 NCI CTCAE, Version 3.0 (conduction abnormality and supraventricular arrhythmia present but patient is asymptomatic; intervention not indicated, palpitations present and QTc > 0.45-0.47 second)
Patients with active coronary artery disease or ischemia
Patients with Child-Pugh class C hepatic impairment
Patients with severe renal impairment (calculated creatinine clearance of < 30 ml/min) or who require dialysis
Patients with active uncontrolled hypertension
Patients with recent or active bleeding diathesis
Patients with any medical condition which could jeopardize their safety while taking an investigational drug