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A Multicenter Uncontrolled Study of Sorafenib in Patients With Unresectable and/or Metastatic Renal Cell Carcinoma

Phase 3
18 Years
Not Enrolling
Carcinoma, Renal Cell

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Trial Information

A Multicenter Uncontrolled Study of Sorafenib in Patients With Unresectable and/or Metastatic Renal Cell Carcinoma

Inclusion Criteria:

- Patients who have a life expectancy of at least 12 weeks

- Patients, who suffer from unresectable and/or metastatic, measurable RCC
histologically or cytologically documented. Patients with rare subtypes of RCC such
as pure papillary cell tumor, mixed tumor containing predominantly sarcomatoid cells,
Bellini carcinoma, medullary carcinoma, or chromophobe oncocytic tumors are excluded
from study participation.

- Patients who have received not more than one prior systemic therapy for advanced
disease which was completed at least 30 days prior to the first dose of study

- Patients who have at least one uni-dimensional measurable lesion by Computed
Tomography (CT)-scan or Magnetic Resonance Imaging (MRI) according to Response
Evaluation Criteria in Solid Tumours (RECIST)

- Patients with "Intermediate" or "low" risk per the Motzer score

- Patients who have an Eastern Co-operative Oncology Group (ECOG) performance status of
0 or 1

- Adequate bone marrow, liver and renal function at screening as assessed by the

- Total bilirubin < 1.5 x the upper limit of normal.

- Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) < 2.5 x upper
limit of normal (< 5 x upper limit of normal for patients with liver involvement of
their cancer).

- Amylase and lipase < 1.5 x the upper limit of normal.

- Serum creatinine < 2.0 x the upper limit of normal.

- Prothrombin Time (PT) or International Normalized Ratio (INR) and Partial
Thromboplastin Time (PTT) < 1.5 x upper limit of normal

Exclusion Criteria:

- Previous or concurrent cancer that is distinct in primary sit or histology from the
cancer being evaluated in this study EXCEPT cervical carcinoma in situ, adequately
treated basal cell carcinoma, superficial bladder tumors [Ta (Noninvasive papillary
carcinoma), Tis (Carcinoma in situ: "flat tumor") and T1 (Tumor invades subepithelial
connective tissue)] or any cancer curatively treated > 3 years prior to study entry)

- Patients who completed their prior systemic treatment regimen less than 30 days

- Cardiac arrhythmias requiring anti-arrhythmic (excluding beta blockers or digoxin),
symptomatic coronary artery disease or ischemia

- Active clinically serious bacterial or fungal infections

- Known history of human immunodeficiency virus (HIV) infection or chronic hepatitis B
or C requiring current interferon treatment

- Symptomatic metastatic brain or meningeal tumors unless the patient is > 6 months
from definitive therapy, has a negative imaging studies within 4 weeks of study entry
and is clinically stable with respect to the tumor at the time of study entry.

- Patients with evidence or history of bleeding diathesis.

- Patients with seizure disorder requiring medication

- History of organ allograft

- Substance abuse, medical, psychological or social conditions that may interfere with
the patient's participation in the study or evaluation of the study results

- Pregnant or breast-feeding patients.

Excluded concomitant medications:

- Concurrent anti-cancer chemotherapy, immunotherapy, or hormonal therapy except

- Radiotherapy during study or within 3 weeks of start of study drug.

- Biological response modifiers, such as Granulocyte-Colony Stimulating Factor (G-CFS)
or Granulocyte macrophage colony-stimulating factor (GM-CFS), within 3 weeks prior to
study entry or during study

- Significant surgery within 4 weeks prior to start of study drug

- Autologous bone marrow transplant or stem cell rescue within 4 months of study

- Investigational drug therapy during or within 4 weeks prior to first drug
administration and during the study

- St John's Wort

- Xiao Chai Hu Tang

- Prior and concomitant use of Bevacizumab, and all other drugs (investigational or
licensed) that target Vascular Endothelial Growth Factor (VEGF)/VEGF-Receptors,
Raf-kinase inhibitors (RKI), Methyl Ethyl Ketone (MEK) or Farnesyl transferase

Type of Study:


Study Design:

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Pharmacokinetics Measured as Area Under Curve (AUC[0-12h])

Outcome Description:

The AUC(0-12h) was the observed AUC, calculated using a combination of linear and log trapezoidal rules, from pre-dose to 12 hours post-dose. The normalized AUC (AUC norm) is AUC (0-12h) divided by (dose [mg]/weight [kg]).

Outcome Time Frame:

12 hours after at least 21 days of uninterrupted dosing

Safety Issue:


Principal Investigator

Bayer Study Director

Investigator Role:

Study Director

Investigator Affiliation:



China: Ministry of Health

Study ID:




Start Date:

December 2005

Completion Date:

May 2008

Related Keywords:

  • Carcinoma, Renal Cell
  • Sorafenib
  • Nexavar
  • Metastatic RCC
  • Renal Cell Carcinoma
  • Unresectable RCC
  • Carcinoma
  • Carcinoma, Renal Cell