A 3rd/4th Line Placebo-controlled Trial of Sorafenib in Patients With Predominantly Non Squamous Non-Small Cell Lung Cancer (NSCLC).

Completed · Phase 3 · Has a placebo group

Conditions studied: Carcinoma, Non-Small-Cell Lung

In brief

The purpose of the study is to see if sorafenib plus best supportive care (i.e. in addition to the non-cancer treatments patients would normally receive) is an effective treatment for lung cancer compared to best supportive care alone. The safety and tolerability of the two treatment groups will also be compared. The goal of the study is to test the ability of sorafenib to improve survival compared to best supportive care alone.

Key facts

Study ID

NCT00863746

Run by

Bayer

People needed

703

Starts

2009-04-01

Expected to finish

2013-04-01

Last updated by the study team

2015-01-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ability to understand and willingness to sign a written Informed Consent
• Advanced relapsed or refractory predominantly non squamous NSCLC. The diagnosis must have been confirmed cyto-/ histologically
• Patients must have measurable or non-measurable disease
• At least two but not more than three prior standard treatment regimens for NSCLC
• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1
• Male or female subjects >/= 18 years of age (>/=20 for Japan) at the time of Informed Consent
• Life expectancy of at least 12 weeks
• Ability to swallow oral medication
• Both men and women using adequate barrier birth control measures during the course of the trial and 4 weeks after the completion of trial
• Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to start of the study drug:
• Haemoglobin > 9.0 g/dl
• Absolute neutrophil count (ANC) >1,500/mm3
• Platelet count >/= 100,000/µl
• Total bilirubin </=1.5 x the upper limit of normal
• Alanine aminotransferase (ALT) < 2.5 x upper limit of normal (</= 5 x upper limit of normal in patients with liver metastases) Aspartate aminotransferase (AST) < 2.5 x upper limit of normal (</= 5 x upper limit of normal in patients with liver metastases)
• Alkaline phosphatase < 4 x upper limit of normal (</= 5 x upper limit of normal in patients with liver metastases)
• Prothrombin Time (PT)-International Normalized Ratio (INR) or Partial Thromboplastin Time (PTT) < 1.5 x upper limit of normal
• Serum creatinine < 1.5 x upper limit of normal
• Calculated creatinine clearance of >/= 50 mL/min

You may not qualify if…

• NSCLC patients with predominantly squamous cell carcinoma histology
• Excluded medical conditions:
• History of cardiac disease: Congestive heart failure, Active coronary artery disease (CAD), Cardiac arrhythmias (>Grade 2 NCI-CTCAE [National Cancer Institute-Common Terminology Criteria for Adverse Events] vers. 3.0)
• Uncontrolled hypertension despite two anti-hypertensive medications
• History of Human immunodeficiency virus (HIV) infection or chronic hepatitis B or C
• History of organ allograft
• Active clinically serious infections (> grade 2 NCI-CTCAE vers. 3.0)
• Patients with seizure disorder requiring medication
• Patients with evidence or history of bleeding diathesis or coagulopathy
• Patients undergoing renal dialysis
• Pulmonary hemorrhage/ bleeding event >/= CTCAE grade 2 within four weeks prior to the first dose of the study drug
• Any other hemorrhage/ bleeding event >/= CTCAE grade 3 within four weeks prior to the first dose of the study drug
• Thrombotic or embolic venous or arterial events such as cerebrovascular accident
• Pregnant or breast-feeding women.
• Any condition which could affect the absorption or pharmacokinetics of the study drug
• Prior treatment with other Vascular Endothelial Growth Factor (VEGF) (R) inhibitors, including compounds that impact vascularity (i.e. sunitinib, thalidomide, vandetanib, vascular disrupting agents [VDA], VEGF-trap and other experimental agents of this class). Only bevacizumab (Avastin) is permitted.

Where it is running

• Study site — Stanford, California, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Ramos Mejía, Buenos Aires, Argentina
• Study site — Buenos Aires, Ciudad Auton. de Buenos Aires, Argentina
• Study site — Córdoba, Córdoba Province, Argentina
• Study site — Córdoba, Córdoba Province, Argentina
• Study site — Rosario, Santa Fe Province, Argentina
• Study site — Rosario, Santa Fe Province, Argentina
• Study site — Santa Fe, Argentina
• Study site — Vienna, State of Vienna, Austria
• Study site — Graz, Austria
• Study site — Linz, Austria
• Study site — Antwerp, Belgium
• Study site — Bruxelles - Brussel, Belgium
• Study site — Charleroi, Belgium
• Study site — Genk, Belgium
• Study site — Brasília, Federal District, Brazil
• Study site — Belo Horizonte, Minas Gerais, Brazil
• Study site — Porto Alegre, Rio Grande do Sul, Brazil
• Study site — Porto Alegre, Rio Grande do Sul, Brazil
• Study site — Santo André, São Paulo, Brazil
• Study site — São José dos Campos, São Paulo, Brazil
• Study site — São Paulo, São Paulo, Brazil
• Study site — São Paulo, São Paulo, Brazil
• Study site — Fayetteville, Arkansas, United States

Full record on ClinicalTrials.gov

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