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主に非扁平上皮非小細胞肺癌(NSCLC)患者を対象とした、ソラフェニブの第3/第4選択プラセボ対照試験。
基本情報
- NCT ID
- NCT00863746
- ステータス
- 完了
- 試験のフェーズ
- 第3相
- 試験タイプ
- 介入
- 目標被験者数
- 703
- 治験依頼者名
- Bayer
概要
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.
対象疾患
CarcinomaNon-Small-Cell Lung
介入
Sorafenib (Nexavar, BAY43-9006)(DRUG)
Placebo(DRUG)
依頼者(Sponsor)
バイエル薬品株式会社(INDUSTRY)