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AZD9291と新規治療薬の漸増投与との併用
基本情報
- NCT ID
- NCT02143466
- ステータス
- 実施中(募集終了)
- 試験のフェーズ
- 第1相
- 試験タイプ
- 介入
- 目標被験者数
- 344
- 治験依頼者名
- AstraZeneca
概要
The purpose of this study is to determine the safety, tolerability and preliminary anti-tumour activity of AZD9291 when given together with AZD6094 or selumetinib in patients with EGFR mutation positive advanced lung cancer
対象疾患
Advanced Non Small Cell Lung Cancer
介入
Part A - AZD9291 in combination with AZD6094(DRUG)
Part A - AZD9291 in combination with continuous selumetinib (Asian subjects)(DRUG)
Part A - AZD9291 in combination with continuous selumetinib (non-Asian subjects)(DRUG)
Part A - AZD9291 in combination with intermittent selumetinib(DRUG)
Part A - AZD9291 in combination with MEDI4736(DRUG)
Part B - AZD9291 in combination with AZD6094(DRUG)
Part B - AZD9291 in combination with selumetinib(DRUG)
Part B - AZD9291 in combination with MEDI4736(DRUG)
Part C - AZD6094 monotherapy (Japan only)(DRUG)
Part C - AZD9291 in combination with AZD6094 (Japan only)(DRUG)
Part D - AZD9291 in combination with AZD6094(DRUG)
依頼者(Sponsor)
アストラゼネカ株式会社(INDUSTRY)