NL-OMON46994已完成不适用
Phase I/II study with lapatinib plus trametinib in patients with metastatic KRAS mutant non-small cell lung cancer - Lapatinib plus trametinib in KRASm NSCLC
Antoni van Leeuwenhoek Ziekenhuis0 个研究点目标入组 132 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 132
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •1. Histological or cytological proof of metastatic NSCLC;
- •2. Written documentation of a known pathogenic KRAS (exon 2, 3 or 4) mutation and PIK3CA wild-type (exon 9 and 20).
- •3. Age * 18 years.
- •4. Able and willing to give written informed consent.
- •5. WHO performance status of 0 or 1 (part A and B)
- •6. Able to swallow and retain orally administered medications and does not have clinically significant gastrointestinal abnormalities that may alter absorption (e.g. malabsorption syndrome or major resection of the stomach or bowel)
- •7. Able and willing to undergo blood sampling for PK and PD analysis.
- •8. Able and willing to undergo a tumor biopsy prior to start, after two weeks on therapy and upon progression of disease
排除标准
- •1. Any treatment with investigational drugs within 30 days prior to receiving the first dose of investigational treatment.
- •2. History of another primary malignancy
- •3. Symptomatic or untreated leptomeningeal disease.
- •4. Symptomatic brain metastasis. Patients previously treated or untreated for these conditions that are asymptomatic in the absence of corticosteroid and anticonvulsant therapy (for at least 6 weeks) are allowed to enrol. Radiotherapy for brain metastasis must have been completed at least 6 weeks prior to start of study treatment. Brain metastasis must be stable with verification by imaging (e.g. brain MRI or CT completed at screening demonstrating no current evidence of progressive brain metastases). Patients are not permitted to receive anti-epileptic drugs or corticosteroids.
- •5. Patients previously treated with any targeted drug combination known to interfere with EGFR, HER-2, HER-3, HER-4 or MAPK- and PI3K-pathway components, including inhibitors of PI3K, AKT, mTOR, BRAF, MEK and ERK.
- •6. History of interstitial lung disease or pneumonitis
研究者
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