Evaluating Efficacy and Safety of Erlotinib Versus Gemcitabine Plus Cisplatin as Neoadjuvant Chemotherapy
- Sponsor
- Shanghai Chest Hospital
- Study ID
- NCT01297101
- Status
- Temporarily Not Available
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Erlotinib — DRUG150mg/qd, on day 15-28 of each 28 day cycle.
Study Details
The aim of this study is to investigate the efficacy and safety of Tarceva versus combination of Gemcitabine plus Cisplatin as neoadjuvant treatment in patients with stage IIIA-N1,N2 NSCLC with EGFR activating mutation in exon 19 or 21.
Key Dates
- First listed
- Feb 16, 2011
- Status verified
- Jan 2011
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