Viewing Study NCT02282267


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Study NCT ID: NCT02282267
Status: UNKNOWN
Last Update Posted: 2017-02-24
First Post: 2014-10-31
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Blood Detection of EGFR Mutation For Iressa Treatment
Sponsor: Peking University Cancer Hospital & Institute
Organization:

Study Overview

Official Title: Blood Detection of EGFR Mutation For Iressa Treatment
Status: UNKNOWN
Status Verified Date: 2017-02
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: Benefit
Brief Summary: This study was proposed to validate the efficacy of gefitinib as first-line therapy in advanced lung adenocarcinoma with EGFR mutation determined by plasma cf-DNA.
Detailed Description: Patients without enough tissue for EGFR mutation detection can also have opportunity to use EGFR-TKI as first line therapy. Meanwhile, this study was also proposed to explore the best intervention time of anti-resistant drugs (such as AZD 9291, a T790M inhibitor) through the quantitative and dynamic analysis of EGFR sensitive and resistant mutation in plasma cf-DNA during EGFR-TKI treatment process.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: