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Spots Global Cancer Trial Database for Phase II Single Arm Study of AZD9291 to Treat NSCLC Patients in Asia Pacific

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Trial Identification

Brief Title: Phase II Single Arm Study of AZD9291 to Treat NSCLC Patients in Asia Pacific

Official Title: A Phase II, Open Label, Single-arm Study to Assess the Safety and Efficacy of AZD9291 in Asia Pacific Patients With Locally Advanced/Metastatic Non-Small Cell Lung Cancer Whose Disease Has Progressed With Previous Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor Therapy and Whose Tumours Harbour a T790M Mutation Within the Epidermal Growth Factor Receptor Gene.

Study ID: NCT02442349

Interventions

AZD9291

Study Description

Brief Summary: A Phase II, Open Label, Single-arm Study to Assess the Safety and Efficacy of AZD9291 in Asia Pacific Patients with Locally Advanced/Metastatic Non-Small Cell Lung Cancer whose Disease has Progressed with Previous Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor Therapy and whose Tumours harbour a T790M mutation within the Epidermal Growth Factor Receptor Gene

Detailed Description: This is a phase II, open label, single arm study assessing the safety and efficacy of AZD9291 (80 mg, orally, once daily) in Asia Pacific patients with a confirmed diagnosis of Epidermal Growth Factor Receptor (EGFR) sensitising mutation positive (ie, G719X, exon 19 deletion, L858R, L861Q) and T790M mutation positive (hereafter referred to as EGFRm+ and T790M+) un-resectable, locally advanced or metastatic NSCLC (Stage IIIB-IV), who have progressed on an Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor(EGFR-TKI), either as first line treatment or following one line of EGFR-TKI and one line of platinum containing doublet chemotherapy. Patients must agree to provide a biopsy for central confirmation of T790M mutation status following confirmed disease progression on the most recent treatment regimen. The primary objective of the study is to assess the efficacy of AZD9291 by assessment of Objective Response Rate according to RECIST 1.1 by an Independent Central Review.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Kogarah, , Australia

Research Site, Nedlands, , Australia

Research Site, Woolloongabba, , Australia

Research Site, Beijing, , China

Research Site, Beijing, , China

Research Site, Beijing, , China

Research Site, Changchun, , China

Research Site, Chengdu, , China

Research Site, Chongqing, , China

Research Site, Chongqing, , China

Research Site, Fuzhou, , China

Research Site, Haikou, , China

Research Site, Hangzhou, , China

Research Site, Hangzhou, , China

Research Site, Hangzhou, , China

Research Site, Harbin, , China

Research Site, Jinan, , China

Research Site, Nanjing, , China

Research Site, Shanghai, , China

Research Site, Shanghai, , China

Research Site, Shanghai, , China

Research Site, Wuhan, , China

Research Site, Wuhan, , China

Research Site, Xi'an, , China

Research Site, Xi'an, , China

Research Site, Zhengzhou, , China

Research Site, Goyang-si, , Korea, Republic of

Research Site, Seongnam-si, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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