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Spots Global Cancer Trial Database for Phase II AZD9291 Open Label Study in NSCLC After Previous EGFR TKI Therapy in EGFR and T790M Mutation Positive Tumours

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Trial Identification

Brief Title: Phase II AZD9291 Open Label Study in NSCLC After Previous EGFR TKI Therapy in EGFR and T790M Mutation Positive Tumours

Official Title: Phase II, Open Label, Single-arm Study to Assess Safety and Efficacy of AZD9291 in Patients With Locally Advanced/Metastatic NSCLC Whose Disease Has Progressed With Previous EGFR TKI and Whose Tumours Are EGFR and T790M Mutation Positive

Study ID: NCT02094261

Interventions

AZD9291

Study Description

Brief Summary: A Phase II, Open Label, Single-arm Study to Assess the Safety and Efficacy of AZD9291 in 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 are Epidermal Growth Factor Receptor Mutation and T790M Mutation Positive

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 patients with a confirmed diagnosis of Epidermal Growth Factor Receptor mutation positive and T790M mutation positive NSCLC,who have progressed following prior therapy with an approved Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR-TKI) agent. 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, La Jolla, California, United States

Research Site, Orange, California, United States

Research Site, New Haven, Connecticut, United States

Research Site, Norwalk, Connecticut, United States

Research Site, Indianapolis, Indiana, United States

Research Site, Boston, Massachusetts, United States

Research Site, Lebanon, New Hampshire, United States

Research Site, New York, New York, United States

Research Site, Durham, North Carolina, United States

Research Site, Edmonton, Alberta, Canada

Research Site, Ottawa, Ontario, Canada

Research Site, Toronto, Ontario, Canada

Research Site, Hong Kong, , Hong Kong

Research Site, Shatin, , Hong Kong

Research Site, Milano, , Italy

Research Site, Milan, , Italy

Research Site, Napoli, , Italy

Research Site, Perugia, , Italy

Research Site, Verona, , Italy

Research Site, Akashi-shi, , Japan

Research Site, Chuo-ku, , Japan

Research Site, Kitaadachi-gun, , Japan

Research Site, Kitakyushu-shi, , Japan

Research Site, Koto-ku, , Japan

Research Site, Nagoya-shi, , Japan

Research Site, Nagoya-shi, , Japan

Research Site, Niigata-shi, , Japan

Research Site, Osaka-shi, , Japan

Research Site, Osaka-shi, , Japan

Research Site, Osakasayama, , Japan

Research Site, Sakai-shi, , Japan

Research Site, Wakayama-shi, , Japan

Research Site, Yokohama-shi, , Japan

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

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

Research Site, Seoul, , Korea, Republic of

Research Site, A Coruña, , Spain

Research Site, Barcelona, , Spain

Research Site, Madrid, , Spain

Research Site, Majadahonda, , Spain

Research Site, Málaga, , Spain

Research Site, Valencia, , Spain

Research Site, Taichung, , Taiwan

Research Site, Taipei, , Taiwan

Contact Details

Name: Glenwood Goss, MD

Affiliation: 501 Smyth Road, Ottawa, Canada

Role: PRINCIPAL_INVESTIGATOR

Name: Tetsuya Mitsudomi, MD

Affiliation: Kinki University Hospital, Faculty of Medicine, Osaka, Japan

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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