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Spots Global Cancer Trial Database for AZD6244 in Combination With Docetaxel Versus Docetaxel Alone in KRAS Mutation Positive NSCLC Patients

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Trial Identification

Brief Title: AZD6244 in Combination With Docetaxel Versus Docetaxel Alone in KRAS Mutation Positive NSCLC Patients

Official Title: Phase II, Double-Blind, Randomised, Placebo-Controlled Study to Assess the Efficacy of AZD6244 in Combination With Docetaxel, Compared With Docetaxel Alone, in 2nd Line Patients With KRAS Mutation Positive Locally Advanced Metastatic NSCLC

Study ID: NCT00890825

Study Description

Brief Summary: The purpose of this study is to compare the efficacy of AZD6244 in combination with docetaxel versus docetaxel alone in patients with KRAS mutation positive locally advanced or metastatic non small cell lung cancer.

Detailed Description: The primary objective of this study was to assess the efficacy in terms of overall survival (OS) of AZD6244 in combination with docetaxel, compared with docetaxel alone, in second-line patients with KRAS mutation-positive locally advanced or metastatic NSCLC. Amendment 4 of the CSP altered the primary objective and outcome variable from progression-free survival (PFS) to OS, and the secondary outcome variable changed from OS to PFS. The secondary objectives of the study were: * To further assess the efficacy of AZD6244 in combination with docetaxel, compared with docetaxel alone, in second-line patients with KRAS mutation-positive locally advanced or metastatic NSCLC * To assess the safety and tolerability profile of AZD6244 in combination with docetaxel * To investigate the use of plasma and serum as a potential source of circulating free tumour DNA (cfDNA) for the analysis of KRAS mutation status * To investigate the PK of AZD6244 and N-desmethyl AZD6244 and any other known metabolites when AZD6244 is administered in combination with docetaxel. The exploratory objectives of the study were: * To assess the prevalence, severity and change over time of advanced NSCLC cancer specific symptoms in patients receiving AZD6244 in combination with docetaxel and docetaxel alone * To explore potential biomarkers in residual tumour, plasma and/or serum taken for KRAS mutational analysis which may influence development of NSCLC (and associated clinical characteristics) and/or response (optional) * To investigate the relationship between AZD6244 and/or N-desmethyl AZD6244 and any other known metabolite plasma concentrations or exposure and clinical outcomes, efficacy, AEs, and/or safety parameters if deemed appropriate * To collect and store deoxyribonucleic acid (DNA), derived from a blood sample, for future exploratory research into genes that may influence response, eg, distribution, safety, tolerability, and efficacy of AZD6244 and/or agents used in combination and/or as comparators (optional).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Los Angeles, California, United States

Research Site, Aurora, Colorado, United States

Research Site, Boston, Massachusetts, United States

Research Site, Columbus, Ohio, United States

Research Site, Brussels, , Belgium

Research Site, Charleroi, , Belgium

Research Site, Edegem, , Belgium

Research Site, Leuven, , Belgium

Research Site, Liege, , Belgium

Research Site, Liège, , Belgium

Research Site, Belo Horizonte, , Brazil

Research Site, Ijuí, , Brazil

Research Site, Porto Alegre, , Brazil

Research Site, Rio de Janeiro, , Brazil

Research Site, Santo André, , Brazil

Research Site, Sao Paulo, , Brazil

Research Site, Sao Paulo, , Brazil

Research Site, Sao Paulo, , Brazil

Research Site, Plovdiv, , Bulgaria

Research Site, Sofia, , Bulgaria

Research Site, Sofia, , Bulgaria

Research Site, Sofia, , Bulgaria

Research Site, Sofia, , Bulgaria

Research Site, Varna, , Bulgaria

Research Site, Oshawa, Ontario, Canada

Research Site, Ottawa, Ontario, Canada

Research Site, Toronto, Ontario, Canada

Research Site, Ostrava, , Czechia

Research Site, Praha 8, , Czechia

Research Site, Znojmo, , Czechia

Research Site, Brest Cedex, , France

Research Site, Clermont Ferrand, , France

Research Site, Dijon, , France

Research Site, Lyon Cedex 08, , France

Research Site, Marseille, , France

Research Site, Rennes Cedex 9, , France

Research Site, Budapest, , Hungary

Research Site, Budapest, , Hungary

Research Site, Budapest, , Hungary

Research Site, Budapest, , Hungary

Research Site, Györ, , Hungary

Research Site, Mosdós, , Hungary

Research Site, Székesfehérvár, , Hungary

Research Site, Törökbálint, , Hungary

Research Site, Bologna, , Italy

Research Site, Genova, , Italy

Research Site, Milano, , Italy

Research Site, Orbassano, , Italy

Research Site, Perugia, , Italy

Research Site, Roma, , Italy

Research Site, Rozzano, , Italy

Research Site, Mexico, , Mexico

Research Site, Morelia, , Mexico

Research Site, Zacatecas, , Mexico

Research Site, Lima, , Peru

Research Site, Lima, , Peru

Research Site, Lima, , Peru

Research Site, Lima, , Peru

Research Site, A Coruña, , Spain

Research Site, Badalona(Barcelona), , Spain

Research Site, Barcelona, , Spain

Research Site, Madrid, , Spain

Research Site, Malaga, , Spain

Research Site, Málaga, , Spain

Contact Details

Name: Dr. Pasi Janne

Affiliation: Dana-Farber Cancer Institute, Boston, USA

Role: PRINCIPAL_INVESTIGATOR

Name: Dr. Gabriella Mariani

Affiliation: AstraZeneca, Hertfordshire, UK

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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