Study identifier:D1532C00016
ClinicalTrials.gov identifier:NCT00890825
EudraCT identifier:N/A
CTIS identifier:N/A
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
Non Small Cell Lung Cancer
Phase 2
No
AZD6244, docetaxel, Placebo
All
88
Interventional
18 Years - 130 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 May 2018 by AstraZeneca
AstraZeneca
-
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.
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).
Location
Location
Leuven, Belgium, 3000
Location
Liège, Belgium, 4000
Location
Charleroi, Belgium, 6000
Location
Liege, Belgium, B-4000
Location
Edegem, Belgium, 2650
Location
Brussels, Belgium, 1090
Location
Sofia, Bulgaria, 1756
Location
Varna, Bulgaria, 9010
Arms | Assigned Interventions |
---|---|
Active Comparator: AZD6244 + Docetaxel AZD6244 75 mg bd + Docetaxel 75 mg/m^2 | Drug: AZD6244 oral capsules, 75mg twice daily Other Name: Selumetinib Drug: docetaxel 75mg/m2 iv on day 1 of every 21 day cycle Other Name: Taxotere |
Placebo Comparator: Placebo + Docetaxel Placebo + Docetaxel 75 mg/m^2 | Drug: docetaxel 75mg/m2 iv on day 1 of every 21 day cycle Other Name: Taxotere Drug: Placebo placebo Other Name: Placebo |
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