CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 38 enrolled
Drug / intervention
AZD9291 tablets +4 moredrug
Likely dose
AZD9291 tablets 80mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02163733
NCT02163733Phase 1Completed

An Open-label, Randomised, Phase I, Study to Determine the Effect of Food on the Pharmacokinetics of Single Oral Doses of AZD9291 in Patients With EGFRm Positive NSCLC Whose Disease Has Progressed on an EGFR TKI

AstraZeneca·interventional·Posted Jun 16, 2014·Updated Jan 22, 2024

In Brief

A Phase 1 clinical trial evaluating AZD9291 tablets, Pharmacokinetic sampling - AZD9291, and 3 other interventions for Advanced Non Small Cell Lung Cancer and Advanced (Inoperable) Non Small Cell Lung Cancer. Completed, enrolled 38 participants across 13 sites in 4 countries.

Detailed Summary

This is a 2-part study in patients with epidermal growth factor receptor mutation positive (EGFRm+) non-small cell lung cancer (NSCLC) whose disease has progressed on treatment with an epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI): Part A will determine the effect of food on the pharmacokinetics (PK) of AZD9291; Part B will allow patients further access to AZD9291 and will provide for additional safety data collection. Part A is a randomised, open-label, 2 treatment period crossover study in which patients will each receive a single oral dose of AZD9291 (1 x 80 mg tablet) at breakfast time (approximately 0800) in each of 2 treatment periods (once immediately following a high fat meal \[fed\], and once in the fasted state \[fasted\]), with a washout period of 9 days between doses. Approximately 38 patients are planned to be enrolled and dosed; at least 30 evaluable patients will be required to complete Part A (ie, the last PK sample in Treatment Period 2 \[TP 2\] has been collected). Additional patients may be enrolled to allow for at least 30 evaluable patients

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, South Korea, Spain, United Kingdom
Collaborators--

Timeline

Phase 1CompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 16, 2014
Enrollment StartNov 14, 2014
Primary CompletionMar 24, 2015
Study CompletionJan 24, 2023
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 12.0 years ago

Interventions

AZD9291 tabletsdrug

AZD9291 tablets: Part A 80mg od, days 1 and 10 only. Part B 80mg od for 12 months.

Pharmacokinetic sampling - AZD9291procedure

Blood samples taken pre and post dosing of AZD9291 following either a period of fasting or consumption of a meal.

Dietary Fastedother

Fasted from 10 hours prior to dosing with 80mg AZD9291 tablet and 4 hours after dosing

Dietary High Fatother

Allocated breakfast prior to dosing with 80mg AZD9291 tablet

Pharmacokinetic sampling - AZ5140 and AZ7550procedure

Blood samples taken pre and post dosing of AZD9291 following either a period of fasting or consumption of a meal.