A Phase I study of AZD1480 in Patients with Advanced Solid Malignancies and Advanced Hepatocellular Carcinoma in the escalation phase,Non-Small Cell Lung Cancer(NSCLC) and non-smokers with lung metastasis and gastric cancer and solid tumour in the expansion phase.

Study identifier:D1060C00004

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Terminated/Withdrawn

Official Title

A Phase I, Open-label, Multicentre, Dose Escalation Study to Assess the Safety and Tolerability, and Pharmacokinetics of AZD1480 in Asian Patients with Advanced Solid Malignancies and Asian Patients with Child-Pugh A to B7 Advanced Hepatocellular Carcinoma (HCC) in the escalation phase, estimated glomerular filtration rate(EGFR) or ROS mutant NSCLC and non-smokers with lung metastasis and gastric cancer and solid tumour with biopsy available in the expansion phase.

Medical condition

solid tumour

Phase

Phase 1

Healthy volunteers

No

Study drug

AZD1480 Daily, AZD1480 BID

Sex

All

Actual Enrollment

47

Study type

Interventional

Age

18 Years - 150 Years

Date

Study Start Date: 01 Nov 2010
Primary Completion Date: 01 Dec 2012
Study Completion Date: 01 Dec 2012

Study design

Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment

Verification:

Verified 01 Jan 2014 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria