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Study is Designed to Assess the Safety and Tolerability of AZD4547 at Increasing Doses in Patients With Advanced Tumours
Not Recruiting
Trial ID: NCT00979134
Purpose
This study is primarily designed to assess the safety and tolerability of AZD4547 at
increasing doses in patients with advanced solid malignancies and for whom no standard
medication options are available. It also assesses the blood levels and action of AZD4547 in
the body over a period of time.
Official Title
A Phase I, Open-Label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of Ascending Doses of AZD4547 in Patients With Advanced Solid Malignancies
Stanford Investigator(s)
Joel Neal, MD, PhD
Associate Professor of Medicine (Oncology)
Eligibility
Inclusion Criteria:
- Minimum life expectancy of 12 weeks
- The presence of a solid, malignant tumour that is resistance to standard therapies or
for which no standard therapies exist
- In the expansion for the study patients must have a tumour at least 1cm in size that
can be measure using a CT or MRI scan, and provide a tumour sample to the sponsor
company for testing of FGFR1 and/or 2 amplification
- Expansion, 5 groups of advanced cancer
- Solid tumours,FGFR1 and/or FGFR2 gene amplified
- Squamous NSCLC, FGFR1 gene low & high amplified
- Gastric adenocarcinoma, including the lower oesophagus/gastro-oesophageal junction,
FGFR2 gene low & high amplified
- Aged at least 25 years
Exclusion Criteria:
- Treatment with any other chemotherapy, immunotherapy or anticancer agents within 3
weeks before the first dose of study
- An inability to be able to take the study medication
- A bad reaction to AZD4547 or any drugs similar to it in structure or class.
Intervention(s):
drug: AZD4547
drug: AZD4547
drug: AZD4547
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Cancer Clinical Trials Office
650-498-7061