Study identifier:D8480C00060
ClinicalTrials.gov identifier:NCT00981721
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, randomised, multi-centre, open-label study to determine the pharmacokinetics and tolerability of cediranib (RECENTIN™, AZD2171) following a single and multiple oral 20mg or 30 mg doses in Chinese patients with advanced solid malignancies
Advanced solid malignancies
Phase 1
No
cediranib (RECENTIN TM, AZD2171)
All
20
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 May 2025 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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This study is being carried out to see how single and multiple doses of cediranib are handled by the body (that is how they are absorbed, broken down and got rid of from the body) by measuring levels of drug in the blood in Chinese patients with advanced solid malignancies. The study will also assess the tolerability of 20 or 30 mg cediranib in Chinese patients and how the tumour responds to treatment with cediranib.
Location
Location
Beijing, Beijing, China
Location
Hong Kong, Hong Kong, China
Arms | Assigned Interventions |
---|---|
Experimental: 1 cediranib 20mg | Drug: cediranib (RECENTIN TM, AZD2171) 20 mg or 30mg cediranib once on Days 1, then 20 mg or 30mg cediranib once daily from Days 8 |
Experimental: 2 cediranib 30mg | Drug: cediranib (RECENTIN TM, AZD2171) 20 mg or 30mg cediranib once on Days 1, then 20 mg or 30mg cediranib once daily from Days 8 |
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