Study identifier:D8480C00060
ClinicalTrials.gov identifier:N/A
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 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
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 |