Advanced Solid Malignancies Clinical Trial
Official title:
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
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.
n/a
Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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