A Phase I, Open Label, Non-Randomised Study to Assess the Effect of Rifampicin on the Pharmacokinetics of Multiple Oral Doses of Cediranib (AZD2171, RECENTIN™), in Patients With Advanced Solid Tumours
Interventional
Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
To assess the steady-state PK parameters of cediranib in the presence and absence of rifampicin
PK assessments to be taken until Day 28. Days 7 and 14 PK parameters used to assess the primary variables.
No
Jane Robertson
Study Director
AstraZeneca, Alderley Park
Canada: Health Canada
D8480C00029
NCT00750841
September 2008
June 2013
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