AZD2171
Drugoral tablet
Other names: cediranib, RECENTIN™
NCT Number: NCT00503477
A Phase I open label dose escalation study to assess the safety and tolerability of AZD2171 following single and multiple oral doses in patients in Japan with advanced solid malignancies. In addition there will be an expanded cohort multi-centre study phase with NSCLC patient and CRC patients
Looking for future studies?
Notify Me20 year–75 year
All sexes
Interventional
Phase 1
Research Site, Shizuoka, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
oral tablet
Other names: cediranib, RECENTIN™
Time frame: Assessed at each visit for 4 weeks
Time frame: Assessed at each visit for 4 weeks
Looking for future studies?
Notify MeAstraZeneca
Industry
A Phase I Open Label Dose Escalation Study for the Safety and Tolerability of AZD2171 Following Single and Multiple Oral Doses in Patients in Japan With Advanced Solid Malignancies
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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