Overview
ZD6474 Phase IIa Dose Finding Multicentre Study
Status:
Completed
Completed
Trial end date:
2007-01-01
2007-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To assess the objective response rates (by RECIST) to ZD6474 100, 200 and 300 mg/day respectivelyPhase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Genzyme, a Sanofi Company
Criteria
Inclusion Criteria:- Provision of written informed consent.
- Life expectancy of 12 weeks or longer.
Exclusion Criteria:
- Pregnancy, breast feeding or female patients wishing to become pregnant.
- Treatment with a non-approved or investigational drug within 30 days before enrolment