Status:

COMPLETED

Study to Investigate the Management of Hypertension and Efficacy of AZD2171 in Patients With Advanced Solid Tumours

Lead Sponsor:

AstraZeneca

Conditions:

Tumors

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

The purpose of this study is to determine whether doses of 30 mg and 45 mg AZD2171 can be well tolerated without significant drug withdrawal when accompanied by a suitable hypertension management stra...

Eligibility Criteria

Inclusion

  • Histological or cytological confirmation of advanced solid tumour, which is refractory to standard therapies or for which no standard therapy exists and for which there is a rationale for the therapeutic use of a vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor.

Exclusion

  • Prior treatment with a VEGF inhibitor
  • Poorly controlled hypertension

Key Trial Info

Start Date :

November 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2011

Estimated Enrollment :

119 Patients enrolled

Trial Details

Trial ID

NCT00264004

Start Date

November 1 2005

End Date

April 1 2011

Last Update

August 29 2012

Active Locations (6)

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Page 1 of 2 (6 locations)

1

Research Site

Freiburg im Breisgau, Germany

2

Research Site

Hamburg, Germany

3

Research Site

Amsterdam, Netherlands

4

Research Site

Nijmegen, Netherlands

Study to Investigate the Management of Hypertension and Efficacy of AZD2171 in Patients With Advanced Solid Tumours | DecenTrialz