Trials / Completed
CompletedNCT00558103
Pazopanib Plus Lapatinib Compared To Lapatinib Alone In Subjects With Inflammatory Breast Cancer
A Randomized, Multicenter, Phase III Study Comparing the Combination of Pazopanib and Lapatinib Versus Lapatinib Monotherapy in Patients With ErbB2 Over-expressing Inflammatory Breast Cancer
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 163 (actual)
- Sponsor
- GlaxoSmithKline · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The double blind part of the study is being conducted to compare the efficacy and safety of pazopanib in combination with lapatinib with that of lapatinib alone in subjects with inflammatory breast cancer whose tumors overexpress the ErbB2 protein. There is also an Open-label pazopanib arm to this study designed to test whether pazopanib given alone and lapatinib given alone would be safe and effective to treat patients with inflammatory breast cancer.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | lapatinib | Oral administration |
| DRUG | Pazopanib | Oral administration |
Timeline
- Start date
- 2007-12-01
- Primary completion
- 2011-05-01
- Completion
- 2011-12-01
- First posted
- 2007-11-14
- Last updated
- 2013-02-04
- Results posted
- 2012-07-18
Locations
126 sites across 28 countries: United States, Australia, Belgium, Canada, Chile, China, Czechia, Egypt, France, Germany, Greece, Hong Kong, Israel, Italy, Morocco, Pakistan, Peru, Philippines, Romania, Russia, Singapore, South Korea, Spain, Taiwan, Thailand, Tunisia, Turkey (Türkiye), United Kingdom
Source: ClinicalTrials.gov record NCT00558103. Inclusion in this directory is not an endorsement.