Trials / Completed
CompletedNCT00305448
A Clinical Trial to Compare Efficacy and Tolerability of Fulvestrant 250mg, 250mg (Plus 250mg Loading Regimen) and 500mg
Phase II Study to Evaluate the Efficacy and Tolerability of Fulvestrant 250mg, 250mg (Plus 250mg Loading Regimen) and 500mg in Postmenopausal Women With ER +ve Advanced Breast Cancer Progressing or Relapsing After Previous Endocrine Therapy
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 143 (actual)
- Sponsor
- AstraZeneca · Industry
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This study will assess the relationship between fulvestrant dose and efficacy, and determine the dosing regimen as a second line therapy for Japanese postmenopausal women with oestrogen receptor positive advanced breast cancer.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Fulvestrant | 250 intramuscular injection |
| DRUG | Fulvestrant | 500 mg intramuscular injection |
Timeline
- Start date
- 2006-03-01
- Primary completion
- 2008-03-01
- Completion
- 2012-02-01
- First posted
- 2006-03-22
- Last updated
- 2012-02-15
- Results posted
- 2011-08-29
Locations
35 sites across 1 country: Japan
Source: ClinicalTrials.gov record NCT00305448. Inclusion in this directory is not an endorsement.