Viewing Study NCT00328120



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00328120
Status: COMPLETED
Last Update Posted: 2010-11-17
First Post: 2006-05-18

Brief Title: Faslodex 500mg Multiple Dose Tolerability Study in BC Patients
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: An Open Multicentre Phase I Clinical Study to Assess the Tolerability of Fulvestrant 500 mg in Postmenopausal Women With Hormone Receptor Positive Advanced or Recurrent Breast Cancer
Status: COMPLETED
Status Verified Date: 2010-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary objective of this study is to assess the tolerability of 500mg fulvestrant in postmenopausal women with hormone receptor positive advanced or recurrent breast cancer
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
9238IL0062 None None None