Viewing Study NCT00062751



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00062751
Status: COMPLETED
Last Update Posted: 2011-04-15
First Post: 2003-06-12

Brief Title: Study Evaluating Temsirolimus CCI-779 In Breast Neoplasms
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: A Phase 2 Randomized Open-Label Study Of Letrozole In Combination With Two Dose Levels And Schedules Of Oral Temsirolimus CCI-779 Or Letrozole Alone In Postmenopausal Women With Locally Advanced Or Metastatic Breast Cancer
Status: COMPLETED
Status Verified Date: 2011-04
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: To evaluate the preliminary activity and pharmacokinetics of 2 separate doses and schedules of orally administered Temsirolimus CCI-779 given in combination with daily letrozole compared to letrozole alone in the treatment of locally advanced or metastatic breast cancer in postmenopausal women All patients must be appropriate to receive endocrine therapy as treatment for advanced disease
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
B1771005 None None None