Viewing Study NCT00122343



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00122343
Status: COMPLETED
Last Update Posted: 2015-02-19
First Post: 2005-07-21

Brief Title: AP23573 in Female Adult Patients With Recurrent or Persistent Endometrial Cancer 8669-019COMPLETED
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: A Phase II Study of AP23573 an mTOR Inhibitor in Female Adult Patients With Recurrent or Persistent Endometrial Cancer
Status: COMPLETED
Status Verified Date: 2015-02
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: This is an open-label nonrandomized multi-center study designed to evaluate the effect of AP23573 in patients with recurrent or persistent endometrial cancer The primary objective is to assess the efficacy of AP23573 in patients with recurrent or persistent endometrial cancer when administered once daily for 5 consecutive days QDx5 every two weeks at a dose of 125 mgday
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
AP23573-04-203 None None None