Viewing Study NCT00481663



Ignite Creation Date: 2024-05-05 @ 5:34 PM
Last Modification Date: 2024-10-26 @ 9:33 AM
Study NCT ID: NCT00481663
Status: COMPLETED
Last Update Posted: 2017-04-04
First Post: 2007-06-01

Brief Title: A Study of Different Doses of Sitagliptin MK-0431 in Participants With Type 2 Diabetes Mellitus MK-0431-014
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: A Multicenter Double-Blind Randomized Placebo-Controlled Dose-Ranging Finding Study of Once-Daily Dosing of Sitaglipin MK-0431 in Patients With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control
Status: COMPLETED
Status Verified Date: 2017-03
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: A study of different doses of MK-0431 in participants with type 2 diabetes mellitus There have been 3 extensions to the base study Extension 1 up to Week 52 Extension 2 up to Week 106 and Extension 3 up to Week 158 The primary hypothesis for the study is that In participants with type 2 diabetes who have inadequate glycemic control after 12 weeks of treatment a dose-response will be seen across once-daily doses of MK-0431 in lowering hemoglobin A1C HbA1c
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
2007_570 None None None