Ignite Creation Date:
2024-05-05 @ 11:29 AM
Last Modification Date:
2024-10-26 @ 9:08 AM
Study NCT ID:
NCT00057304
Status:
COMPLETED
Last Update Posted:
2023-04-28
First Post:
2003-03-31
Brief Title:
Study to Determine the Efficacy Safety Tolerability Pharmacokinetics of RO 205-2349 in Patients With Type 2 Diabetes Mellitus
Sponsor:
Hoffmann-La Roche
Organization:
Hoffmann-La Roche
Study Overview
Official Title:
A Phase II Randomized Double-Blind Dose-Ranging Study to Determine the Efficacy Safety Tolerability Pharmacokinetics of RO 205-2349 in Patients With Type 2 Diabetes Mellitus
Status:
COMPLETED
Status Verified Date:
2023-04
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:
The objective of the study is to determine the doses of Ro 205-2349 which when compared to placebo are efficacious safe and tolerable in improving glycemic control in patients with type 2 diabetes Doses of 2 to 5 mgday will be studied
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