Viewing Study NCT02274740


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Study NCT ID: NCT02274740
Status: None
Last Update Posted: 2017-01-30 00:00:00
First Post: 2014-10-17 00:00:00
Is Possible Gene Therapy: False
Has Adverse Events: False

Brief Title: Effect of Lixisenatide on Postprandial Lipid Profile in Obese Type 2 Diabetic Patients
Sponsor: None
Organization:

Study Overview

Official Title: Effect of GLP-1 Receptors Agonist Lixisenatide on Postprandial Lipid Profile in Obese Type 2 Diabetic Patients
Status: None
Status Verified Date: 2017-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Sponsor decision not related to safety reasons
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Maximum study duration of approximately 2.5 months (study treatment) ± 2 days Day 0 (baseline) plus a 10-week open-label, active-controlled treatment period (Final/End-of-treatment Visit).
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?: