Post Marketing Surveillance Study of Byetta ™ (Exenatide) Use Among Filipino Patients

Study identifier:H80-PH-B006

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

Post Marketing Surveillance Study of Byetta ™ (Exenatide) Use Among Filipino Patients

Medical condition

Type 2 Diabetes Mellitus

Phase

-

Healthy volunteers

No

Study drug

-

Sex

All

Actual Enrollment

41

Study type

Observational

Age

18 Years +

Date

Study Start Date: 01 Feb 2008
Primary Completion Date: 01 Sept 2009
Study Completion Date: 01 Sept 2009

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Jan 2015 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

Eli Lilly and Company

Inclusion and exclusion criteria