G-PLUS (GALLANT, GALLEX and ARMOR – Post treatment follow-up study)

Study identifier:D6160C00056

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Terminated/Withdrawn

Official Title

A Long-Term, Post-Treatment, Safety Follow-Up, Multi-Center Study in Patients with Type 2 Diabetes Mellitus from the GALLANT, GALLEX or ARMOR Studies.

Medical condition

Type 2 Diabetes

Phase

-

Healthy volunteers

No

Study drug

-

Sex

All

Actual Enrollment

4500

Study type

Observational

Age

18 Years +

Date

Study Start Date: 01 Sept 2005
Primary Completion Date: -
Study Completion Date: 01 Dec 2006

Study design

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

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria