Safety Study of TAK-559 in Treating Subjects With Type 2 Diabetes Mellitus

NCT00762112 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 316

Last updated 2012-11-12

No results posted yet for this study

Summary

The purpose of this study was to determine the long-term safety of TAK-559, once daily (QD), in subjects with Type 2 Diabetes.

Conditions

Interventions

DRUG

TAK-559

TAK-559 32 mg, tablets, orally, once daily for up to 24 months.

Sponsors & Collaborators

Principal Investigators

  • VP Biological Sciences · Takeda

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
25 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-11-30
Primary Completion
2004-12-31
Completion
2004-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00762112 on ClinicalTrials.gov