← Trials/Trial dossier/NCT00154401

CompletedPhase 2

Effect of Liraglutide on Blood Glucose Control in Subjects With Type 2 Diabetes

Effect of Liraglutide on Glycaemic Control in Subjects With Type 2 Diabetes.

Lead sponsor

Novo Nordisk A/S

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

39

Recruiting sites

Enrollment

177

actual

Study population

Type 2 diabetes

Key I/E criterion

HbA1c ≤10%

Primary endpoint

HbA1c, change

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT00154401
Org study IDNN2211-1571

Timeline

Milestones

Study first posted2005-09-12estimated
Last update posted2017-01-25estimated
Study start2005-01 (month precision)
Primary completion2005-10actual (month precision)
Study completion2005-10actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Type 2 diabetes

Eligibility

Who can enroll

Minimum age18 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

Subjects diagnosed with type 2 diabetes mellitus and treated with either diet or single oral drug therapy
Diet treated subjects: 7.5% < HbA1c < 10%
Single oral drug therapy subjects: 7.0% < HbA1c < 9.5%
Body Mass Index (BMI): max 40 kg/m^2

Exclusion criteria

Subjects treated with thiazolidinediones or insulin
Subjects with any serious medical conditions

Endpoints (4)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Glycemic / diabetes
2
Weight & body composition
1
Safety / tolerability / PK
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Body weight after 14 weeks.

descriptive, improvement

Glycemic / diabetes

2 endpoints
Primary/protocol endpoint

HbA1c

Time frame:after 14 weeks treatment

HbA1c, change

change from baseline, improvement

LOINC 4548-4

Secondary/protocol endpoint

Glycaemic control parameters (fasting plasma glucose, glucose profiles) after 14 weeks.

Fasting glucose, change

change from baseline, improvement

LOINC 1558-6

Safety / tolerability / PK

1 endpoint
Secondary/protocol endpoint

Safety and tolerability

descriptive

Publications (5)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.