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CompletedPhase 4

Effect of Repeated Administration of Liraglutide on Insulinogenic Indices

Asset

Liraglutide

Intravenous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

10

actual

Study population

Healthy volunteers

Key I/E criterion

Primary endpoint

The glucose-sensitivity of the beta cells

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 IDNCT02089256
Org study IDLI20/1101

Timeline

Milestones

Study first posted2014-03-17estimated
Last update posted2015-04-01estimated
Study start2014-06 (month precision)
Primary completion2015-03actual (month precision)
Study completion2015-03actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Healthy volunteers

Eligibility

Who can enroll

Minimum age18 Years
Maximum age50 Years
SexAll
Healthy volunteersAccepted

Inclusion criteria

Weight 50-100 kg

Exclusion criteria

Chronic disease
Concomitant drug use
Pregnancy or lactation
Fasting glucose >6 mmol/L.

Endpoints (2)

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
1
Other (unclassified)
1

Glycemic / diabetes

1 endpoint
Primary/protocol endpoint/low confidence

Change in the glucose-sensitivity of the beta cells

Time frame:baseline, first dose, after 3-weeks on treatment

change from baseline, improvement

Other (unclassified)

1 endpoint
Secondary/protocol endpoint/low confidence

Effects on adrenal hormones

Time frame:baseline, acute administration, 3 weeks

change from baseline, descriptive

Publications (3)

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.