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GLP1-ex-vivo

TerminatedPhase NA

Quantitative GLP-1 Receptor Imaging Correlated to ex Vivo Distribution of In-111-exendin

Asset

Exenatide

GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

12

actual

Study population

Type 2 diabetes

Key I/E criterion

Primary endpoint

Correlation between the tracer uptake (counts) and beta cell mass (mg)

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 IDNCT03889496
Org study IDNL47132.091.14

Timeline

Milestones

Study start2015-11-16actual
Study first posted2019-03-26actual
Primary completion2021-06-14actual
Study completion2021-06-14actual
Last update posted2023-07-12actual

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

Scheduled for partial or complete pancreatectomy or Whipple procedure at Radboudumc

Exclusion criteria

Resection that provides insufficient amount of tissue
Previous treatment with synthetic Exendin (Exenatide, Byetta®) or Dipeptidyl- Peptidase IV inhibitors
Breast feeding
Pregnancy or the wish to become pregnant within 6 months
Renal disease
Liver disease
Age < 18 years

Endpoints (1)

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.

Other (unclassified)

1 endpoint
Primary/protocol endpoint/low confidence

Correlation between the tracer uptake (counts) and beta cell mass (mg)

Time frame:4 years

descriptive

Publications (1)

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.