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WithdrawnPhase NA

GLP Analogs for Diabetes in Wolfram Syndrome Patients

Asset

Exenatide

GLP-1 agonist

Listed sites

0

Recruiting sites

Enrollment

actual

Study population

Wolfram Syndrome

Key I/E criterion

Primary endpoint

Beta cell function

Identifiers

Registered as

NCT IDNCT01302327
Org study IDwolfram-HMO-CTIL

Timeline

Milestones

Study first posted2011-02-24estimated
Study start2011-03-01
Primary completion2013-03-01estimated
Study completion2013-03-01actual
Last update posted2022-03-29actual

Assets

Investigational agents

Study populations

Who this study enrolls

Wolfram Syndrome

Eligibility

Who can enroll

Minimum age18 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

1. Genetic or definitive clinical diagnosis of Wolfram's syndrome including: diabetes mellitus, optic atrophy and at least one additional neurological dysfunction (diabetes insipidus, sensorineural deafness, neurogenic bladder or other type of autonomic or peripheral neuropathy)

2. Age >18 years

3. Duration of diabetes of <10 years.

Exclusion criteria

1. pregnant women

2. patients who are unable to give inform consent.

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.

Glycemic / diabetes

1 endpoint
Primary/protocol endpoint/low confidence

beta cell function

Time frame:3 months

change from baseline, improvement

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.