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GLP Analogs for Diabetes in Wolfram Syndrome Patients
Lead sponsor
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
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
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 endpointbeta 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
- The Journal of clinical endocrinology and metabolism2016 Oct (month)PMID27459537doi:10.1210/jc.2016-2240via clinicaltrials gov reference derived + pubmed nct search
Provenance
Sources
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.