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Delfa

← All trials/NCT01795144

CompletedPhase 1

Incretin Regulation of Insulin Secretion in Monogenic Diabetes

Asset

Avexitide

Listed sites

1

Recruiting sites

-

Actual enrollment

10

Study population

-

Eligibility highlights

Healthy volunteers

Primary endpoint

-

Registered trial locations

Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT01795144
Org study ID12-1517

Timeline

Milestones

Study first posted2013-02-20estimated
Last update posted2017-04-10actual
Study start2014-01 (month precision)
Primary completion2017-03actual (month precision)
Study completion2017-03actual (month precision)

Assets

Investigational agents

Who can enroll

Minimum age18 Years
Maximum age89 Years
SexAll
Healthy volunteersAccepted

Inclusion criteria

Monogenic Diabetes Subjects:

Inclusion Criteria:

Diagnosis of monogenic diabetes
Previously participated in US Neonatal Diabetes Registry (IRB 15617B) or Genetics of diabetes mellitus (IRB 6858)
Age: 18 years +

Exclusion criteria

Pregnancy
Acute medical illness or chronic conditions including: cardiac failure, renal insufficiency (estimated glomerular filtration rate <50 ml/min), hepatic insufficiency (known cirrhosis or hepatitis), chronic obstructive pulmonary disease, gastrointestinal disorders causing malabsorption, anemia (Hct < 36%), or uncontrolled hypertension

Healthy Controls:

Inclusion Criteria:

Good general health
Stable weight for 6 months
Age: 18 years +

Exclusion Criteria:

Pregnancy
Acute medical illness or chronic conditions including: cardiac failure, renal insufficiency (estimated glomerular filtration rate <50 ml/min), hepatic insufficiency (known cirrhosis or hepatitis), chronic obstructive pulmonary disease, gastrointestinal disorders causing malabsorption, anemia (Hct < 36%), or uncontrolled hypertension

Endpoints (0)

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.

No endpoints recorded for this trial.

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 6, 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 6, 2026 snapshot.