A Safety, Tolerability, and Efficacy Study of VC-02™ Combination Product in Subjects With Type 1 … (NCT03163511) | Clinical Trial Compass
CompletedPhase 1/2
A Safety, Tolerability, and Efficacy Study of VC-02â„¢ Combination Product in Subjects With Type 1 Diabetes Mellitus and Hypoglycemia Unawareness
United States49 participantsStarted 2017-07-06
Plain-language summary
VC02-101 will evaluate an experimental cell replacement therapy intended to provide a functional cure to subjects with Type 1 Diabetes and Hypoglycemia Unawareness.
Who can participate
Age range18 Years – 65 Years
SexALL
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Inclusion Criteria:
* Men and non-pregnant women
* Diagnosis of T1DM for a minimum of five (5) years
* Hypoglycemia unawareness or significant glycemic lability
* Stable diabetic treatment
* Willingness to use a continuous glucose meter
* Acceptable candidate for implantation
Exclusion Criteria:
* History of islet cell, kidney, and/or pancreas transplant.
* Six (6) or more severe, unexplained hypoglycemic events within six (6) months of enrollment
* Uncontrolled or untreated thyroid disease or adrenal insufficiency
* Diabetic complications such as severe kidney disease or renal dysfunction, proliferative retinopathy, diabetic foot ulcers, amputations attributable to diabetes, and/or severe peripheral neuropathy
* Non-compliance with current anti-diabetic regimen
* Detectable stimulated serum C-peptide during screening period assessment.
What they're measuring
1
Incidence of All AEs in Cohort 1 Participants
Timeframe: Enrollment (Visit 3, Day 1) through the Month 4 Visit