Phase
Condition
Diabetes And Hypertension
Diabetes Prevention
Diabetes Mellitus, Type 1
Treatment
Hyperglycemic clamp
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Men and women between the ages of 18 and 75 years old, inclusive, at the time ofscreening;
Females of non-childbearing potential must be ≥ 1 year post-menopausal or documentedas being surgically sterile. Females of childbearing potential must agree to use twomethods of contraception during the entire study;
Diagnosed with Type 1 diabetes >2-year duration based on clinical history or asdefined by the current American Diabetes Association (ADA) criteria;
Using hybrid closed loop, standard pump, or multiple daily injections;
Able to use a Continuous Glucose Monitoring (CGM) device;
A1c > 7% and ≤ 10%:
eGFR ≥ 60 mL/min/1.73m²;
BMI 18.5-35.0 kg/m2 ;
Able to provide written informed consent approved by an Institutional Review Board (IRB).
Exclusion
Exclusion Criteria:
History or evidence of clinically significant disorder or condition that, in theopinion of the Investigator, would pose a risk to subject safety or interfere withthe study evaluation, procedures, or completion;
History of pancreatitis, medullary thyroid carcinoma or liver disease:
Clinically significant diagnosis of anemia (Hemoglobin < 9 g/dl at screening);
Body Mass Index (BMI) < 18.5 kg/m2 and/or weight <50kg;
Body Mass Index (BMI) > 35 kg/m2;
Whole blood donation of 1 pint (500 mL) within 8 weeks prior to Screening. Donationsof plasma, packed RBCs, platelets or quantities less than 500 mL are allowed atinvestigator discretion;
Current or recent (within 1 month of screening) use of diabetes medications otherthan insulin; (examples include GLP-1, RA, SGLT-2i, Pramlintide, Metformin);
Women who are pregnant or lactating/breastfeeding;
Unable or unwilling to follow the study protocol or who are non-compliant withscreening appointments or study visits;
Any other condition(s) that might reduce the chance of obtaining study data, or thatmight cause safety concerns, or that might compromise the ability to give trulyinformed consent;
Severe hypoglycemic events or DKA within 3 months;
Currently using beta-blockers;
Adrenal insufficiency diagnosis.
Study Design
Study Description
Connect with a study center
University of California, San Diego - ACTRI
La Jolla, California 92037
United StatesSite Not Available

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