Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:13 PM
Ignite Modification Date:
2025-12-24 @ 1:13 PM
NCT ID:
NCT06272695
Eligibility Criteria:
Inclusion Criteria:
* Receiving insulin for the treatment of documented diagnosis of T1DM for at least 2 years
* Body Mass Index (BMI) of 18.5 kg/m2 to 35.0 kg/m2
* On treatment with a stable insulin regimen for at least 8 weeks
* Currently using a continuous glucose monitoring (CGM) system
* HbA1c less than or equal to 10.0%
* Females of non-childbearing potential must be ≥1 year post-menopausal or documented as being surgically sterile. Females of childbearing potential must agree to use two methods of contraception during the entire study and for an additional 3 months after the end of dosing with the investigational product
* Male subjects must be willing to use clinically acceptable method of contraception during the entire study and for an additional 3 months after the end of the treatment period
* Other inclusion criteria may apply.
Exclusion Criteria:
* History of type 2 diabetes, maturity onset diabetes of the young (MODY), pancreatic surgery or chronic pancreatitis
* Pancreas, pancreatic islet cells, or renal transplant recipient
* T1DM treatment with any other antihyperglycemic drug (e.g., metformin, alpha- glucosidase inhibitors, SGLT-2 inhibitors, pramlintide, inhaled insulin, pre-mixed insulins, etc.) within 30 days of Day 1
* Occurrence of severe hypoglycemia involving coma and/or seizure that required hospitalization or hypoglycemia-related treatment by an emergency physician or paramedic within 3 months prior to Day 1
* Myocardial infarction, unstable angina, revascularization procedure, or cerebrovascular accident ≤12 weeks
* Indication of liver disease
* Current signs and symptoms of anemia
* Untreated eating disorders such as bulimia or anorexia nervosa
* History of pancreatitis, pancreatic neuroendocrine tumors or multiple endocrine neoplasia (MEN) or family history of MEN.
* Treatment with systemic corticosteroids within 30 days of Day 1, or planned initiation of such therapy during the study.
* Medical history of cancer or treatment for cancer in the last five years
* Women who are pregnant, nursing, or who plan to become pregnant while in the trial
* Other exclusion criteria may apply
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
72 Years
Study:
NCT06272695
Study Brief:
Protocol Section:
NCT06272695