DRUG
CT-868
CT-868
Status
Completed
Phase
Phase 1
Enrollment
32
Locations
1
Results
Not posted
Publications
0
Study summary
This study will be conducted primarily to evaluate the effects of CT-868 on glucose homeostasis in participants with Type 1 Diabetes Mellitus.
Interventions
DRUG
CT-868
DRUG
Placebo as SC Injection
DRUG
Victoza as active comparator as SC Injection
Timeline
First posted
Apr 3, 2023
Study start
Mar 21, 2023
Primary completion
Mar 6, 2024
Study completion
Apr 6, 2024
Results posted
Not reported
Registry updated
Dec 27, 2024
Outcomes
To assess area under the curve (AUC) in glucose metabolism during MMTT
Time frame · Baseline up to 4 days
To assess changes in continuous glucose monitoring (CGM) measures
Time frame · Baseline up to 4 days
Area under the acetaminophen concentration-time (AUC)
Time frame · 0 - 300 minutes
Eligibility
Inclusion Criteria: * Female or male adults with Type 1 diabetes * Ages 18-65 years * Type 1 DM for at least 3 years * Using an insulin pump or multiple daily injections (MDI) for at least 3 months * BMI 25.0 - 35.0 Exclusion Criteria: * Significant medical history * Uncontrolled diabetes * History of surgical treatment for weight loss * History of malignancy
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Carmot Clinical Research Unit 101
Chula Vista, California, United States
Publications
No PMID-linked publications were present in this registry snapshot.
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