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Study identifier: NCT06062069 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: Completed

A Study of CT-868 in Type 1 Diabetes Mellitus

Condition: Overweight · Obese · Type 1 Diabetes Mellitus  ·  Sponsor: Carmot Therapeutics, Inc.

PhasePhase 2
Planned participants111
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where22 locations
For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.Open the site landscape →

About this study

This study will evaluate the changes in glycemic control in overweight and obese adults with Type 1 Diabetes Mellitus after receiving CT-868 for 16 weeks. The effectiveness and safety of CT-868 will be compared to placebo. All participants will continue with their standard diabetes care using either an insulin pump (CSII) or multiple daily injections (MDI). Alongside their designated treatment, participants will receive guidance on managing their diabetes, including monitoring blood glucose levels and diet and exercise recommendations. Treatment assignments, either CT-868 plus insulin or placebo plus insulin will be randomly determined.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Male or female, 18 years of age or older at the time of signing informed consent * Have a documented clinical diagnosis of T1DM greater than or equal to 1 year before the Screening Visit * Body mass index greater than or equal to27.0 kg/m2 * Hemoglobin A1c (HbA1c) level between 7.0% and 10.0%, inclusive, at the Screening Visit Exclusion Criteria: * Diagnosis of Type 2 diabetes mellitus (T2DM) or any other types of diabetes, except T1DM * Experienced diabetic ketoacidosis (DKA) within 3 months prior to the Screening Visit * Experienced severe hypoglycemia (Level 3 as defined in the ADA Standards of Medical Care in Diabetes (ADA 2022) within 3 months prior to the Screening Visit

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (22)

John Muir Physician Network Clinical Research CenterConcord, California, United States
Headlands Research- AMCREscondido, California, United States
University of Colorado - Barbara Davis Center for DiabetesAurora, Colorado, United States
Denver Endocrinology Diabetes and Thyroid CenterEnglewood, Colorado, United States
Advent HealthOrlando, Florida, United States
Orlando Health Science Clinic, LLCOrlando, Florida, United States
Innovative Research InstitutePort Charlotte, Florida, United States
Atlanta Diabetes AssociatesAtlanta, Georgia, United States
Rocky Mountain Clinical Research, LLC- Idaho Falls, IdahoIdaho Falls, Idaho, United States
Iowa Diabetes and Endocrinology Research CenterWest Des Moines, Iowa, United States
MedStar Health Research Institute - Washington Hospital CenterHyattsville, Maryland, United States
University of North Carolina Health Sciences at MAHECAsheville, North Carolina, United States

+ 10 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

ConcordEscondidoAuroraEnglewood

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