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A Research Study to See How a Weekly Insulin, Insulin Icodec, Helps in Reducing the Blood Sugar Compared to Daily Insulin Glargine, Both in Combination With Insulin Aspart, in Adults With Type 1 Diabetes
NCT07076199 · View on ClinicalTrials.gov ↗
Study Summary
This study compares insulin icodec, an insulin taken once a week to insulin glargine, an insulin taken once a day. The study medicine will be investigated in participants with type 1 diabetes. The study will look at how well insulin icodec taken weekly controls blood sugar compared to insulin glargine taken daily. The study will last for about 8.5 months.
Conditions Studied
Interventions
- DRUG Insulin aspart
- DRUG Insulin icodec
- DRUG Insulin glargine
Study Locations (20)
California
- John Muir Health — Concord
- Headlands Research California, LLC — Escondido
- Clinical Res of Central Ca — Fresno
- Providence Medical Foundation — Fullerton
- Scripps Whittier Diabetes Inst — La Jolla
- Loma Linda University Faculty Medical Clinics — Loma Linda
- Loma Linda University Faculty Medical Clinics — Loma Linda
- Pacific Clinical Studies — Los Alamitos
- Pasadena Clinical Trials — Pasadena
- WestenU Health — Pomona
- WestenU Health — Pomona
- Alliance Clinical Network — San Diego
- Mills Health Center — San Mateo
- Center for Endocrine DM and Metabolic Disorders — Santa Clarita
- University Clin Investigators — Tustin
- Diablo Clinical Research, Inc. — Walnut Creek
Colorado
- Denver Endocrinology Diabetes and Thyroid Center — Englewood
- Optumcare Clinical Trials,LLC-Golden — Golden
Alabama
- Cullman Clinical Trials — Cullman
Florida
- Northeast Research Institute — Fleming Island
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 877 participants |
| Start Date | 2025-08-11 |
| Est. Completion | 2026-12-28 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07076199
The ClinicalTrials.gov registry entry for NCT07076199 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 877 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novo Nordisk A/S, which has 189 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Diabetes Mellitus, Type 1 appearing as the primary indexed condition, and to 3 interventions — of which Insulin aspart is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07076199 reports 20 study locations spanning 4 distinct geographic areas — top geographies include California, Colorado, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07076199 about?
NCT07076199 is a clinical study titled "A Research Study to See How a Weekly Insulin, Insulin Icodec, Helps in Reducing the Blood Sugar Compared to Daily Insulin Glargine, Both in Combination With Insulin Aspart, in Adults With Type 1 Diabetes". This study compares insulin icodec, an insulin taken once a week to insulin glargine, an insulin taken once a day. The study medicine will be investigated in participants with type 1 diabetes. The study will look at how well insulin icodec taken weekly controls blood sugar compared to insulin glargi...
What is the current status of trial NCT07076199?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 877 participants. The study started on 2025-08-11. Estimated completion is 2026-12-28.
What conditions does trial NCT07076199 study?
This clinical trial studies the following conditions: Diabetes Mellitus, Type 1. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07076199?
The interventions under investigation include: Insulin aspart (DRUG), Insulin icodec (DRUG), Insulin glargine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07076199?
This trial is sponsored by Novo Nordisk A/S, which has 189 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07076199 being conducted?
This trial has 20 study locations across Alabama, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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