RecruitingPhase 3NCT07076199
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
Studying Disorder of carbohydrate metabolism
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Novo Nordisk A/S
- Principal Investigator
- Clinical Transparency (dept. 2834)Novo Nordisk A/S
- Intervention
- Insulin icodec(drug)
- Enrollment
- 877 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2027
Study locations (30)
- Cullman Clinical Trials, Cullman, Alabama, United States
- John Muir Health, Concord, California, United States
- Headlands Research California, LLC, Escondido, California, United States
- Clinical Res of Central Ca, Fresno, California, United States
- Providence Medical Foundation, Fullerton, California, United States
- Scripps Whittier Diabetes Inst, La Jolla, California, United States
- Loma Linda University Faculty Medical Clinics, Loma Linda, California, United States
- Pacific Clinical Studies, Los Alamitos, California, United States
- Los Angeles Institute for Metabolic Research, Los Angeles, California, United States
- Pasadena Clinical Trials, Pasadena, California, United States
- WestenU Health, Pomona, California, United States
- Alliance Clinical Network, San Diego, California, United States
- Mills Health Center, San Mateo, California, United States
- Center for Endocrine DM and Metabolic Disorders, Santa Clarita, California, United States
- University Clin Investigators, Tustin, California, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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