A Research Study to Compare Two Different Versions of Injectable CagriSema in People With Type 2 Diabetes
Part of paid clinical trials in Little Rock, Arkansas.
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT07357740
- Phase
- PHASE2
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 64 Years
- Healthy Volunteers
- Not accepted
Interventions
- CagriSema — DRUGCagrilintide and Semaglutide will be administered subcutaneously using device 1 or device 2.
- Placebo CagriSema — DRUGPlacebo matched to Cagrilintide and Placebo matched to Semaglutide will be administered subcutaneously using device 1 or device 2.
Study Details
This study is being done to look at how well a study medicine called CagriSema helps people with diabetes lower their blood sugar. In this study the sponsor will compare two version of CagriSema injected by two different types of injection devices. Which treatment participants get is decided by chance. CagriSema is still being tested in studies and is not yet available for doctors to prescribe. The study will last for about 38 weeks.
Key Dates
- Start date
- Aug 27, 2026
- Status verified
- Mar 2026
- Primary completion
- Aug 25, 2027
- Completion
- Oct 13, 2027
Study Design
- Enrollment
- 400 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: CagriSema in device 1 + Placebo CagriSema B in device 2Participants will receive CagriSema in device 1 followed by placebo matched to CagriSema B in device 2 subcutaneously once weekly in a dose escalation manner.
- Experimental: CagriSema B in device 2 + Placebo CagriSema in device 1Participants will receive CagriSema B in device 2 followed by placebo matched to CagriSema in device 1 subcutaneously once weekly in a dose escalation manner.
Primary Outcome Measure
Change in glycated haemoglobin (HbA1c) [ Time Frame: Baseline to week 28 ]
Central Contacts
- Novo Nordisk(+1) 866-867-7178
Locations (21)
Find similar trials in Little Rock, AR
Related Studies
- Pre-diabetes in Subject With Impaired Fasting Glucose (IFG) and Impaired Glucose Tolerance (IGT)Recruiting · The University of Texas Health Science Center at San Antonio · San Antonio, Texas
- Use of CGM in Kidney Transplant RecipientsRecruiting · University of California, Davis · Sacramento, California
- Promoting Preconception Care and Diabetes Self-Management Among Reproductive-Aged Women With DiabetesRecruiting · Northwestern University · Chicago, Illinois
- Food as Medicine for HIV and DiabetesRecruiting · University of North Carolina, Chapel Hill · Chapel Hill, North Carolina