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Investigating How CagriSema, Semaglutide and Cagrilintide Regulate Insulin Effects in the Body of People With Type 2 Diabetes - Trial NCT06403761

Access comprehensive clinical trial information for NCT06403761 through Pure Global AI's free database. This Phase 1 trial is sponsored by Novo Nordisk A/S and is currently Not yet recruiting. The study focuses on Diabetes Mellitus, Type 2. Target enrollment is 150 participants.

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NCT06403761
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06403761
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Investigating How CagriSema, Semaglutide and Cagrilintide Regulate Insulin Effects in the Body of People With Type 2 Diabetes
Effect of CagriSema, Semaglutide and Cagrilintide on Insulin Sensitivity and Pancreatic Endocrine Function in Adults With Type 2 Diabetes

Study Focus

Diabetes Mellitus, Type 2

Semaglutide

Interventional

drug

Sponsor & Location

Novo Nordisk A/S

Neuss, Germany

Timeline & Enrollment

Phase 1

May 06, 2024

Dec 18, 2025

150 participants

Primary Outcome

To compare the effect of CagriSema versus placebo: Change in M-value in hyperinsulinaemic euglycaemic clamp (HEC)

Summary

This study will look at how CagriSema, semaglutide and cagrilintide regulate insulin effects
 in the body of people with type 2 diabetes (T2D). CagriSema is a new investigational medicine
 that combines two medicines called cagrilintide and semaglutide. Doctors may not yet
 prescribe CagriSema. Participants will either get CagriSema, semaglutide, cagrilintide, or a
 ''dummy'' medicine. Which treatment the participants will get is decided by chance.
 Participants will get the study medicine together with the current daily diabetes medicine
 metformin. Participants should not take other medicines for diabetes during the study. The
 study will last for about 42 weeks.

ICD-10 Classifications

Type 2 diabetes mellitus
Type 2 diabetes mellitus with unspecified complications
Type 2 diabetes mellitus with other specified complications
Type 2 diabetes mellitus without complications
Type 2 diabetes mellitus with multiple complications

Data Source

ClinicalTrials.gov

NCT06403761

Non-Device Trial