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Not Yet RecruitingNCT07415954

A Research Study Comparing How Well Different Doses of the Medicine NNC0662-0419 Lower Blood Sugar in People With Type 2 Diabetes

Efficacy and Safety of Once-weekly Subcutaneous NNC0662-0419 in Participants With Type 2 Diabetes - a Dose-finding Study

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
270 (estimated)
Sponsor
Novo Nordisk A/S · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is being done to look at the effect and safety of different doses of NNC0662-0419 in people living with type 2 diabetes when compared to placebo or semaglutide. The purpose of this clinical study is to find out if NNC0662-0419 is effective and safe for treating people living with type 2 diabetes. Participants will get either NNC0662-0419, semaglutide or placebo. Which treatment participants get is decided by chance. NNC0662-0419 is a new medicine which cannot be prescribed by doctors but has previously been tested in humans. Semaglutide is an approved medication to treat type 2 diabetes.

Conditions

Interventions

TypeNameDescription
DRUGNNC0662-0419NNC0662-0419 will be administered subcutaneously.
DRUGSemaglutideSemaglutide will be administered subcutaneously.
DRUGPlaceboPlacebo will be administered subcutaneously.

Timeline

Start date
2026-04-17
Primary completion
2027-09-03
Completion
2027-09-03
First posted
2026-02-17
Last updated
2026-03-11

Locations

63 sites across 10 countries: United States, Croatia, Hungary, Japan, Poland, Portugal, Slovakia, South Korea, Spain, Thailand

Regulatory

Source: ClinicalTrials.gov record NCT07415954. Inclusion in this directory is not an endorsement.