Celerion, Phoenix
Tempe, Arizona, 85283, United States
NCT Number: NCT07605052
The purpose of this clinical study is to compare 2 different versions cagrilintide and see how these work in people living with excess body weight. Participant will get either cagrilintide B or cagrilintide D injections. Which treatment participant will get is decided by chance. Participant will be in this clinical study for about 14 weeks.
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Notify Me18 year–64 year
All sexes
Interventional
Phase 1
Tempe, Arizona, 85283, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Cagrilintide B will be administered subcutaneously.
Cagrilintide D will be administered subcutaneously.
Time frame: From Pre-dose at Day 29 to Day 36
Measured as hour*nanomole per liter (h*nmol/L).
Time frame: From Pre-dose at Day 29 to Day 36
Measured as nanomole per liter (nmol/L).
Time frame: From Pre-dose at Day 22 to Day 29
Measured as h*nmol/L.
Time frame: From Pre-dose at Day 22 to Day 29
Measured as nmol/L.
Time frame: From Pre-dose at Day 1 to Day 8
Measured as h*nmol/L.
Time frame: From Pre-dose at Day 1 to Day 8
Measured as nmol/L.
Novo Nordisk A/S
Industry
Investigation of Pharmacokinetics of Two Different Presentations of Cagrilintide in Participants With Overweight and Obesity
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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