NN9388-7700: Efficacy and safety of co-administered cagrilintide s.c. 2.4 mg in combination with semaglutide s.c. 2.4 mg (cagrisema s.c. 2.4 mg/2.4 mg) once-weekly compared to semaglutide, cagrilinitide and placebo in people with chronic kidney disease and type 2 diabetes.
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Enrollment
This study is currently enrolling. -
Research Area
Translational Research -
Location
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Principal Investigator
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Sponsor
Novo Nordisk
Study Purpose: The purpose of this study is to see whether CagriSema can lower kidney damage. This will be compared to the effects of semaglutide, cagrilintide and placebo.
Study Duration: Approximately 35 weeks
Study Commitment: 10 outpatient visits
3 phone calls
Age: 18+ years old
Sex: Male & Female
Conditions/Eligibility: You have chronic kidney disease.
You have type 2 diabetes.
Your Body Mass Index is at least 27 kg/m2.
Study Procedures: Informed consent
Medical history and medication review
Questionnaires and medication diary
Electrocardiogram (ECG)
Eye exams
Urine and blood collections
Compensation: Up to $1,300.00
Enrollment Form
This study is currently enrolling.