Status:
COMPLETED
Research Study to Investigate How a Study Medicine (NNC9204- 1177) Affects Blood Levels of Other Medicines in Healthy People
Lead Sponsor:
Novo Nordisk A/S
Conditions:
Healthy Volunteers
Overweight
Eligibility:
All Genders
18-60 years
Phase:
PHASE1
Brief Summary
The study looks at how the study medicine (NNC9204-1177) affects other medicines in the body. Participants will get the study medicine and 5 other medicines which have all been approved by the authori...
Eligibility Criteria
Inclusion
- Male or female, aged 18-60 years (both inclusive) at the time of signing informed consent.
- Body mass index (BMI) between 23.0 and 29.9 kg/m\^2 (both inclusive) at screening.
- Considered to be generally healthy based on the medical history, physical examination, and the results of vital signs, electrocardiogram (ECG) and clinical laboratory tests performed during the screening visit, as judged by the investigator.
Exclusion
- Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using a highly effective contraceptive method (intra-uterine device (IUD), vasectomised partner or sexual abstinence)
- Any disorder, which in the investigator's opinion might jeopardise subject's safety or compliance with the protocol.
- Use of prescription medicinal products or non-prescription drugs, except for IUDs, within 14 days prior to the day of screening.
- Use of any herbal medicine known to interfere with the metabolic CYP pathways, such as Hypericum (St. John's Wort), ginseng, garlic, milk thistle, and echinaceae, within 14 days prior to the day of screening.
Key Trial Info
Start Date :
August 15 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 2 2020
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT04059367
Start Date
August 15 2019
End Date
January 2 2020
Last Update
January 22 2020
Active Locations (1)
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1
Novo Nordisk Investigational Site
San Antonio, Texas, United States, 78209