A Study Comparing the Injection Site Pain Experience After the Injection of Semaglutide B and Semaglutide D With 2 Different Injection Pens, a Compound for the Treatment of Type 2 Diabetes and Obesity
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT04143945
- Phase
- PHASE2
- Status
- Completed
Conditions
- Healthy Volunteers Diabetes Mellitus, Type 2
- Healthy Volunteers Obesity
- Healthy Volunteers Overweight
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Accepted
Interventions
- Semaglutide (administered by DV3396 pen) — DRUGSubjects will receive 1 single dose of semaglutide 0.25 mg on 1 day
- Semaglutide (administered by PDS290 pen) — DRUGSubjects will receive 1 single dose of semaglutide 0.25 mg on 1 day
Study Details
This study in healthy men and women looks at the injection site experience of the DV3396 pen to that of the PDS290 pens when both pens are used to deliver 0.25 mg semaglutide subcutaneously (s.c., under the skin). Participants will receive 2 single doses of semaglutide 0.25 mg on 1 day. The 2 injections will be given at least 30 minutes apart, one in each side of the stomach. Participants will be in the clinic research center for 1 day. A follow-up phone call will take place between 4 and 5 weeks after the injections were given.
Key Dates
- Start date
- Oct 28, 2019
- Status verified
- Dec 2020
- Primary completion
- Jan 4, 2020
- Completion
- Jan 4, 2020
Study Design
- Enrollment
- 104 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- TREATMENT
Arms
- Experimental: DV3396 followed by PDS290The 2 treatments will be administered at least 30 minutes apart, one in each side of the stomach
- Experimental: PDS290 followed by DV3396The 2 treatments will be administered at least 30 minutes apart, one in each side of the stomach
Primary Outcome Measure
Intensity of Injection Site Pain [ Time Frame: After 1 minute of each injection (Day 1) ]