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NOT YET RECRUITING
NCT07430059
PHASE1

Safety, Tolerability and Pharmacokinetics of a Subcutaneous Semaglutide Implant

Sponsor: Vivani Medical, Inc

View on ClinicalTrials.gov

Summary

The study will evaluate the safety, tolerability and drug levels of a semaglutide implant placed just under the skin for a period of 4 weeks compared to 4 weekly injections of semaglutide (Wegovy) in overweight/obese participants who are otherwise healthy..

Official title: A Randomized, Parallel-Group Study to Assess the Safety, Tolerability, and Pharmacokinetics of Semaglutide Implant

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2026-04

Completion Date

2026-09

Last Updated

2026-02-24

Healthy Volunteers

No

Interventions

COMBINATION_PRODUCT

Semaglutide Implant (NPM-139)

Semaglutide Implant (NPM-139) is a drug/device combination product consisting of a subdermal titanium implant \~23 mm long and 2 mm in diameter, containing a sterile liquid formulation of semaglutide that is released from the implant at a substantially constant rate over at least 15 weeks.

DRUG

Semaglutide (Wegovy) weekly injection

Semaglutide (Wegovy) is a clear, colorless solution provided as Wegovy FlexTouch four-dose pens: 0.25 mg/0.5 mL. It is injected SC in the abdomen, thigh or upper arm once/week.