LivingGLP1
Study S002236

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

Registration

Registration
NCT07430059
Acronym
SLIM-1
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
NOT_YET_RECRUITING
Enrollment
20
Start
2026-07
Primary completion
2026-12
Lead sponsor
Vivani Medical, Inc
Conditions
Obesity & Overweight
Interventions
COMBINATION_PRODUCT:Semaglutide Implant (NPM-139); DRUG:Semaglutide (Wegovy) weekly injection
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Area under the plasma concentration-time curve (AUC) [4 weeks]
  • Maximum plasma concentration (Cmax) [4 weeks]
  • Time to maximum semaglutide concentration (Tmax) [4 weeks]
  • Adverse Events [4 weeks]

Linked records (0)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.

No records link to this registration yet.