LivingGLP1
Study S000701

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

Registration

Registration
NCT05670379
Acronym
LIBERATE-1
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
24
Start
2024-12-20
Primary completion
2025-08-21
Lead sponsor
Vivani Medical, Inc
Conditions
Overweight and Obesity; Type2diabetes
Interventions
COMBINATION_PRODUCT:Exenatide Implant; DRUG:Bydureon BCise (exenatide extended release); DRUG:Semaglutide, 1.0 mg/mL
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Area under the plasma concentration-time curve (AUC) [9 weeks]
  • Maximum plasma concentration observed (Cmax) [9 weeks]
  • Time to maximum plasma concentration observed (Tmax) [9 weeks]
  • Adverse events [9 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.