drugset / Trial / NCT04716881

Pharmacokinetic Study of Vivitrol in Healthy Participants

NCT04716881

NaSingle-groupOpen-labelBasic science

Summary

This is a Phase I, single-center, single arm, open-label study, to establish the pharmacokinetic (PK) parameters of Vivitrol 380 mg IM injection (IP), a US Food and Drug Administration (FDA) approved medication.

Timeline

Start
2021-01-25
Primary completion
2022-04-04
Completion
2022-04-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Naltrexone Small molecule 380 mg Intramuscular

Indications