drugset / Trial / NCT00714584
Pharmacokinetics of Naltrexone Following Intravenous and Oral Routes of Administration in Healthy Volunteers
RandomizedCrossoverOpen-labelTreatment
Summary
The purpose of the study is to compare the pharmacokinetics of naltrexone following i.v. and oral administration in healthy volunteers, and to assess the bioavailability of naltrexone following oral administration. Moreover, safety is assessed.
Timeline
- Start
- 2003-05
- Primary completion
- —
- Completion
- 2003-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Naltrexone | Small molecule | 1 mg | Intravenous |
| Subject | Naltrexone | Small molecule | 50 mg | Intravenous |
Indications
No indication recorded.