Trials / Completed
CompletedNCT03512821
A Single-dose, Comparative Bioavailability Study of Two Formulations of Ursodiol 500mg Tablets Under Fed Conditions
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 77 (actual)
- Sponsor
- Daewoong Pharmaceutical Co. LTD. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
single-dose, comparative bioavailability study of two formulations of ursodiol 500mg tablets under fed conditions
Detailed description
A single-dose, comparative bioavailability study of two formulations of ursodiol 500mg tablets under fed conditions: open label, single-dose, randomized, two-period, two-treatment, two-sequence, crossover, comparative bioavailability study
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ursodiol 500 MG | Ursodiol 500mg tablets followed by Urso Forte 500mg tablets |
| DRUG | Urso Forte 500Mg Tablet | Urso forte 500mg tablets followed by Ursodiol 500mg tablets |
Timeline
- Start date
- 2017-10-01
- Primary completion
- 2017-11-30
- Completion
- 2017-11-30
- First posted
- 2018-05-01
- Last updated
- 2018-05-07
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT03512821. Inclusion in this directory is not an endorsement.