Clinical trial
A 2-Part, Phase I, Single Dose, Crossover Relative Bioavailability Study of Both TIVICAY 10 mg Conventional Tablets and 5 mg Dispersible Tablets Compared to Conventional TIVICAY Tablets in Fasted Healthy Adult Subjects
NCT03095638 is registered in ClinicalTrials.gov with ViiV Healthcare as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A 2-Part, Phase I, Single Dose, Crossover Relative Bioavailability Study of Both TIVICAY 10 mg Conventional Tablets and 5 mg Dispersible Tablets Compared to Conventional TIVICAY Tablets in Fasted Healthy Adult Subjects
- Lead sponsor
- ViiV Healthcare
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- May 3, 2017
- Completion date
- June 23, 2017
- Enrollment
- 38 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.