Overview

Bioequivalence Study of Sorafenib Tablet and Nexavar

Status:
Completed
Trial end date:
2015-10-01
Target enrollment:
Participant gender:
Summary
Randomized, open-label, 3-way reference replicated crossover bioequivalence study of sorafenib 200 mg tablet and nexavar (reference) following a 200 mg dose in healthy subjects under fasting conditions.
Phase:
Phase 1
Details
Lead Sponsor:
Yabao Pharmaceutical Group
Treatments:
Niacinamide
Sorafenib