drugset / Trial / NCT06132867

A Study to Compare the Relative Bioavailability of Brigatinib When Swallowed as a Solution Versus When Swallowed as a Tablet in Healthy Adults

NCT06132867

Phase 1 Completed 12 enrolled Takeda
RandomizedCrossoverOpen-labelBasic science

Summary

The main aim of this study is to compare the amount of brigatinib in the blood of healthy adults after they have swallowed one dose either as a solution or as a tablet.

Timeline

Start
2023-12-20
Primary completion
2024-02-17
Completion
2024-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Brigatinib Small molecule 90 mg Oral

Indications

No indication recorded.