drugset / Trial / NCT04991571

Study to Collect Samples for MIST Analysis of Zibotentan and Bioavailability of Zibotentan and Dapagliflozin in Heatlhy Participants

NCT04991571

Phase 1 Completed 27 enrolled AstraZeneca
RandomizedCrossoverOpen-labelTreatment

Summary

The study will have 2 independent parts: Part 1 of the study is intended to collect samples for Metabolites in Safety Testing (MIST) analysis after administration of multiple doses of zibotentan. Part 2 of the study is designed to evaluate the relative bioavailability of zibotentan and dapagliflozin after dosing with two different fixed-dose combination (FDC) formulations and dosing with separate formulations of zibotentan and dapagliflozin.

Timeline

Start
2021-07-29
Primary completion
2021-10-22
Completion
2021-10-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Dapagliflozin Small molecule Oral
Subject Zibotentan Small molecule Oral