drugset / Trial / NCT02252354

TAK-385 Phase I Absorption, Distribution, Metabolism, Excretion and Absolute Bioavailability Study

NCT02252354

Phase 1 Completed 12 enrolled Takeda
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this 2 part study is to look at how TAK-385 is taken up, broken down and removed from the body when given as a radiolabelled oral solution (by mouth) or as an oral tablet (by mouth) followed by a radiolabelled intravenous (IV) infusion (into the arm vein).

Timeline

Start
2014-09
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Relugolix Small molecule 80 ug Oral
Subject Relugolix Small molecule 80 mg Oral

Indications

No indication recorded.