drugset / Trial / NCT03143712

Study to Assess Bioavailability of GLPG1690 Given as Oral Capsule or Tablet

NCT03143712

Phase 1 Completed 12 enrolled Lakefront Biotherapeutics NV
RandomizedCrossoverOpen-labelTreatment

Summary

This study is a Phase I, randomized, open-label, cross-over study with three single-dose treatments to compare the bioavailability of an oral tablet relative to an oral capsule of GLPG1690 after single dose intake in healthy male subjects and to evaluate the effect of food on the bioavailability of the oral tablet.

Timeline

Start
2017-04-18
Primary completion
2017-06-14
Completion
2017-06-14

Drugs

EvaluationDrugModalityDoseRoute
Subject ZIRITAXESTAT Small molecule 600 mg Oral

Indications

No indication recorded.