drugset / Trial / NCT02231671

A Phase 1, Open-Label Study of the Absorption, Metabolism, Excretion and Absolute Bioavailability of ALS-008176

NCT02231671

Phase 1 Completed 12 enrolled Alios Biopharma Inc.
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to see how ALS-008176 is taken up, broken down, and removed from the body.

Timeline

Start
2014-08-31
Primary completion
2014-09-30
Completion
2014-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ALS-008112 Unknown 100 ug Intravenous
Subject Lumicitabine Small molecule 375 mg Oral