drugset / Trial / NCT02017730

To Evaluate The Relationship Between Plasma Drug Levels And Receptor Binding in Lung Using PET (Positron Emission Tomography) In Healthy Volunteers

NCT02017730

Phase 1 Completed 20 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to assess the safety and tolerability of a novel positron emission tomography (PET) tracer \[11C\]BMT-136088 in healthy adult subjects for measurement of availability of Lysophosphatidic Acid (LPA1) receptors in the human lung and to use this tracer to assess LPA1 receptor occupancy using \[11C\]BMT-136088 in the human lung following oral administration of Bristol Myers Squibb (BMS)-986020.

Timeline

Start
2014-01
Primary completion
2015-01
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986020 Small molecule 50 mg Oral
Subject BMS-986020 Small molecule 150 mg Oral
Subject BMS-986020 Small molecule 300 mg Oral
Subject BMS-986020 Small molecule 600 mg Oral
Subject BMS-986020 Small molecule 1200 mg Oral
Subject BMS-986020 Small molecule 1500 mg Oral
Subject [11C]BMT-136088 Diagnostic / imaging agent Intravenous

Indications

No indication recorded.