drugset / Trial / NCT01072214

A Safety Study to Evaluate Pazopanib Eye Drops in Healthy Volunteers

NCT01072214

Phase 1 Completed 37 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindTreatment

Summary

A study to determine the safety and tolerability of pazopanib eye drops. The study will also determine how the drug is absorbed and metabolized over time. Repeat doses of eye drops will be administered to healthy adult volunteers over a 14-day period with one additional dose given on the 15th day of the session. Three groups of subjects may receive either active drug or placebo (drops without drug). The first group of subjects will receive a maximum of 1.6mg of pazopanib or placebo. The dose of drug to be given to the next two groups will be determined based on the results of the first group of subjects. The last group of subjects will be of Japanese descent.

Timeline

Start
2010-03-09
Primary completion
2010-06-28
Completion
2010-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Pazopanib Small molecule 1.6 mg Other

Indications