drugset / Trial / NCT00447187

Study to Assess the Efficacy and Safety of LX201 for Prevention of Corneal Allograft Rejection Episodes and Graft Failure in Subjects at Increased Immunological Risk

NCT00447187 ↗

Phase 3 Terminated 368 enrolled Lux Biosciences, Inc.
RandomizedParallel-groupSingle-blindPrevention

Summary

This was a pivotal trial to determine whether LX201 reduces the likelihood of a graft rejection episode following corneal transplantation in patients at high immunological risk for rejection.

Timeline

Start
2007-04
Primary completion
2009-03
Completion
2010-11

Outcome

Outcome not reported

Stopped: “The primary efficacy endpoint was not met”

Drugs

EvaluationDrugModalityDoseRoute
Subject LX201 Unknown 30 % Other

Indications