drugset / Trial / NCT01423149

Safety and Efficacy Study of Combretastatin A4 Phosphate to Treat Patients With Choroidal Neovascularization Secondary to Pathologic Myopia

NCT01423149

Phase 2 Completed 23 enrolled Mateon Therapeutics
Non-randomizedParallel-groupDouble-blindTreatment

Summary

The objectives of this study are to evaluate the safety and efficacy of 3 dose groups (27, 36 and 45 mg/m2) of Combretastatin A-4 Phosphate for the treatment of subfoveal choroidal neovascularization in subjects with pathologic myopia.

Timeline

Start
2005-03
Primary completion
2007-01
Completion
2007-01

Drugs

EvaluationDrugModalityDoseRoute
Subject fosbretabulin Small molecule 27 mg/m2
Subject fosbretabulin Small molecule 36 mg/m2
Subject fosbretabulin Small molecule 45 mg/m2