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Clinical Trial Summary

This study is designed as an exploratory study to assess safety and efficacy of two different doses of the anti-VEGF agent ranibizumab (0.12 mg vs. 0.20 mg) in the treatment of infants with retinopathy of prematurity. Furthermore it shall help to improve safety in the treatment of ROP and provide explorative data on long-term effects of ranibizumab after intravitreal injection in neonates.

The primary objective is to assess clinical efficacy of ranibizumab in children with ROP


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02134457
Study type Interventional
Source University Hospital Freiburg
Contact
Status Completed
Phase Phase 2
Start date August 2014
Completion date January 2017

See also
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