A 36 month observational study to describe the long-term efficacy and safety of ranibizumab 0.5 mg treatment in patients with visual impairment due to choroidalneovascularization (CNV) secondary to pathologic myopia (PM)

10/03/2015
02/07/2024
EU PAS number:
EUPAS8816
Study
Finalised
Documents
Study protocol
Initial protocol
English (2.13 MB - PDF) View document
Study results
Study results
English (494.72 KB - PDF) View document
Study report
Other information