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FDA approves Lucentis (ranibizumab injection) for myopic choroidal neovascularisation
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This approval is based on the results of the Phase III RADIANCE study, which demonstrated that treatment with Lucentis provided superior visual acuity gains in people with mCNV compared to verteporfin photodynamic therapy (vPDT). At three months, average visual acuity gains for patients treated with Lucentis were more than 12 letters, compared to 1.4 letters for those treated with vPDT.
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Related Keywords Ranibizumab Injection, Lucentis, Myopic Choroidal Neovascularisation