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BioPharmaceutical

Genentech’s Lucentis BLA Will Not Include Data Supporting Dosing Advantage

This article was originally published in Pharmaceutical Approvals Monthly

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  • Pharmaceutical Approvals Monthly

Executive Summary

FDA's decision to deny Genentech fast-track status for Lucentis (ranibizumab) means that the initial submission for the wet age-related macular degeneration therapy, slated for December, will not include data supporting a dosing advantage

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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