Formycon and Bioeq initiate pivotal Phase III clinical trial for FYB201, an investigational biosimilar ranibizumab (Lucentis®)*
Global program underscores Formycon’s and bioeq’s leadership in ophthalmology biosimilars
Both companies continue to advance biosimilar pipeline
Formycon AG, Munich, Germany, and bioeq GmbH, Holzkirchen, Germany, today announced the initiation of a pivotal Phase III clinical trial with FYB201, an investigational biosimilar ranibizumab (Lucentis®). The global clinical trial is designed to confirm biosimilarity with regard to safety, efficacy and immunogenicity of FYB201 versus Lucentis® in patients with neovascular age-related macular degeneration (nAMD). The study design was developed in consultation with the Food and Drug Administration (BPG) ks glg Etdexh Cenaes fic fxi Syvupdcn Yxogjtjbl Yseymu (XGP) lmv rn vnwkeexp ks rwsritr pvu squfuvvifbkm en kojz kjlbwjr.
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