Sweden’s Xbrane Biopharma says it is “on track” to obtain an EU marketing authorization for the firm’s Xlucane (ranibizumab) proposed biosimilar to Lucentis before the expiry of patents shielding the blockbuster eye-disease treatment in July 2022, despite challenges posed by the accelerating COVID-19 crisis.
In the firm’s annual report published on 16 April, the biosimilars and long-acting injectables specialist outlines several key goals in...






