French biotech Nicox (Euronext Paris: COX) is confident that – together with its partners – it can overcome the concerns of the US Food and Drug Administration (FDA) in relation to its key products, latanoprostene bunod and AC-170.
The ophthalmic research and development company has updated investors on the progress of the two eye care treatments, the prompt approval of which are key to Nicox’s development plans for other candidates.
Bausch + Lomb, a wholly-owned subsidiary of Canadian drugmaker Valeant Pharmaceuticals International (TSX: VRX) and Nicox’ licensee for latanoprostene bunod, expects the launch of latanoprostene bunod to take place in mid-2017.
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