Coherus Hoping For Expedited FDA Review Of Pegfilgrastim On-Body

Biosimilar Humira Sales Won’t Accelerate Until 2025; Pleased With Ranibizumab Execution

Coherus BioSciences offered clarity and insight into its three marketed biosimilar products, as the firm continues to await USFDA approval for its pegfilgrastim biosimilar using an on-body injector device.

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“Given there is not any new information to review,” Coherus BioSciences continues to anticipate approval from the “resource-constrained” US Food and Drug Administration for the company’s version of Amgen’s Neulasta (pegfilgrastim) Onpro on-body injector device using Coherus’ Udenyca (pegfilgrastim-cbqv) biosimilar “this year or in the early part of 2024.”

While pivoting towards a more novel biologics strategy, Coherus’ plotted return to growth for Udenyca is important in the next couple of years given that the firm concedes it will not see significant growth for its adalimumab biosimilar,

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