The US Food and Drug Administration has set a goal date under the Biosimilar User Fee Act of 27 November 2021 for Bio-Thera Solutions’ BAT1706 biosimilar bevacizumab candidate, having accepted for filing the Chinese firm’s biologics license application referencing Roche’s Avastin oncology blockbuster.
Bio-Thera is seeking approval for its biosimilar from the FDA for all US-licensed Avastin indications, including metastatic colorectal cancer and non-squamous non-small cell lung cancer
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