Pfizer has been backed to receive a European Union- (EU-) wide marketing authorization approval for the firm’s Avastin (bevacizumab) biosimilar but has also shelved one of its two Humira (adalimumab) biosimilar applications, a 'limited label' filing with indications carved out, for strategic reasons.
During the December meeting of the European Medicines Agency's (EMA’s) Committee for Medicinal Products for Human Use (CHMP), the committee adopted a positive opinion recommending the granting
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