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...






