Dr Reddy’s gets US FDA approval for rituximab biosimilar
Dr Reddy’s Laboratories received US FDA approval for its rituximab biosimilar for the US market. The monoclonal antibody biosimilar of Rituxan targets CD20 on B lymphocytes and was developed, manufactured and submitted by Dr Reddy’s. Under a commercialisation agreement, Fresenius Kabi has exclusive rights to commercialise in the US.