Glenmark Pharma reports Phase 1 results supporting biosimilarity criteria for GBR 310

26 Jul 2018 Evaluate

Glenmark Pharmaceuticals has reported results from a Phase 1 study that suggest similarity in pharmacokinetic, pharmacodynamic, safety and immunogenicity profiles between Glenmark’s GBR 310 proposed biosimilar and reference product omalizumab, marketed in the US under the brand name Xolair.

GBR 310 is a recombinant DNA-derived humanized immunoglobulin G1 kappa monoclonal antibody. The proposed indications for GBR 310 are for the treatment of allergic asthma and chronic idiopathic urticaria (CIU).

According to IQVIA sales data for the 12-month period ending May 2018, annual sales of Xolair were approximately $2 billion in the US.

Glenmark Pharmaceuticals is a global pharmaceutical company. The company is engaged in the development of new chemical entities (NCEs) and new biological entities (NBEs). Its segments are India, United States, Latin America, Europe and Rest of the World (ROW).

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