Biocon has received marketing authorization from the Drugs Controller General (India) (DCGI) for its biosimilar Trastuzumab being developed jointly with Mylan, for the treatment of Her 2+ metastatic breast cancer. The regulatory approval for biosimilar Trastuzumab in India is an important milestone for Biocon as it is the world’s first biosimilar version of Herceptin to be brought to the market. The biosimilar Trastuzumab will be marketed in India under the brand name of CANMAb by Biocon and is expected to be available to Indian patients in Q4 FY14.
Kiran Mazumdar Shaw, Chairperson and Managing Director, Biocon, said, “This is a major milestone for both partners as it is the world’s first biosimilar Trastuzumab to be accorded regulatory approval. We plan to make CANMAb available to Indian patients in Q4 FY14. The meticulous development of this important cancer drug has involved extensive product characterisation and clinical trials to demonstrate comparability and similarity in PK (pharmacokinetic), safety, efficacy and immunogenicity against the innovator product. We are committed to affordable cancer care and believe that biosimilar Trastuzumab will expand patient access to this life saving drug. The Indian approval is an encouraging milepost as we plan to leverage this data to support regulatory filings in several countries across the globe.” The global sales for Trastuzumab stood at ~$6.4 billion in 2012, while in India it recorded sales of ~$21 million.
Since 2009, Biocon and Mylan have been co-developing a high value portfolio of Biosimilar monoclonal antibodies and complex biologics, comprising Trastuzumab, Pegfilgrastim, Bevacizumab, Adalimumab and Etanercept. The innovator product sales of these products in 2012 were pegged at ~ $34 billion. The patent expiry of these products in regulated markets is expected from 2015 onwards. In 2013, this partnership was extended to co-development of Biosimilar insulin analogs for the global markets.
EP News Bureau – Mumbai
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