eBook: The Future of Monoclonal Antibody Manufacturing — Incremental Improvement or Industrial Revolution?

Dan Stanton, Managing editor

May 24, 2018

2 Min Read

16-5-MAbs-eBook-229x300.jpgMonoclonal antibody manufacturing is at a crossroads. Biomanufacturers could continue exploring new technologies and fine-tuning proven systems such as mammalian cell expression systems in stirred-tank bioreactor fed-batch
cultures. But some experts say an opportunity is arising to turn the industry on its head by taking lessons from other branches of bioprocessing, such as the industrial enzyme sector.

Drug makers are criticized often these days for the high prices of their products. The lay media, governments, payers, and patients themselves all have voiced their share of grievances against “Big Biopharma’s” pricing strategies. For example, Alexion’s monoclonal antibody (MAb) eculizumab (Soliris) was questioned in a 2014 guidance from the UK National Institute for Health and Care Excellence (NICE), the independent drug assessment body for the National Health Service (NHS) in England and Wales. The agency demanded to know why, from a manufacturing viewpoint, the atypical hemolytic-uremic syndrome (aHUS) treatment was priced at £3,150 (US$4,280) per 30-mL vial. That equates to £340,200 ($460,000) to treat one patient over 12 months, which is over 30× price of other antibodies on the market. This is an extreme example, but other MAbs are far from inexpensive.

“The annual acquisition cost of adalimumab (Humira) to the NHS is £9,295 per patient (based on 26 injections per year),” NICE wrote in a 2010 guidance document recommending AbbVie’s bestselling MAb (1). The agency eventually recommended that the NHS in England and Wales fund Soliris, recognizing its value to patients despite not being presented “with a justification of why the overall cost of eculizumab was materially higher than the overall cost of other highly specialized

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