WHO Project To Prequalify Biosimilar Cancer Medicines Aims At Increased Affordability04/05/2017 by Intellectual Property Watch 1 CommentShare this Story:Click to share on Twitter (Opens in new window)Click to share on LinkedIn (Opens in new window)Click to share on Google+ (Opens in new window)Click to share on Facebook (Opens in new window)Click to email this to a friend (Opens in new window)Click to print (Opens in new window)IP-Watch and its Global Health Policy News are non-profit independent news services and depend on subscriptions. To access all of our content, please subscribe now. You may also offer additional support with your subscription, or donate.The World Health Organization announced today that it will launch a pilot project in 2017 for prequalifying cancer biosimilar medicines, with the intent of lowering prices on some of the most expensive cancer treatments. Biosimilars are medicines very similar to the original biotherapeutics, which are pharmaceutical products derived from biological and living sources. They are often “speciality drugs,” highly effective in treating medical conditions for which no other treatments are available, in particular cancer, and chronic diseases such as diabetes. However those medicines are also highly priced, according to the WHO.The WHO press release states that the pilot project will be a “step towards making some of the most expensive treatments for cancer more widely available in low-and middle-income countries.”According to the release, the WHO will invite manufacturers to submit applications for prequalification of biosimilar versions of two products in the WHO Essential Medicines List: rituximab (used principally to treat non-Hodgkin’s lymphoma and chronic lymphocytic leukemia), and trastuzumab (used to treat breast cancer).Biotherapeutics cannot be copied in the same way traditional medicines can, and no generic version of a biotherapeutic can be produced. Biosimilar products have to be comparable to the originator products in terms of quality, safety and efficacy, according to the WHO. If biosimilars submitted for prequalification meet those requirements, the medicines will be listed by WHO and become eligible for procurement by United Nations agencies, the release said.As generic versions of branded medicines, biosimilars are expected to be cheaper than the original biotherapeutic. WHO “will advocate for fairer prices for all biotherapeutics to ensure that these treatments can truly benefit public health,” according to the release.The decision comes after a two-day meeting in Geneva between WHO, national regulators, pharmaceutical industry groups, patient and civil society groups, payers and policymakers to discuss ways to increase access to biotherapeutic medicines, says the release. Share this Story:Click to share on Twitter (Opens in new window)Click to share on LinkedIn (Opens in new window)Click to share on Google+ (Opens in new window)Click to share on Facebook (Opens in new window)Click to email this to a friend (Opens in new window)Click to print (Opens in new window)Related"WHO Project To Prequalify Biosimilar Cancer Medicines Aims At Increased Affordability" by Intellectual Property Watch is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.