Biosimilar company Sandoz has announced the launch of a new global initiative to take on worldwide health inequities.
Act4Biosimilars aims to increase patient access to advanced medicines by leveraging the ‘4 As’ of biosimilars – approvability, accessibility, acceptability and affordability. The initiative is supported by a multidisciplinary steering committee of patient advocacy leaders, healthcare professionals, biosimilar experts and industry leaders from across the world.
Other notable targets of the project include ensuring equitable pricing, involving patients in treatment decisions and streamlining biosimilar development. The ultimate goal is to increase global adoption of biosimilar medicines by at least 30% throughout 30 countries by 2030.
“As a result of their affordability, biosimilars have opened up a new realm of possibility for patients by enabling biological medicines to become more widely available to those in need of these advanced, life-changing treatments,” explained Zorana Maravic, CEO at Digestive Cancers Europe. “However, until we address existing biosimilar access inequities, far too many patients will continue to miss out on treatment with the best possible medicines.”
“Healthcare systems are facing more pressure than ever before, which can be attributed to the costs associated with a growing, ageing population, more people being diagnosed with chronic diseases,” added Richard Saynor, chief executive officer at Sandoz. “Biosimilars are part of the solution to support a more sustainable healthcare system for all and we are proud to be the founding sponsor of Act4Biosimilars, which will drive action to bring these more affordable treatment options to patients who need them.”
The Steering Committee is currently developing an action plan to provide the strategies, tools and activities required to realise the global ambitions. This will be supported by country indicator maps to measure the change that is being driven by groups, associations and organisations worldwide.
A biosimilar is a biological medicine which is produced after the original therapy’s patent has expired. Biosimilars also match all the required treatment references in terms of quality, safety and efficacy.
Sandoz developed and brought the first biosimilar medicine to patients 16 years ago.
by John Pinching
Source: pharmatimes.com
CordenPharma announced its largest strategic investment to date, committing to spend ~€900m over the next three years to enhance its peptide technology platform. The planned investment consists of two major expansion initiatives occurring in parallel in the US and Europe, including both existing facilities and new constructions.
DSM-Firmenich has announced the sale of its MEG-3 fish oil business to KD Pharma Group, a contract development and manufacturing organisation that is active in pharmaceutical and nutritional lipids. As part of the transaction, DSM-Firmenich will obtain a minority stake of 29% in KD Pharma’s parent company O³ Holding GmbH.
Veranova, a development and manufacturing of specialist and complex APIs for the pharmaceutica l and biotech sectors, recently announced the appointment of Cécile Maupas as Senior Vice President, Chief Commercial Officer. Cécile will join the executive team and assume responsibility for business development, marketing, project management, commercial operations, and product management.
