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The Social Security Financing Bill (PLFSS) for 2021, which is due back for a new reading in the National Assembly on Monday, is the concrete expression of an ambitious reform of early access to innovative drugs that AGIPHARM has long been calling for.
The implementation of this reform will be crucial if the new system is to deliver on its promises for the benefit of patients.
In the wake of the Economic Recovery Plan, the government and the President of the Republic have called for a reform of the ATU system. Pierre-Claude Fumoleau, President of AbbVie France and of Agipharm, the association of innovative American pharmaceutical companies in France, welcomes this step forward for patients suffering from serious diseases and for innovation in France.
“The response to the Covid-19 crisis cannot be reduced to a proliferation of health nationalisms. On the contrary, it must be based on the pooling of intelligence and skills ”
In the context of the Covid-19 crisis, more and more voices are being raised to restore health independence in France and Europe, highlighting the need to prevent drug shortages and to revive the national territory's attractiveness.
However, positions on this subject often limit the concept of "health independence" to the relocation of production alone, while it involves many other concepts, both crucial and strategic. Moreover, this vision exposes France to a number of risks such as retaliatory measures that could encourage the emergence of drug shortages.
Therefore, AGIPHARM defines health independence more as the ability of a state to guarantee patients effective and secure access to health products and presents its proposals to achieve this goal.
Pierre-claude Fumoleau, president of the French subsidiary of AbbVie, has been elected president of AGIPHARM. He succeeds Michel Joly, President of Gilead France. Under the aegis of its new president, AGIPHARM will continue its work in close association with Leem, of which it is a member, but also with all decision-makers and actors in the health system to advance three major priorities: '' patient access to drugs, in particular by reviewing the conditions for early access to therapeutic innovation, modernizing the drug evaluation system to adapt it to the new challenges of therapeutic innovation, and finally recreating the conditions for growth for companies in the sector, in order to support investment in tomorrow's treatments, on French territory, and for the provision of new therapeutic solutions to patients.
Cancers, hepatitis, autoimmune or rare diseases… Why do French patients later have access to therapeutic innovations? In this forum, the "ACCèS +" collective, made up of health professionals, patient associations and players in the health industries, calls out to the public authorities and proposes solutions.
Seagen, formerly Seattle Genetics, is a Seattle-based biotechnology company founded in 1998 by scientist Clay Siegall, who continues to lead the company today.
Seagen is dedicated to the field of oncology and our mission is to discover, develop and commercialise high-potential targeted therapies that can change the prognosis and management of cancer patients.
Our focus and strategy has always been to use the most innovative scientific technologies to develop next-generation biotherapies for advanced, difficult-to-treat cancers. To make the fruits of our R&D investments available to professionals and patients even more quickly, we have until now favoured a cooperative model with a strong spirit of partnership.
For the first time, in 2020, Seagen decided to market one of its products under its own name in metastatic breast cancer and has therefore very recently established itself in various European countries with the opening of different subsidiaries, including France where the status of Pharmaceutical Laboratory Operator was obtained in February 2021.
Vertex is an international biotechnology company investing in scientific research to create innovative medicines for patients with serious diseases. In Europe, four Vertex drugs are approved for the treatment of the underlying cause of cystic fibrosis, a rare, multi-systemic, life-threatening disease. The company is also conducting several clinical trials in cystic fibrosis. Vertex's deep understanding of human biology also provides a portfolio of drugs under investigation for other serious diseases such as sickle cell disease, beta thalassaemia, pain, alpha-1 antitrypsin deficiency, Duchenne muscular dystrophy and APOL1-mediated kidney disease.
Founded in 1989 in Cambridge, Massachusetts, Vertex Pharmaceuticals' global headquarters are now based in Boston's Innovation District, with international headquarters in London. The company now has research and development centres and operating subsidiaries in the United States, Europe, Canada, Australia and Latin America. Vertex Pharmaceuticals is recognised among the best companies in the industry for its quality of work life. Vertex opened its subsidiary in France in 2012.