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Development of orphan medical products | 18131
Journal of Genetic Syndromes & Gene Therapy

Journal of Genetic Syndromes & Gene Therapy
Open Access

ISSN: ISSN: 2157-7412

+44 1223 790975

Development of orphan medical products


2nd World Congress on Rare Diseases and Orphan Drugs

June 29-30, 2017 London, UK

Martine Zimmermann

Alexion Pharmaceuticals, Inc., Switzerland

Scientific Tracks Abstracts: J Genet Syndr Gene Ther

Abstract :

Overview: This track will discuss opportunities and challenges associated with developing drugs for rare and ultra-rare diseases, and the use of novel approaches to bridge these challenges and successfully bring important lifesaving therapies to patients in need. Context/Details: Between 5,000 and 8,000 districts, rare diseases exist affecting around 27 million to 36 million people in the European Union. Collectively, these diseases represent a significant proportion of the population, and a growing healthcare concern since many of these rare disorders are serious conditions with no approved treatments. Since roughly 80% of these diseases have identified genetic origin, our scientific understanding of and ability to target these diseases is growing. Technological advances and our increased understanding of underlying disease biology has aided in the development of several groundbreaking therapies over the past ten years. In addition, heightened public policy support and push to find treatments for patients with rare and devastating diseases has helped in the adoption of legislative vehicles and regulatory programs that compliment scientific discovery and provide important development and financial incentives to companies to bring new targets from bench to bedside. Among them include expedited development and approval programs that offer enhanced regulatory dialogue and support for developers from early stages of clinical development through to approval. More and more we see appreciable regulatory support for innovative program design and increased regulator openness in applying regulatory flexibilities. All these factors have aided in the approval of important medicines for ultra-rare and devastating diseases. Yet challenges do persist in the development process; chief among them is the absence of knowledge about the disease itself, which is needed to inform important aspects of clinical development. Natural history for rare diseases is often poorly described or missing altogether given the small affected populations who themselves have variable phenotypes and clinical courses. For developers, it is important, early in the development process, to assess the depth and quality of this information so that a parallel study might better inform the development process. In this track, we will discuss the pathway to the development of rare diseases, starting with this most critical first step of assessing and acquiring knowledge of the disease itself through natural history studies. We will discuss endpoint selection, innovative design and leveraging expedited programs to help with small data sets. We will discuss ways in which frequent and early communication is essential. Finally, we will bring all these points together by using a real life example/case study.

Biography :

Martine Zimmermann is a Vice President of Global Regulatory Affairs at Alexion. She is based in Zurich. She has over 20 years of combined R&D and global regulatory strategy experience. She joined Alexion in 2009 and since then has been dedicated to the registration of orphan medical products as well as shaping a favorable regulatory environment for orphans Throughout her career, she has been directly involved in multiple regulatory approvals across the globe and most recently Strensiq approval in 2015 in Japan, Europe and US. She received her PharmD from University Louis Pasteur in Strasbourg (France).

Email: martine.zimmermann@alexion.com

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