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Professor Valérie Cormier-Daire, recipient of the 2024 Pasteur-Weizmann/Servier Prize for her work on the treatment for rare bone anomalies in children

It is estimated that between 150-225 million children live with a rare disease worldwide1. Some of the most well-known include osteogenesis imperfecta or “brittle bone disease,” cystic fibrosis, Duchenne muscular dystrophy, and Sanfilippo syndrome. 

The innovative work of Professor Valérie Cormier-Daire and her teams has been highly praised, along with her major advancements in understanding and treating rare childhood diseases. Her research has opened up new and promising perspectives for improving the care of young patients suffering from these complex and often debilitating conditions.

In his closing speech, Olivier Laureau paid tribute to researchers and clinicians. He emphasized the crucial role of scientific research in transforming the lives of children with rare diseases: “Medical research is about giving the best of oneself to improve and save lives, and that is the most beautiful thing.”

About the Pasteur-Weizmann/Servier Prize:

Since 2003 L’Institut Servier has partnered with the Institut Pasteur/Weizmann Institute of Sciences Council to award the Pasteur-Weizmann/Servier International Prize (250,000 euros) to a researcher, a medical doctor or a scientist for major contribution to a biomedical discovery determining a major therapeutic application.

The objective of the prize is to promote and encourage fundamental research, in particular the transition from laboratory research to medical therapy. Founded in 1999, L’Institut Servier is a non-profit association under French law.


[1] Source: Nguengang Wakap, S., Lambert, D.M., Olry, A. et al. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database.