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Collaborating to Treat Rare Diseases

Posted on November 16th, 2016 by in Pharma R&D

DDD magazine

There are about 7,000 diseases out there that are considered “rare,” but they actually affect hundreds of millions of people worldwide – nearly half of whom are children. The vast majority of them have no approved drug treatment. The reason is because developing new drugs is so terribly costly for pharmaceutical companies that it is seldom economically feasible to focus on treatments that only help a small number of people.

It’s precisely because R&D is so expensive that drug re-purposing is becoming a common way for companies to bring “new” drugs to market. And, thanks to a combination of increasingly sophisticated data, analytical tools and growing interest in precision medicine, drug re-purposing is opening up new avenues for developing rare disease treatments. However, to find success in targeting rare diseases, pharma companies must welcome collaborative efforts – with bioinformatics companies, academic institutions and beyond.

To find out more about how innovative partnerships can tackle rare disease, read Tim Hoctor’s article Repurposing Drugs for Rare Diseases: Collaboration is Key.


All opinions shared in this post are the author’s own.

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