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Nick Sireau
@Nick_Sireau
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I'm the father of two children with Alkaptonuria (AKU), a rare genetic disease; the CEO&Chairman of @AKUSociety; and Chairman of @findacure_fdn. My views.
Cambridge
Joined November 2012
Motivations for joining a trial: results of a cystic fibrosis patient study. Oli Rayner @cftrust #trialsconf
http://t.co/IdxfoJRoZM
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Pharmacomedics' Kamlesh Sheth says patient groups should seek out champions for their cause in industry #trialsconf
http://t.co/GF7AbFwb7i
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@AKUSociety's Hana Ayoob explains to @findacure_fdn workshop how to make patients central to clinical trials http://t.co/BmA59yHwQn
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Bruce Bloom @CuresWReach says socialfinancing can help drug repurposing at Boston drug repositioning conference
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#BlackBoneDisease: the world's 1st #genetic disease, discovered more than 110 years ago. It's time to cure it. http://t.co/nGpLZ0KMQx
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Making good progress with #aku team at #hopitalnecker discussing #clinicaltrial protocol for #developakure.
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Our recruitment drive for AKU patients for our clinical trials is accelerating: http://t.co/wJ152k4QzE
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Mutual trust crucial for high quality research says Myrovlytis Trust CEO John Solly at #orphanconf
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Myrovlytis Trust's CEO John Solly looks at challenges involved in setting up medical foundation @ #orphanconf
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AFM's CSO announces upcoming launch of French venture philanthropy fund for rare diseases at #orphanconf
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Great presentation by AFM's CSO on how AFM patient group has funded new drug discovery models #orphanconf
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Sobi CEO Geoffrey McDonough made excellent presentation on AKU programme on ntbc at #orphanconf today.
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