Genmab — November 2013
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http://www.news-medical.net/news/20130829/FDA-approves-NDA-filing-for-ibrutinib-inhibitor-in-two-B-cell-malignancies.aspx 2,5 måned efter FDAs acceptance kom approval
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J&J får hurtig FDA-godkendelse
FDA har godkendt et lægemiddel fra Johnson & Johnson til behandling af lymfekræft efter en ualmindelig kort evalueringsperiode på blot fire måneder. Det er blot anden gang, at et lægemiddel bliver godkendt under FDAs specielle Breakthrough-program.
(medwatch.dk)
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Ibrutinib sælges for 20$ pr. pille
det svarer til 130.000$ om året pr. patient i Mantle cell så vidt jeg kan se !!! 
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the agency's accelerated approval program, which allows the FDA to approve a drug to treat a serious disease based on clinical data showing that the drug has an effect on a surrogate endpoint that is reasonably likely to predict a clinical benefit to patients
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Among the 19 patients evaluable for response, overall response rate was 94%, with CR in 17 patients, partial remission in one patient and progressive disease after the second cycle in one patient; 15 out of 15 patients evaluable for minimal residual disease in the BM showed molecular remission.
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