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FDA grants Breakthrough designation to ibrutinib in cGVHD

The US Food and Drug Administration (FDA) has granted a fourth Breakthrough Therapy Designation for ibrutinib (Imbruvica) as monotherapy for the treatment of patients with chronic graft-versus-host-disease (cGVHD) after failure of one or more lines of systemic therapy.


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source: http://www.europeanpharmaceuticalreview.com/42180/news/industry-news/fda-ibrutinib-cgvhd/

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