Rare blood cancer approval for Imbruvica in Rituxan combo
Imbruvica (ibrutinib) has received US approval in combination with rituximab as the first chemotherapy-free combination in adults with Waldenström's macroglobulinemia.
As a monotherapy, Imbruvica was approved by the US Food and Drug Administration (FDA) in this rare blood cancer, an incurable type of non-Hodgkin’s lymphoma (NHL), in January 2015.
Imbruvica is a Bruton's tyrosine kinase (BTK) inhibitor jointly developed and commercialized by Pharmacyclics, an AbbVie (NYSE: ABBV) company, and Janssen Biotech, part of US healthcare giant Johnson & Johnson (NYSE: JNJ).
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