Tirabrutinib is developed from Japan. It’s a second generation Bruton’s tyrosine kinase inhibitor. We conducted a Phase II study of tirabrutinib monotherapy for symptomatic Waldenstrom’s patients. 27 patients enrolled on the study and with a median follow-up duration of two years the major response rate was 93% and two-year progression-free survival was 92% and overall survival is 100%...
Tirabrutinib is developed from Japan. It’s a second generation Bruton’s tyrosine kinase inhibitor. We conducted a Phase II study of tirabrutinib monotherapy for symptomatic Waldenstrom’s patients. 27 patients enrolled on the study and with a median follow-up duration of two years the major response rate was 93% and two-year progression-free survival was 92% and overall survival is 100%. So regarding toxicity, it’s very safe and as for hypertension, bleeding tendency, and arrythmia, it’s very limited. On the other hand very mild skin-related adverse event is recognized in about half but we can easily manage them. And as for the tirabrutinib for Bing-Neel syndrome it’s a very interesting topic for now and we have many case reports treated by tirabrutinib for Bing-Neel syndrome and the penetration rate of the tirabrutinib into the blood-brain barrier is very high, 13 to 18 percent according to the report from the tirabrutinib for primary CNS lymphoma relapsed refractory cases.