Repeat-dose toxicity (26-week rat, 39-week dog) exposure multiples 15- to 146-fold human steady-state AUC
“No remibrutinib-related adverse effects were observed in the 39-week dog toxicity study (doses up to 300 mg/kg/day), and adverse effects on the endocrine pancreas observed at all tested dose levels in the 26-week rat toxicity study (doses up to 1,000 mg/kg/day) were considered unlikely to translate to human. Exposure multiples ranged from 15- to 146-fold in terms of steady-state AUC0-24h.”
“Target organs of toxicity were identified as the lymph nodes (underdeveloped germinal centers, sinusoidal red blood cells), thyroid gland (follicular hypertrophy), liver (hepatocellular hypertrophy, multinucleated hepatocytes, pigment), pancreas (islet fibrosis, pigment), and blood (prolongation of bleeding, inhibition of platelet aggregation).”