The purpose of this study is to assess the relative bioavailability of branebrutinib tablet
formulation relative to the capsule formulation in order to identify doses that would provide
exposures similar to the capsule formulation over the dose range that may be used in future
clinical studies, evaluate the effect of food on the bioavailabi...Read More
lity of branebrutinib from a
tablet formulation at a dose projected to provide similar pharmacokinetics (PK) as the 9 mg
capsule formulation, and evaluate the safety and the PK of multiple oral dose of tablet
formulation of branebrutinib in healthy participants.Read Less
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