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Remibrutinib

RHAPSIDO

Remibrutinib ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Remibrutinib ballicule

What it isAn oral covalent BTK inhibitor for chronic spontaneous urticaria not controlled by antihistamines.

Why this oneIt is an oral alternative to injectable biologics and requires no routine laboratory monitoring.

What limits itBleeding changes prescribing; interrupt around surgery and weigh antithrombotics. Avoid strong or moderate CYP3A4 inhibitors or inducers.

Remibrutinib molecular structure (skeletal formula)
Molecular structure: Remibrutinib

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Chronic spontaneous urticaria (symptomatic despite H1 antihistamine treatment)Adults25 mg BID25 mg BID25 mg BID

Renal Undefined

Hepatic Avoid use in mild, moderate, or severe hepatic impairment (Child-Pugh A, B, and C) — exposure increased

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy Insufficient human data; rabbit external malformations at exposures 141x MRHD; pregnancy exposure registry available (Novartis 1-888-669-6682)

Lactation No data in human or animal milk; weigh benefits of breastfeeding against maternal need and potential infant risk

Cost

Remibrutinib (RHAPSIDO)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/mobrand $/moCostPlus
25 mgtab60 BID—$4,347.73not offered

NO BOXED WARNINGS

Principal riskBleeding

Classes and tags

Clinical profile

Therapeutic safety burden2 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk2 / 4

Legacy pregnancy categoryN/A (post-2015 labeling)

Defining liabilityBleeding and perioperative interruption

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