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Sarclisa

Sarclisa

Manufacturer:

Sanofi-Aventis Deutschland
Information is sourced from publicly available references. The information is for educational purpose of healthcare professionals and we are not liable for any loss or damage.
Core Prescribing Info
Contents
Isatuximab
Indications/Uses
In combination w/ pomalidomide & dexamethasone for adult patients w/ relapsed & refractory multiple myeloma who have received at least 2 prior therapies including lenalidomide & a proteasome inhibitor & have demonstrated disease progression on the last therapy; w/ carfilzomib & dexamethasone for adult patients w/ relapsed or refractory multiple myeloma who have received 1-3 prior therapies.
Dosage/Direction for Use
Premed Administer 15-60 min prior to starting Sarclisa infusion. Dexamethasone 40 mg PO or IV (or 20 mg PO or IV for patients ≥75 yr) when administered in combination w/ isatuximab & pomalidomide. Dexamethasone 20 mg (IV on the days of isatuximab &/or carfilzomib infusions, & PO on the other days) when administered in combination w/ isatuximab & carfilzomib. Acetaminophen 650-1,000 mg PO (or equiv). Diphenhydramine 25-50 mg IV or PO [or equiv (eg, cetirizine, promethazine, dexchlorpheniramine)]. IV Adult Recommended dose: 10 mg/kg wkly for cycle 1 (days 1, 8, 15, 22) then every 2 wk for cycle 2 (days 1, 15) & beyond; repeat until disease progression or unacceptable toxicity.
Contraindications
Hypersensitivity.
MIMS Class
Targeted Cancer Therapy
ATC Classification
L01FC02 - isatuximab ; Belongs to the class of CD38 (Clusters of Differentiation 38) inhibitors. Used in the treatment of cancer.
Presentation/Packing
Form
Sarclisa conc for soln for infusion 20 mg/mL
Packing/Price
1's
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