Oxlumo

— THERAPEUTIC CATEGORIES —
  • Inborn errors of metabolism

Oxlumo Generic Name & Formulations

General Description

Lumasiran 94.5mg/0.5mL; per vial; soln for SC inj; preservative-free.

Pharmacological Class

HAO1-directed small interfering ribonucleic acid.

How Supplied

Single-dose vial—1

Generic Availability

NO

Oxlumo Indications

Indications

Treatment of primary hyperoxaluria type 1 (PH1) to lower urinary and plasma oxalate levels.

Oxlumo Dosage and Administration

Adults and Children

Give by SC inj into abdomen, thigh, or upper arms; rotate inj sites. <10kg: loading dose: 6mg/kg once monthly for 3 doses; maintenance (begin 1 month after the last loading dose): 3mg/kg once monthly. 10–<20kg: loading dose: 6mg/kg once monthly for 3 doses; maintenance (begin 1 month after the last loading dose): 6mg/kg once every 3 months. ≥20kg: loading dose: 3mg/kg once monthly for 3 doses; maintenance (begin 1 month after the last loading dose): 3mg/kg once every 3 months. Hemodialysis patients: administer dose after session if given on dialysis days.

 

Oxlumo Contraindications

Not Applicable

Oxlumo Boxed Warnings

Not Applicable

Oxlumo Warnings/Precautions

Warnings/Precautions

Severe hepatic impairment (total bilirubin >3×ULN with any AST) or peritoneal dialysis patients: not studied. Pregnancy. Nursing mothers.

Oxlumo Pharmacokinetics

See Literature

Oxlumo Interactions

Not Applicable

Oxlumo Adverse Reactions

Adverse Reactions

Inj site reactions, abdominal pain.

Oxlumo Clinical Trials

See Literature

Oxlumo Note

Not Applicable

Oxlumo Patient Counseling

See Literature

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