DOSING &
ADMINISTRATION
Grace
Person with PH1*

*Alnylam is proud to feature real patients in our advertising. Patients may or may not be on an Alnylam therapy.

OXLUMO® (lumasiran) is a subcutaneous injection dosed by weight1

Administered via subcutaneous injection by a healthcare professional1

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3 monthly starting doses aim to reduce oxalate levels1

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Ongoing dosing beginning one month after the last
starting dose aims to sustain the reduction1

Recommend dosing regimen base on actual body weight1

OXLUMO is administered via subcutaneous injections. The first 4 doses of OXLUMO are composed of 3 monthly starting doses followed by the first ongoing dose beginning 1 month after the last starting dose.

3 starting doses: 3 mg/kg administered monthly

3mg/kg dose

Start

3mg/kg dose

Month 1

3mg/kg dose

Month 2

Ongoing dosing: 3 mg/kg administered quarterly beginning one month after the last starting dose

3mg/kg dose

Month 3

No dose

Month 4

No dose

Month 5

3mg/kg dose

Month 6

Ongoing quarterly dosing continues past month 6

Download the Dosing Guide

3 starting doses: 6 mg/kg administered monthly

6mg/kg dose

Start

6mg/kg dose

Month 1

6mg/kg dose

Month 2

Ongoing dosing: 6 mg/kg administered quarterly beginning one month after the last starting dose

6mg/kg dose

Month 3

No dose

Month 4

No dose

Month 5

6mg/kg dose

Month 6

Ongoing quarterly dosing continues past month 6

Download the Dosing Guide

3 starting doses: 6 mg/kg administered monthly

6mg/kg dose

Start

6mg/kg dose

Month 1

6mg/kg dose

Month 2

Ongoing dosing: 3 mg/kg administered monthly beginning one month after the last starting dose

3mg/kg dose

Month 3

3mg/kg dose

Month 4

3mg/kg dose

Month 5

3mg/kg dose

Month 6

Ongoing monthly dosing continues past month 6

Download the Dosing Guide

If your patient misses a dose
If a dose is delayed or missed, administer OXLUMO as soon as possible and resume prescribed regimen from the most recently administered dose.1

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OXLUMO Administration

  • Doses are typically administered in office
  • Some patients may qualify to receive the injection at home from a healthcare professional, depending on their insurance coverage
  • No dose adjustment is necessary in patients with renal impairment, including kidney failure, or those on hemodialysis

For patients on hemodialysis, administer OXLUMO following hemodialysis if administered on dialysis days.

See full Prescribing Information for detailed steps on how to prepare and administer OXLUMO.

Show Me the Prescribing Information

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WANT TO SPEAK WITH AN OXLUMO REPRESENTATIVE?

Our representatives are available to provide detailed information about OXLUMO and how it may help your patients with PH1.

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Alnylam Assist™ Logo

Alnylam Assist™ provides support services for your patients throughout their treatment with OXLUMO.

Alnylam Assist™ includes patient services in key areas, including understanding insurance benefits and financial assistance options, helping ensure access to therapy, and providing PH1 disease education.

Take Me to the Start Form

Reference: 1. OXLUMO [Package Insert]. Cambridge, MA. Alnylam Pharmaceuticals, Inc.

IMPORTANT SAFETY INFORMATION

Adverse Reactions
The most common (≥20%) adverse reaction reported in patients treated with OXLUMO was injection site reaction. Injection site reactions included erythema, swelling, pain, hematoma, pruritus, and discoloration.

Pregnancy and Lactation
No data are available on the use of OXLUMO in pregnant women. No data are available on the presence of OXLUMO in human milk or its effects on breastfed infants or milk production. Consider the developmental and health benefits of breastfeeding along with the mother’s clinical need for OXLUMO and any potential adverse effects on the breastfed child from OXLUMO or the underlying maternal condition.

INDICATION

OXLUMO is indicated for the treatment of primary hyperoxaluria type 1 (PH1) to lower urinary and plasma oxalate levels in children and adults.

For additional information about OXLUMO, please see the full Prescribing Information.