For US Healthcare Professionals Only

These resources are available for your patients with indolent systemic mastocytosis (ISM) to learn more about AYVAKIT

Patient Brochure for ISM

A guide to AYVAKIT for ISM, including clinical trial data, safety and dosing information, and patient access.

Download Patient Brochure

Patient Education Events

Your patients can hear directly from doctors and patients about AYVAKIT as a treatment option for ISM.

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Patient Events
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AYVAKIT Mentor Program

Patients can speak directly to another patient about their experience with AYVAKIT and ISM

Learn MoreDownload Link

Doctor Discussion Guide

An interactive tool to help prepare your patients for conversations with their HCPs to discuss treatment goals.

See Doctor Discussion GuideDownload Link

AYVAKIT ISM Welcome Kit

The Welcome Kit contains resources and materials that can help your patients with ISM make the most of their experience with AYVAKIT. Patients can request a Welcome Kit once prescribed AYVAKIT.

AYVAKIT® (avapritinib) Welcome Kit for patients
Have questions about managing ISM or prescribing AYVAKIT?
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INDICATION

AYVAKIT® (avapritinib) is indicated for the treatment of adult patients with indolent systemic mastocytosis (ISM).

Limitations of Use: AYVAKIT is not recommended for the treatment of patients with ISM with platelet counts of <50 x 109/L.

IMPORTANT SAFETY INFORMATION
INDICATION & IMPORTANT SAFETY INFORMATION

Cognitive Effects—Cognitive adverse reactions can occur in patients receiving AYVAKIT and occurred in 7.8% of patients with ISM who received AYVAKIT + best supportive care (BSC) versus 7.0% of patients who received placebo + BSC; <1% were Grade 3. Depending on the severity, withhold AYVAKIT and then resume at the same dose, or permanently discontinue AYVAKIT.

Photosensitivity—AYVAKIT may cause photosensitivity reactions. In all patients treated with AYVAKIT in clinical trials (n=1049), photosensitivity reactions occurred in 2.5% of patients. Advise patients to limit direct ultraviolet exposure during treatment with AYVAKIT and for one week after discontinuation of treatment.

Embryo-Fetal Toxicity—AYVAKIT can cause fetal harm when administered to a pregnant woman. Advise pregnant women of the potential risk to a fetus. Advise females and males of reproductive potential to use an effective contraception during treatment with AYVAKIT and for 6 weeks after the final dose. Advise women not to breastfeed during treatment with AYVAKIT and for 2 weeks following the final dose.

Adverse Reactions—The most common adverse reactions (10%) in patients with ISM were eye edema, dizziness, peripheral edema, and flushing.

Drug Interactions—Avoid coadministration of AYVAKIT with strong or moderate CYP3A inhibitors or inducers. If contraception requires estrogen, limit ethinyl estradiol to 20 mcg unless a higher dose is necessary.

To report suspected adverse reactions, contact Blueprint Medicines Corporation at 1-888-258-7768 or the FDA at 1-800-FDA-1088 or visit www.fda.gov/medwatch.

Please click here to see the full Prescribing Information for AYVAKIT.

References:

  1. AYVAKIT [prescribing information]. Cambridge, MA: Blueprint Medicines Corporation; November 2024.
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  6. Data on file. Blueprint Medicines Corporation, Cambridge, MA. 2023.
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  18. Akin C, ed. Mastocytosis: A Comprehensive Guide. Springer; 2020.