For adults and children 1 year and older with AML with an NPM1 mutation whose disease has come back or has not improved after previous treatment(s) and who have no other satisfactory treatment options

NEW APPROVAL

Revuforj® (revumenib) Logo Read the MED GUIDE/IFU

Introducing Revuforj for NPM1m AML

Finally, there’s an FDA-approved targeted treatment specifically for patients 1 year and older who have acute myeloid leukemia (AML) with a nucleophosmin 1 (NPM1) mutation, whose disease has come back or has not improved after previous treatment(s) and who have no other satisfactory treatment options.

first and only

Menin inhibitor

First-of-its-kind, FDA-approved,
targeted treatment that works
differently than chemotherapy

Targeted action

Targeted action

Targets menin to disrupt
protein interactions responsible
for driving NPM1m AML

Take it at home

Take it at home

Oral medication with
dosing options for patients
1 year and older

Revuforj® (revumenib) Logo

Revuforj targets and directly binds to menin to help block the source of what can drive your specific type of AML

Targets
Targets
Binds
Binds
Blocks
Blocks

Resources & support

The following tools and resources are designed to help you stay informed and feel supported as you or your loved one begins treatment with Revuforj. No matter where you are on your journey, support can go a long way. Don’t be afraid to reach out for help. Remember, you and your loved one are not alone.

Download important resources

Instructions for Use video

If you are unable to swallow tablets, Revuforj can be crushed and dispersed in water as directed in the Instructions for Use

Demonstration Video

The information provided here is not a substitute for talking with your healthcare provider.
Your healthcare provider is the best source of information about your disease.

Revuforj® (revumenib) Targeted Action

Reach out to your healthcare provider about next steps and ask about getting a starter kit for Revuforj

SyndAccess® Patient Support Program

Eligible commercially insured patients can apply for copay support through the Revuforj® (revumenib) Copay Program.*

Talk with your healthcare team to learn how to enroll in the program.

SyndAccess Patient Support Logo
SyndAccess.com
1-888-567-SYND (7963)

*All programs subject to eligibility criteria and terms and conditions for enrollment.

Important Safety Information

What is the most important information I should know about Revuforj?

Revuforj may cause serious side effects, including:
Differentiation syndrome. Differentiation syndrome is a serious but common condition that affects your blood cells, which may be life-threatening or lead to death if not treated. Differentiation syndrome has happened as early as 3 days and up to 41 days after starting Revuforj. Tell any healthcare provider caring for you that you are taking a medicine that can cause differentiation syndrome. Call your healthcare provider or go to the nearest hospital emergency room right away if you develop any of the following symptoms of differentiation syndrome while taking Revuforj:

  • fever
  • cough
  • shortness of breath
  • severe headache
  • confusion
  • dizziness or lightheadedness
  • fast weight gain
  • swelling of arms, legs, neck, groin, or underarm area
  • decreased urination
  • rash

If you develop any of these symptoms of differentiation syndrome, your healthcare provider may start you on a medicine given through a vein (intravenous) called corticosteroids and may monitor you in the hospital.

Changes in electrical activity of your heart called QT prolongation. QT prolongation is a serious but common side effect that can cause irregular heartbeats that can be life-threatening, such as a heart attack, and can lead to death. Your healthcare provider will check the electrical activity of your heart with a test called an electrocardiogram (ECG) and will also do blood tests to check your potassium and magnesium levels before and during treatment with Revuforj. Tell your healthcare provider right away if you feel faint, lightheaded, dizzy, or if you feel your heart beating irregularly or fast during treatment with Revuforj.

Before taking Revuforj, tell your healthcare provider about all your medical conditions, including if you:
  • have any heart problems, including a condition called long QT syndrome
  • have been told you have low blood levels of potassium or magnesium
  • are pregnant or plan to become pregnant. Revuforj can harm your unborn baby
    Females who are able to become pregnant

    • Your healthcare provider will perform a pregnancy test within 7 days before you start treatment with Revuforj
    • Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with Revuforj
    • Use effective birth control (contraception) during treatment with Revuforj and for 4 months after the last dose of Revuforj

    Males who have female partners who are able to become pregnant

    • Use effective birth control during treatment with Revuforj and for 4 months after the last dose of Revuforj
    • Talk to your healthcare provider about birth control methods you can use during this time
  • Revuforj may cause fertility problems in females and males, which may affect your ability to have children. Talk to your healthcare provider if this is a concern for you
  • are breastfeeding or plan to breastfeed. It is not known if Revuforj passes into your breast milk. Do not breastfeed during your treatment with Revuforj or for 1 week after your last dose of Revuforj

Tell your healthcare provider about all the medications you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Revuforj and other medicines may affect each other, causing side effects.

The most common side effects of Revuforj include:

  • infections, including bacterial and viral
  • changes in liver function tests
  • bleeding (hemorrhage)
  • nausea and vomiting
  • muscle pain
  • low white blood cell counts with fever
  • diarrhea
  • tiredness
  • swelling in the arms and legs
  • decreased appetite
  • constipation

Your healthcare provider may change your dose, temporarily stop, or permanently stop treatment with Revuforj if you develop certain side effects. These are not all the possible side effects of Revuforj. Call your healthcare provider for medical advice about side effects.

You are encouraged to report side effects of prescription drugs to FDA.
Visit www.fda.gov/medwatch or call 1-800-FDA-1088
.

What is Revuforj?

Revuforj® (revumenib) is a prescription medicine used to treat adults and children 1 year and older with:

  • acute leukemia with a lysine methyltransferase 2A gene (KMT2A) translocation whose disease has come back or has not improved after previous treatment(s)
  • acute myeloid leukemia with a nucleophosmin 1 (NPM1) mutation whose disease has come back or has not improved after previous treatment(s) and who have no other satisfactory treatment options

Please see Full Prescribing Information, including BOXED WARNINGS, and Medication Guide and Instructions for Use.

Important Safety Information

What is the most important information I should know about Revuforj?

Revuforj may cause serious side effects, including:
Differentiation syndrome: Differentiation syndrome is a serious but common condition that affects your blood cells, which may be life-threatening or lead to death if not treated. Differentiation syndrome has happened as early as 3