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| FREHEMGO® (denecimig-mima) injection is a prescription medicine that is used to prevent or reduce the number of bleeding episodes in adults and children with hemophilia A with or without Factor 8 inhibitors. |
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| Go for a new subcutaneous option |
| GO FOR FREHEMGO®! |
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| Now FDA approved for people living with hemophilia A with or without inhibitors, FREHEMGO® is a Factor 8a mimetic (nonfactor therapy that acts like Factor 8a) that provides up to a full month of bleed protection in a single-use, prefilled pen.a |
| Want to learn more? |
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Let’s go!
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| aAlso available as once-every-2-week and once-weekly dosing. |
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| Important Safety Information for FREHEMGO® |
| What is the most important information I should know about FREHEMGO®? |
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| Please click here or scroll below for additional Important Safety Information. |
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Achieved thrombin generation
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Designed to generate thrombin in the normal range when needed |
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Factor 8 equivalence of 42% was achieved in lab tests using plasma from people with hemophilia Ab |
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b42% Factor 8 equivalence is a laboratory estimate. In this test, FREHEMGO® produced a peak amount of thrombin similar to that produced by a plasma sample with 42% Factor 8 activity. This does not mean FREHEMGO® contains Factor 8 or raises a person’s Factor 8 level to 42%. FREHEMGO® does not treat bleeds. Make sure you have backup Factor 8 or a bypassing agent in case of a bleed.
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Up to a full month of proven bleed protection
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A single monthly dose helps prevent bleeds before they start |
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Available as once-monthly, once-every-2-week, or once-weekly dosing |
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Quick administration
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Single-use, prefilled pen for subcutaneous administration |
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Patients injected less than 1 mL in less than 1 minute, in a studyc |
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Store at room temperature (up to 86 °F) for up to 2 weeks |
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| cBased on a study in 64 people with hemophilia A with or without inhibitors on Hemlibra® and 11 caregivers who administer Hemlibra®. Study outcomes: to determine if the FREHEMGO® pen is easy to learn how to use and easy to use via nurse training and a simulated injection, and to compare preference with the users’ current drug delivery system. Device training time, preparation/injection time, and number of injections were assessed. |
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| Want the full download on FREHEMGO®? |
| Start a convo with your Rare Blood Community Liaison (RBCL)! |
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Get connected
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| Living with a bleeding disorder can be tough. We get it. That’s why we’ve pulled together a team that can help, starting with your local RBCL. Active in the hemophilia community, they’re ready to provide you with one-on-one support, including: |
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Information about FREHEMGO® |
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Disease and lifestyle education |
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Info on local events |
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Tools to help you manage your bleeding disorder |
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| What is FREHEMGO® |
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| Important Safety Information (cont’d) |
| What is the most important information I should know about FREHEMGO®? (cont'd) |
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| Please click here for Prescribing Information. |
| FREHEMGO® is a prescription medication. |
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088. |
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| Please do not respond to this email. If you would like to contact us, please click here or call 1‑877‑744‑2579. |
| UNSUBSCRIBE NOTICE |
| If you no longer want to receive communications from Novo Nordisk, click here to unsubscribe. You also may call us at 1‑877‑744‑2579 or send us a letter that includes your full contact information (eg, name, email address, phone) to Novo Nordisk, 800 Scudders Mill Road, Plainsboro, New Jersey 08536. To better understand how Novo Nordisk values your privacy, see our Privacy Statement. |
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FREHEMGO® is a registered trademark of Novo Nordisk Health Care AG. Novo Nordisk is a registered trademark of Novo Nordisk A/S. All other trademarks, registered or unregistered, are the property of their respective owners. © 2026 Novo Nordisk All rights reserved. US26DENE00017 October 2026 |
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