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| Indicated for use in adults and children with hemophilia B for on-demand treatment and control of bleeding episodes, perioperative management of bleeding, and routine prophylaxis to reduce the frequency of bleeding episodes. See Limitations of Use below. |
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| were observed in patients who switched to Rebinyn®1 |
| In a retrospective, observational, real-world study of 42 patients, fewer bleeds were observed in patients who switched to Rebinyn®1,a |
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| Data from the Canadian Bleeding Disorders Registry |
| Low annualized bleeding rate (ABR) with Rebinyn® prophylaxis |
Mean intrapatient ABR when switching
from BeneFIX® to Rebinyn® prophylaxis1,a |
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Mean intrapatient ABR when switching
from Alprolix® to Rebinyn® prophylaxis1,a |
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| aBased on a retrospective, observational, real-world study of 42 patients with hemophilia B (5 patients were <18 years old) that switched from either BeneFIX® or Alprolix® prophylaxis to Rebinyn® prophylaxis using published Canadian Bleeding Disorders Registry (CBDR) data. Patients had to be on a previous therapy for at least 6 months and have at least 6 months of follow-up with Rebinyn®. CBDR formulary mandated a switch from Alprolix® to Rebinyn®, and patients had the option to switch from BeneFIX® to Rebinyn®.1 |
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| Scroll down to view prophylaxis pivotal trial efficacy data. |
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| Selected Important Safety Information |
| Contraindications |
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Rebinyn® is contraindicated in patients with a known hypersensitivity to Rebinyn® or its components, including hamster proteins. |
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| Warnings and Precautions |
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Hypersensitivity Reactions: Allergic-type hypersensitivity reactions, including anaphylaxis, have occurred with Rebinyn®. Signs may include angioedema, chest tightness, difficulty breathing, wheezing, urticaria, and itching. Discontinue Rebinyn® if allergic- or anaphylactic-type reactions occur and initiate appropriate treatment. |
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| Please click here or scroll below for additional Important Safety Information. |
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| Rebinyn® prophylaxis treatment helps stop bleeds before they start.2 |
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| Keep up with important information about treatments for rare bleeding disorders. |
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| Indications and Usage |
| Rebinyn®, Coagulation Factor IX (Recombinant), GlycoPEGylated, is a recombinant DNA derived coagulation Factor IX concentrate indicated for use in adults and children with hemophilia B (congenital Factor IX deficiency) for on demand treatment and control of bleeding episodes, perioperative management of bleeding, and routine prophylaxis to reduce the frequency of bleeding episodes. |
| Limitations of Use: Rebinyn® is not indicated for immune tolerance induction in patients with hemophilia B. |
| Important Safety Information (cont’d) |
| Warnings and Precautions |
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Inhibitors: The formation of inhibitors (neutralizing antibodies) to Factor IX has occurred following Rebinyn®. If expected plasma factor IX activity levels are not attained, or if bleeding is not controlled as expected with the administered dose, perform an assay that measures Factor IX inhibitor concentration. Monitor all patients using clinical observations and laboratory tests for the development of inhibitors. Factor IX activity assay results may vary with the type of activated partial thromboplastin time reagent used. |
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Thrombotic Events: The use of Factor IX-containing products has been associated with thromboembolic complications. Monitor for thrombotic and consumptive coagulopathy when administering Rebinyn® to patients with liver disease, post-operatively, to newborn infants, or to patients at risk of thrombosis or disseminated intravascular coagulation (DIC). |
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Nephrotic Syndrome: Nephrotic syndrome has been reported following immune tolerance induction therapy with Factor IX products in hemophilia B patients with Factor IX inhibitors, often with a history of allergic reactions to Factor IX. The safety and efficacy of using Rebinyn® for immune tolerance induction have not been established. |
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| Adverse Reactions |
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The most common adverse reactions reported in previously treated patients in clinical trials (≥1%) were itching and injection site reactions. The most common adverse reactions (≥1%) in previously untreated patients reported in clinical trials were rash, FIX inhibitors, hypersensitivity, itching, injection site reaction, and anaphylactic reaction. |
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Animals administered Rebinyn® showed accumulation of PEG in the choroid plexus, pituitary, circumventricular organs, and cranial motor neurons. The potential clinical implications of these animal findings are unknown. Consider whether the patient is vulnerable to cognitive impairment, such as infants and children who have developing brains, and patients who are cognitively impaired. |
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| Please click here for Prescribing Information. |
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| 1. |
Matino D, Iorio A, Keepanasseril A, et al. Switching to nonacog beta pegol in hemophilia B: outcomes from a Canadian real-world, multicenter, retrospective study. Res Pract Thromb Haemost. 2022;6(3):e12661. |
| 2. |
Young G, Collins PW, Colberg T, et al. Nonacog beta pegaol (N9-GP) in haemophilia B: a multinational phase III safety and efficacy extension trial (paradigmtm 4). Thromb Res. 2016;141:69-76 |
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