Financial programs and support for patients
Novo Nordisk provides assistance through NovoCare®, a network to help your patients access co-pay savings, product support, and more.
Financial programs and support for patients
Novo Nordisk provides assistance through NovoCare®, a network to help your patients access co-pay savings, product support, and more.
![Father and son smiling](/rare-bleeding-disorders/products/treatments/esperoct/cost-coverage/_jcr_content/root/slab_1160150279/content/image.img.jpeg/1724785855823/mother-son-smiling.jpeg)
NovoCare® is designed for your patients
Patients can access:
- Product support programs that help with treatment costs
- Representatives who speak Spanish to better serve them
You can help your patients by calling 1‑844‑668‑6732 or have them contact NovoCare® at NovoCare.com
NovoCare® can help with:
QuickCheck™ benefits verification
![Document with green checkmark icon](/rare-bleeding-disorders/products/treatments/esperoct/cost-coverage/_jcr_content/root/slab_636141030/content/container_1821293537/container/image.img.png/1694025914912/document-green-checkmark-icon.png)
Verify your patients' benefits and receive confirmation of coverage. If no coverage is available, names of alternative therapies may be supplied.
Patient Assistance Program (PAP)
![Hand holding a heart icon](/rare-bleeding-disorders/products/treatments/esperoct/cost-coverage/_jcr_content/root/slab_636141030/content/container_1821293537/container_copy/image.img.png/1694025921081/hand-holding-heart-icon.png)
See if your patients are eligible to receive their treatment free of charge. No registration or monthly fees required.
Patient Trial
Program
![Medication bag with a heart icon](/rare-bleeding-disorders/products/treatments/esperoct/cost-coverage/_jcr_content/root/slab_636141030/content/container_1821293537/container_copy_2098003598/image.img.png/1694025927157/medication-bag-heart-icon.png)
Find out if your patients qualify to receive a limited supply of Novo Nordisk's product for free.
Patient
enrollment form
![Form with plus sign icon](/rare-bleeding-disorders/products/treatments/esperoct/cost-coverage/_jcr_content/root/slab_636141030/content/container_1821293537/container_copy_1867868118/image.img.png/1694025934709/form-plus-sign-icon.png)
Download and complete the patient enrollment form to attest your patient's need for treatment.
Interim Product Program
This limited program provides hemophilia therapy to qualifying patients during a coverage gap. Contact a NovoCare® Specialist by calling 1‑844‑668‑6732.
Free Trial Prescription
![Esperoct® vial](/rare-bleeding-disorders/products/treatments/esperoct/cost-coverage/_jcr_content/root/slab_60979772/content/container_2078275516/image.img.png/1724785160893/esperoct-vial.png)
Help your patients make the switch to Esperoct®. Learn more about Novo Nordisk’s trial prescription and support programs. To learn more about our trial prescription program, please call 1‑844‑668‑6732 to speak with a NovoCare® Specialist.
Questions about the NovoCare® program?
Selected Important Safety Information for Esperoct®
Contraindications
- Do not use in patients who have known hypersensitivity to Esperoct® or its components, including hamster proteins
Warnings and Precautions
- Hypersensitivity reactions, including anaphylaxis, may occur. Should hypersensitivity reactions occur, discontinue Esperoct® and administer appropriate treatment
Indications and Usage
Esperoct® [antihemophilic factor (recombinant), glycopegylated-exei] is indicated for use in adults and children with hemophilia A for on-demand treatment and control of bleeding episodes, perioperative management of bleeding, and routine prophylaxis to reduce the frequency of bleeding episodes
- Esperoct® is not indicated for the treatment of von Willebrand disease
Important Safety Information
Contraindications
- Do not use in patients who have known hypersensitivity to Esperoct® or its components, including hamster proteins
Warnings and Precautions
- Hypersensitivity reactions, including anaphylaxis, may occur. Should hypersensitivity reactions occur, discontinue Esperoct® and administer appropriate treatment
- Development of neutralizing antibodies (inhibitors) has occurred. Perform an assay that measures Factor VIII inhibitor concentration if bleeding is not controlled with the recommended dose of Esperoct® or if the expected plasma Factor VIII activity levels are not attained
- Temporary decrease in Factor VIII incremental recovery (IR) has been observed after Esperoct® infusion, within the first 5 exposure days, in previously untreated patients (PUPs) <6 years of age. During the decreased IR period, these subjects may have an increased bleeding tendency. If bleeding is not controlled with the recommended dose of Esperoct® and/or the expected Factor VIII activity levels are not attained and Factor VIII inhibitors are not detected, consider adjusting the dose, dosing frequency, or discontinuing Esperoct®
Adverse Reactions
- The most frequently reported adverse reactions in clinical trials (≥1%) were rash, redness, itching (pruritus), and injection site reactions. Additional frequently reported adverse reactions (≥1%) in PUPs included Factor VIII inhibition and hypersensitivity.
Please click here for Esperoct® Prescribing Information.