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ALPROLIX® has a decade of experience your patients can trust1


Since its approval in 20141,2:

More than 1400 patients

have been prescribed ALPROLIX*

1 billion+ units shipped

More than 1 billion units

of ALPROLIX have been shipped across the country

*Based on specialty pharmacy dispensing records, specialty pharmacy distributor shipment records, third-party logistics’ shipment records, and internal retention estimates from May 2014 through June 2022.2

Units include those that have been shipped to patients from May 2014 through June 2022 and do not include inventory at specialty pharmacy providers or specialty distributors.2

Hear from real patients taking ALPROLIX

Meet Brian

A father and hiker with severe hemophilia B.

Brian transitioned from on-demand to prophylaxis with ALPROLIX.

Meet Alex

A youth soccer coach with moderate hemophilia B.

Alex was able to extend his dosing interval with ALPROLIX.

Meet Erica

Meet Mark

Patient stories reflect the real-life experiences of persons diagnosed with hemophilia who have been prescribed ALPROLIX. However, individual experiences may vary. Patient stories are not necessarily representative of what another person using ALPROLIX may experience. Patients have been compensated for sharing their stories.

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Indication

ALPROLIX is a recombinant DNA derived, coagulation Factor IX concentrate indicated in adults and children with hemophilia B for:

  • On-demand treatment and control of bleeding episodes
  • Perioperative management of bleeding
  • Routine prophylaxis to reduce the frequency of bleeding episodes

Limitation of Use

ALPROLIX is not indicated for induction of immune tolerance in patients with hemophilia B.

Important Safety Information

Contraindication

ALPROLIX is contraindicated in patients who have a known history of hypersensitivity reactions, including anaphylaxis, to the product or its excipients.

Warnings and Precautions

  • Allergic-type hypersensitivity reactions, including anaphylaxis, are possible with factor replacement therapies, and have been reported with ALPROLIX. Discontinue use of ALPROLIX if hypersensitivity symptoms occur, and initiate appropriate treatment.
  • Formation of neutralizing antibodies (inhibitors) to Factor IX has been reported following administration of ALPROLIX. Patients using ALPROLIX should be monitored for the development of Factor IX inhibitors. Clotting assays (e.g., one-stage) may be used to confirm that adequate Factor IX levels have been achieved and maintained.
  • The use of Factor IX products has been associated with the development of thromboembolic complications.
  • Nephrotic syndrome has been reported following attempted immune tolerance induction in hemophilia B patients with Factor IX inhibitors and a history of allergic reactions to Factor IX. The safety and efficacy of using ALPROLIX for immune tolerance induction have not been established.

Adverse reactions

The most common adverse reactions (incidence ≥1%) in previously untreated patients were injection site erythema, hypersensitivity, and Factor IX inhibition. The most common adverse reactions (incidence ≥1%) in previously treated patients were headache, oral paresthesia, and obstructive uropathy.

Indication

Important Safety Information

References: 1. ALPROLIX [package insert]. Waltham, MA: Bioverativ Therapeutics Inc. 2. Data on file. Waltham, MA; Bioverativ Therapeutics Inc.

©2024 Sanofi. All rights reserved. ALPROLIX and Sanofi are registered trademarks of Sanofi or an affiliate. All other trademarks are the property of their respective owners. MAT-US-2021405-v7.0-09/2024 Last updated: September 2024