Support throughout the journey
Whether you are considering BEQVEZ or have been prescribed BEQVEZ already, Pfizer is committed to supporting you
†Pfizer PALs are not measured or awarded based on sales performance nor will they ask you to switch products.
While confirming eligibility, consider enrolling in an educational support program called Pfizer GeneTogetherTM
Pfizer GeneTogether is here to help answer your coverage and logistics questions throughout your BEQVEZ journey. If you and your doctor decide BEQVEZ is the right treatment choice for you, your care team will work with you to enroll you in Pfizer GeneTogether.
Learn more
The program includes access to dedicated Patient Case Managers (PCMs), who will be ready to answer any questions you may have about the planning needed to receive BEQVEZ. PCMs will give patients a welcome call and:
- outline potential support options available
- help eligible, commercially insured patients with potential financial assistance
- explain insurance coverage and out-of-pocket costs for gene therapy
Your Pfizer GeneTogether care team will also help you get ready for your infusion by:
- supplying you with information and resources to support you before, during, and after treatment
- assisting you with travel and other logistical details required for your treatment
- confirming the date of the infusion and any preparation or planning needed beforehand
- checking with your care team to make sure you’re all set for your infusion
Learn about other helpful resources available throughout your journey on the Support page
Find more support in your local community
Reaching out to your hemophilia community may help you find more support and resources
These websites are neither owned nor controlled by Pfizer. Pfizer does not endorse and is not responsible for the content or services of these sites.
The National Bleeding Disorders Foundation (formerly the National Hemophilia Foundation) is dedicated to finding cures for inheritable blood and bleeding disorders and to addressing and preventing the complications of these disorders through research, education, and advocacy enabling people and families to thrive.
The Coalition for Hemophilia B strives to make quality of life the focal point of treatment for people with hemophilia B and their families through education, empowerment, advocacy, and outreach.
The Hemophilia Federation of America is a patient advocacy organization serving the rare bleeding disorders community. It advocates for safe and effective therapies and quality, affordable health coverage. Ultimately, it seeks a better quality of life for all persons with bleeding disorders.
