- Overview
- Activity Format & Credit
- Meet the Panel
- Register Here
- Overview
-
More
- Activity Format & Credit
- Meet the Panel
- Register Here
STATEMENT OF NEED
Hemophilia is an inherited coagulation disorder defined by spontaneous or traumatic bleeding which significantly impacts patient quality of life. The emergence of new therapies, including extended half-life clotting factor concentrates, factor VIII mimetics, rebalancing agents, and gene therapies, has expanded the treatment landscape and transformed patient outcomes. However, the complexity of treatment selection and gaps in guideline recommendations leave many unanswered questions for clinicians seeking to optimize care for their patients (Young et al, 2025; Lewandowska et al, 2025). This Panel Discussion, presented as a Friday Satellite Symposium at the 67th American Society of Hematology (ASH) Annual Meeting, will explore approaches for filling in the gaps in hemophilia guideline recommendations with evidence-based strategies to optimize patient-relevant outcomes. The Panel will feature expert perspectives from Lynn Malec, MD, MSc; Allison P. Wheeler, MD, MSCI; Shannon L. Meeks, MD, MBA; Michael Recht, MD, PhD; and Annette von Drygalski, MD, PharmD, RMSK.
TARGET AUDIENCE
Hematologists, hematology advanced practitioners, and other healthcare professionals involved in the care of patients with hemophilia.
LEARNING OBJECTIVES
Upon completion of this activity, participants should be able to:
- Define appropriate treatment goals and targets for the management of hemophilia A and B
- Determine which patients with hemophilia A and B should be prescribed prophylaxis
- Compare safety, efficacy, and therapeutic selection considerations for prophylactic agents in the treatment of patients with hemophilia A and B
- Evaluate strategies to tailor hemophilia prophylaxis to patients’ needs
REGISTRATION
JOINTLY ACCREDITED PROVIDER
In support of improving patient care, i3 Health is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
PHYSICIANS
i3 Health designates this live activity for a maximum of 2.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 2.5 Medical Knowledge MOC points in the American Board of Internal Medicine’s (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider’s responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit.
By providing this information, participants are agreeing to allow i3 Health to share this information with the ACCME.
Physician Assistants/Associates
i3 Health has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with AAPA CME Criteria. This activity is designated for 2.5 AAPA Category 1 CME credits. Approval is valid until 12/5/25. PAs should only claim credit commensurate with the extent of their participation.
Nurse Practitioners
The American Academy of Nurse Practitioners Certification Program (AANPCP) accepts AMA PRA Category 1 Credit™ from organizations accredited by the ACCME. Individuals are responsible for checking with the AANPCP for further guidelines.
DISCLOSURE OF RELEVANT FINANCIAL INFORMATION WITH INELIGIBLE COMPANIES
i3 Health endorses the standards of the ACCME that require everyone in a position to control the content of a CME activity to disclose all financial relationships with ineligible companies that are related to the content of the CME activity. CME activities must be balanced, independent of commercial bias, and promote improvements or quality in health care. All recommendations involving clinical medicine must be based on evidence accepted within the medical profession.
A conflict of interest is created when an individual has an opportunity to affect CME content about products or services of an ineligible company with which he/she has a financial relationship, which therefore may bias their opinions and teaching. This may include receiving a salary, royalty, intellectual property rights, consulting fee, honoraria, stocks, or other financial benefits.
i3 Health will identify, review, and mitigate all relevant financial relationships that speakers, authors, or planners disclose prior to an educational activity being delivered to learners. Disclosure of a relationship is not intended to suggest or condone bias in any presentation but is made to provide participants with information that might be of potential importance to their evaluation of a presentation. i3 Health does not endorse any products or services.
Relevant financial relationships exist between the following individuals and ineligible companies:
Lynn Malec, MD, MSc - TBD
Allison P. Wheeler, MD, MSCI, discloses that she has served on an advisory board or panel for Bayer, Cerus, CSL Behring, Hemab, Novo Nordisk, Octapharma, Pfizer, Sanofi, SeraGene, and Vega; and that she has received grants/research support from Octapharma.
Shannon L. Meeks, MD, MBA - TBD
Michael Recht, MD, has no relevant financial relationships to disclose.
Annette von Drygalski, MD, PharmD, RMSK - TBD
The i3 Health planners, reviewers, and managers have nothing to disclose.
i3 Health has mitigated all relevant financial relationships.
INSTRUCTIONS TO RECEIVE CREDIT
In order to receive credit for this activity, participants must submit a completed evaluation at the end of the activity.
TECHNOLOGY REQUIREMENTS FOR VIRTUAL CME | NCPD | CPE ACTIVITIES
For virtual (asynchronous, archived live, home study; synchronous webinars) CME/NCPD/CPE activities, include access to system requirements:
- The Internet browser(s) supported and minimum versions of each required by the learner to complete the online activity.
- The minimum memory, storage, processor, and Internet speeds require by the learner to complete the online activity.
UNAPPROVED USE DISCLOSURE
i3 Health requires CME faculty (speakers) to disclose to attendees when products or procedures being discussed are off-label, unlabeled, experimental, and/or investigational (not FDA approved), as well as any limitations on the information that is presented, such as data that are preliminary or that represent ongoing research, interim analyses, and/or unsupported opinion. Faculty may discuss information about pharmaceutical agents that is outside of U.S. Food and Drug Administration approved labeling.
This information is intended solely for continuing medical education and is not intended to promote off-label use of these medications. If you have questions, contact the medical affairs department of the manufacturer for the most recent prescribing information.
DISCLAIMER
The information provided at this CME activity is for continuing education purposes only and is not meant to substitute for the independent medical/clinical judgment of a healthcare provider relative to diagnostic and treatment options of a specific patient’s medical condition.
COMMERCIAL SUPPORT
This educational activity is supported by an independent medical education grant from Sanofi.
Aggregate participant data will be shared with commercial supporters of this activity.
CONTACT INFORMATION
Technical queries or questions regarding activity credit should be directed to i3 Health at support@i3health.com.
FORMAT
Live Symposium
CREDIT
2.5 AMA PRA Category 1 Credits™
2.5 AAPA Category 1 CME credits
ESTIMATED TIME TO COMPLETE
2.5 hours
DATE AND LOCATION INFORMATION
ASH Annual Meeting - Friday Satellite Symposium
Orange County Convention Center
9800 International Drive
Orlando, FL 32819
Room: Valencia W415A
December 5, 2025
3:00 pm ET
Lynn Malec, MD, MSc, is the Senior Medical Director of Versiti Medical Sciences Institute and an Associate Professor of Medicine and Pediatrics at the Medical College of Wisconsin. She specializes in the treatment of both adults and children with bleeding and clotting disorders, and her clinical research focuses on understanding inhibitor development and the outcomes of factor replacement strategies in patients with hemophilia.
Allison P. Wheeler, MD, MSCI, is the Scientific Director at the Washington Center for Bleeding Disorders and an Associate Professor at the University of Washington School of Medicine. She specializes in the treatment of hemostatic disorders, and her clinical research focuses on better understanding bleeding disorders in female patients and improving care for this population.
Shannon L. Meeks, MD, MBA, is a Professor of Pediatrics at Emory University and a Pediatric Hematologist/Oncologist at Aflac Cancer and Blood Disorders Center, Children’s Healthcare of Atlanta. Her basic, translational, and clinical research studies the immune response in hemophilia A, with particular focus on characterizing the epitopes recognized in the B-cell response to factor VIII.
Michael Recht, MD, PhD, is a Professor of Clinical Pediatrics at Yale School of Medicine and the Chief Medical and Scientific Officer of the National Bleeding Disorders Foundation. He specializes in the treatment of pediatric and adult patients with bleeding and clotting disorders. He has actively participated in over 110 clinical trials investigating novel therapies for patients with inherited blood disorders, including gene therapy for hemophilia.
Annette von Drygalski, MD, PharmD, RMSK, is a Professor of Medicine and the Director of the Center for Bleeding and Clotting Disorders at the University of California, San Diego. She specializes in the treatment of bleeding and clotting disorders, and she is the institutional leading investigator of several international trials investigating long-acting or novel clotting factor products. Her research also studies hypertension, bone disease, and joint disease in patients with hemophilia.
Hemophilia is an inherited bleeding disorder that significantly impacts patients’ quality of life. With new therapies such as extended half-life clotting factor concentrates, factor VIII mimetics, rebalancing agents, and gene therapies, treatment options have expanded dramatically. Yet, gaps in current guideline recommendations leave many unanswered questions for clinicians working to optimize care.
Join us for a CME-approved Friday Satellite Symposium Panel Discussion, Filling in the Gaps in Hemophilia Guideline Recommendations: Evidence-Based Strategies to Optimize Patient-Relevant Outcomes, to be held at the 67th ASH Annual Meeting on Friday, December 5, from 3:00 pm - 6:00 pm.
This engaging panel will explore:
- Key gaps in hemophilia guideline recommendations
- Evidence-based strategies for treatment selection and sequencing
- Practical insights on integrating novel therapies into care
- Approaches to optimize patient-relevant outcomes
Don’t miss this opportunity to hear expert perspectives and gain actionable strategies to improve hemophilia care.
REGISTER NOW to reserve your spot!
LOCATION INFORMATION:
ASH Annual Meeting - Friday Satellite Symposium
Orange County Convention Center
9800 International Drive
Orlando, FL 32819
Room: Valencia W415A
December 5, 2025
3:00 pm ET - 6:00 pm ET