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Managing the Complex and Differentiated Patient With Hemophilia: Managed Care Considerations in Diagnosis, Treatment Selection, and Unmet Needs

September 28, 2026 | October 14, 2026 | October 19, 2026 | 1:00 PM & 8:00 PM EDTVirtual

Program Description

Hemophilia is a rare, inherited bleeding disorder caused by a deficiency in clotting factor VIII or IX, affecting an estimated 33,000 people in the United States. Aside from potentially life-threatening bleeding episodes, hemophilia drives lifelong risk of joint damage, chronic pain, and diminished quality of life. For decades, factor replacement therapy has been the mainstay of treatment, but a wave of newer nonfactor therapies is reshaping the treatment landscape with novel mechanisms of action and potentially less frequent, subcutaneous dosing options that may improve medication use and quality of life. These advances increase the complexity of decision-making for managed care professionals, as they must weigh evolving clinical trial and real-world evidence, mechanism-specific monitoring needs, and treatment costs when designing formularies, prior authorization criteria, and utilization management strategies. Payers, pharmacy benefit managers, pharmacy directors, and Pharmacy and Therapeutics committee members are increasingly called on to translate this rapidly changing evidence base into coverage decisions that balance patient access with responsible resource allocation. This webinar will equip managed care professionals and pharmacists with an updated understanding of hemophilia pathophysiology, the mechanisms and evidence supporting nonfactor therapies, and practical strategies for building formularies and utilization management approaches that reflect current clinical guidance.

Target audience: Managed  Care Pharmacists
Type of activity: Application
Release date: September 28, 2026
Expiration date: December 19, 2026
Time to complete activity: 1 hour
Learner level: Foundational, Intermediate
Fee: Free

Educational Objectives

At the completion of this activity, participants will be able to:

  • Ascertain the disease pathology in hemophilia, variability in disease presentation, and ongoing patient burden of disease
  • Interpret clinical trial and real-world evidence for nonfactor therapies and their mechanisms of action compared with traditional factor replacement therapies
  • Construct formularies and drug utilization management strategies that align with clinical trial evidence and support improved outcomes for patients with hemophilia

Supported by an educational grant from Genentech, a member of the Roche Group.

What's Included
  • Access your activities anytime, anywhere, with a computer, tablet or smartphone
  • Free access with a PTCE account
  • Pharmacy education designed to improve patient care

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