With the recent Hemlibra approval and the gene therapy revolution, we are seeing a much-needed race to innovate more effective, long-lasting and curative therapies for hemophilia and acquired bleeding disorders.

As such, the 3rd Hemophilia Drug Development Summit is going digital and remains dedicated to bringing to patients more effective commercially and clinically translated therapies from small molecules to gene therapies to improve patients’ quality of life.

Bringing together over 100 of the world’s leading experts and drug developers, we discuss how to develop new therapies for a responsive subset of hemophiliac patients, optimize clinical trial development (setup and management) and discuss the patient/payer paradigm to ensure these novel therapies are affordable and accessible.

Brought direct to your home office with a jam packed agenda and online virtual networking opportunities, this exclusive virtual summit will delve into the challenges of treating each patient subset, as well as hearing the latest advancements in gene therapy and discussing the critical hurdles that need to be overcome to meet the unmet clinical need of all patients.

Join us as we unite drug developers and researchers on a dedicated online platform and look to the innovation driving the field towards more long-acting and curative therapies to improve patient quality of life.

To know more about Hemophilia Drug Development Summit please click here.