Sickle Cell Disease (SCD), is a rare genetic disorder characterized by expression of abnormal sickle hemoglobin, which leads to a variety of acute and chronic complications. Real-world evidence (RWE) is critical to improve clinical management, reducing healthcare costs, and addressing gaps in care.

We invite you to test the following research objectives with us:

    • Epidemiology and patient characteristics
    • Clinical complications

    • Treatment patterns

    • Healthcare utilization and costs

    • Safety outcomes

We invite you to put our data to the test. E-mail us at contact@lumanity.com to discuss your research needs.

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