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Expert Q&A: Gene-Editing Treatment for Sickle Cell Disease May Be Out of Reach for Many

December 8, 2023

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Read time:

<5 mins
Sickle Cells Blood Vessels 0

Newly approved by the FDA, CRISPR-based Exa-cel gene editing technology can potentially treat thousands of patients with sickle cell disease. However, this new therapy is expensive and intense and, to start will only be offered by a few healthcare providers. In this Q&A with the Institute for Healthcare Policy and Innovation, Melissa Creary, Ph.D., an assistant professor of health management policy and global public health at U-M’s School of Public Health and a person living with sickle cell, brings her perspective to the conversation about the accessibility of this breakthrough treatment.

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