Patients deserve immediate access to FDA-approved innovations — not bureaucratic restrictions ...Middle East

Innovation is the lifeblood that has made America the most economically successful nation in the modern era. Biomedical innovation, however, is a costly and risky business. For example, only 5 percent of new cancer compounds make it to patients. Once breakthrough drugs or devices are approved as safe and effective for use by the Food and Drug Administration (FDA) patients — especially those on public health programs — should have immediate access to them. Unfortunately, this is far from the case.  For example, Alzheimer’s patients had high hopes for Aduhelm from Biogen, but the Centers for Medicare & Medicaid Services (CMS) apparently did not trust FDA’s judgment in approving the drug. M

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