EADV 2026 data highlight dupilumab’s effects on growth, quality of life, disease control, and itch across multiple dermatologic diseases.
|Articles|June 1, 2001
Drug shortage complaints falling on deaf ears at FDA
Washington - Although physicians, pharmaceutical manufacturers, and hospital officials have met with the FDA to discuss shortages of several anesthetics and other drugs, the federal agency has no plans to have a public hearing on the situation, according to an FDA spokesperson.
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The FDA approved therapies for melanoma, dermatomyositis, superficial basal cell carcinoma, and adolescent alopecia areata, while TYK2 inhibitors and rare disease filings advanced toward 2027 decisions.
Dermatology Times is looking back on the top stories in dermatology from the month of September.
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The FDA approval, based on 36-week data from the phase 3 BRAVE-AA-PEDS trial, extends baricitinib access to patients as young as 12 years old with severe alopecia areata.
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