Patients request Leqembi¡¯s reimb even before approval
By Eo, Yun-Ho | translator Kang, Shin-Kook
24.04.29 05:55:19
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final stages of market authorization review underway by MFDS
Biogen applied for US FDA approval of Leqembi¡¯s monthly intravenous injection formulation
Leqembi has been proven to reduce the rate of disease progression and slow cognitive decline by selectively binding to amyloid beta (A¥â) aggregates, which are a known cause of Alzheimer's disease.
Due to such a lack of treatments for the disease, the desperation of the patients and their families has been indescribable. In addition to public petitions, the MFDS's Korea Orphan & Essential Drug Center has been inundated with inquiries on the date of Leqembi¡¯s approval and supply in Korea.
However, the problem is the pri
Eo, Yun-Ho(unkindfish@dailypharm.com)
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