HUTCHMED Receives Breakthrough Therapy Designation In China For Fruquintinib Combination With Sintilimab
Portfolio Pulse from Benzinga Newsdesk
HUTCHMED has received Breakthrough Therapy Designation (BTD) from China's National Medical Products Administration for the combination of fruquintinib and sintilimab for the treatment of patients with advanced endometrial cancer. The treatment is specifically for patients with pMMR1 tumors that have failed at least one line of platinum-based therapy.
July 20, 2023 | 5:07 am
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HUTCHMED's new breakthrough therapy designation could potentially boost its market position in China's healthcare sector. This could lead to increased revenues in the future.
The Breakthrough Therapy Designation is a significant regulatory milestone that could potentially expedite the development and review of the drug. This could lead to earlier market entry and increased revenues for HUTCHMED. Furthermore, the designation indicates that the drug could meet an unmet medical need, which could further boost its market position.
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