Savolitinib is characterized by precise targeting, definite clinical benefits, and manageable safety profile.
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Privacy On June 22, 2021, Savolitinib was first approved by the National Medical
Products Administration (NMPA) of China, indicated for the treatment of patients
with MET exon 14 skipping mutation-positive locally advanced or metastatic
non-small cell lung cancer (NSCLC) who have experienced disease progression
after systemic therapy or are unable to receive chemotherapy.
On March 1, 2023, Savolitinib was included in the National Reimbursement Drug
List (NRDL). It became the only MET-targeted agent successfully incorporated
into the NRDL through medical insurance negotiation, which significantly
improved patient access to the medication.
On January 13, 2025, Savolitinib received further approval from China’s NMPA,
expanding its indication from pretreated patients only to cover both
treatment-naive and pretreated adult patients with MET exon 14 skipping
mutation-positive locally advanced or metastatic NSCLC.
Shanghai, China, 14 January 2025 – AstraZeneca today announced that the National Medical Products Administration (NMPA) of China has officially approv···【Read More】
Update: 26 Jan,2026Source: Haiou HealthViews: 101
On June 23, 2021, the National Medical Products Administration (NMPA) announced the conditional approval of Savolitinib Tablets (trade name: ORPATHYS)···【Read More】
Update: 26 Jan,2026Source: Haiou HealthViews: 95
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