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Nanjing Sanhome’s Oritinib Ships Widely for EGFR-mutated NSCLC Treatment in China
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Nanjing Sanhome Pharmaceutical Co., Ltd, a notable player in the pharmaceutical sector, has announced the widespread distribution of its Category 1 chemical drug, oritinib, across key regions in China, including Jiangsu, Shanghai, Beijing, Henan, and Inner Mongolia. The drug has been made available to lung cancer specialists who are now…
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Nanjing Sanhome Pharmaceutical and China Resource Pharma Deepen Collaboration for Market Expansion
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Nanjing Sanhome Pharmaceutical Co., Ltd, a Chinese pharmaceutical company, and China Resource Pharmaceutical Commercial Group have been engaged in extensive business discussions across various locations in China, including Tianjin, Chengdu, Hebei, Shanghai, and Shanxi, with the strategic goal of expanding their market presence. The collaboration between the two entities focuses…
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Nanjing Sanhome’s Oritinib Wins NMPA Approval for EGFR T790M Positive NSCLC
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Nanjing Sanhome Pharmaceutical Co., Ltd has received approval from the National Medical Products Administration (NMPA) for its Category 1 chemical drug oritinib, indicated for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) positive for EGFR T790M mutation in patients who have confirmed disease progression during or…
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SMPA Suspends Procurement of Levornidazole by Warrant Pharmaceutical Over IP Concerns
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Shanghai’s Sunshine Medical Procurement All-in-One (SMPA) has released a notification to suspend the procurement status of two levornidazole specifications manufactured by Hunan Warrant Pharmaceutical Co., Ltd (SHA: 688799), citing the need for intellectual property (IP) protection. Additionally, Anhui province has also paused the procurement of two levornidazole specifications made by…
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Betta Pharmaceuticals’ BPI-D0316 Shows Promise in Phase II/III Lung Cancer Study
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China-based Betta Pharmaceuticals Co., Ltd (SHE: 300558) has announced the summary report of a Phase II/III study for its third-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) BPI-D0316. The study evaluated the drug as a first-line treatment for naïve locally advanced or metastatic non-small cell lung cancer (NSCLC) with EGFR…
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Innovent’s Parsaclisib Filed for Marketing Approval in China
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China’s Center for Drug Evaluation (CDE) has received a marketing approval application for Innovent Biologics Inc’s (HKG: 1801) PI3Kδ inhibitor parsaclisib. The product candidate has been granted priority review status. The targeted indication is relapsed or refractory follicular lymphoma (r/r FL) in patients who have previously received at least two…
