Utidelone recommended by “2023 CSCO Guidelines for Diagnosis and Treatment of Breast Cancer” as Class I
2023
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2022
UTD1 Phase 3 INDs approved by NMPA for NSCLC and BC neoadjuvant; UTD2 Phase 1 INDs approved by FDA and NMPA
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2023
Utidelone listed in “China's national reimbursement drug list”
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2022
Biostar Pharma, Inc. (US subsidiary) incorporated
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2021
Extraordinary general meeting held and share-holding reform completed
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2021
Utidelone Injectable NDA approval for the first indication of advanced breast cancer
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2020
Pre-IPO financing of 890 million RMB
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2018
Utidelone Injectable NDA submission as priority review
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2017
Chengdu manufacturing base established for microbial fermentation production and drug product manufacturing
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2016
Utidelone Injectable Phase 3 reached the primary endpoint
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2015
Wholly-owned subsidiary incorporated in Chengdu
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2012
R&D center established covering key biosynthesis platforms
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2011
Utidelone Injectable Phase 2/3 IND approved
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2007
Utidelone injectable Phase 1 IND approved
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2002
Beijing Biostar Pharmaceuticals incorporated in Beijing China
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