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Takeda and Fudan University's IMI Launch AI-Based Rare Disease Screening and Diagnosis Project
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Takeda and Fudan University’s IMI Launch AI-Based Rare Disease Screening and Diagnosis Project

LinkedCare Raises Hundreds of Millions in Series E Funding Led by State-Owned Investors
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LinkedCare Raises Hundreds of Millions in Series E Funding Led by State-Owned Investors

Grand Life Sciences Partners with Cali Biosciences for CPL-01 Commercialization in China
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Grand Life Sciences Partners with Cali Biosciences for CPL-01 Commercialization in China

Insilico Medicine's ISM5411 Shows Positive Results in Phase I Studies for Inflammatory Bowel Disease
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Insilico Medicine’s ISM5411 Shows Positive Results in Phase I Studies for Inflammatory Bowel Disease

GlycoNex Licenses SPD8 Biosimilar to Undisclosed Company for Osteoporosis Treatment
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GlycoNex Licenses SPD8 Biosimilar to Undisclosed Company for Osteoporosis Treatment

Yiling Pharmaceutical Withdraws Clinical Filing for G201-Na in Assisted Reproduction
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Yiling Pharmaceutical Withdraws Clinical Filing for G201-Na in Assisted Reproduction

China-based Dizal Pharmaceutical Co., Ltd (SHEX: 688192) has announced that its New Drug Application (NDA) for sunvozertinib has been accepted for review by the US FDA with priority review status. The EGFR inhibitor is targeting approval to treat locally advanced or metastatic non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) exon 20 insertion mutations (exon20ins), as detected by an FDA-approved test, whose disease has progressed on or after platinum-based chemotherapy.
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Dizal’s Sunvozertinib Receives Priority Review from FDA for EGFR Exon 20 NSCLC

Boehringer Ingelheim and Sutro Achieve Commercial-Scale Manufacturing of Luvelta
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Boehringer Ingelheim and Sutro Achieve Commercial-Scale Manufacturing of Luvelta

Variant Bio Partners with Novo Nordisk to Discover Novel Targets for Metabolic Diseases
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Variant Bio Partners with Novo Nordisk to Discover Novel Targets for Metabolic Diseases

AbbVie Exercises Option for Capsida's Neurodegenerative Disease Program
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AbbVie Exercises Option for Capsida’s Neurodegenerative Disease Program

Eyebright Medical's Loong Crystal PR Receives NMPA Class III Medical Device Approval
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Eyebright Medical’s Loong Crystal PR Receives NMPA Class III Medical Device Approval

CSPC Pharmaceutical Group Receives NMPA Approvals for ADC SYS6045 and PDE4B Inhibitor SYH2059
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CSPC Pharmaceutical Group Receives NMPA Approvals for ADC SYS6045 and PDE4B Inhibitor SYH2059