发布时间: 2025 - 12 - 19
Today, ChinaVenture Information released its "2025 Guangdong-Hong Kong-Macao Greater Bay Area Ranking." Efung Capital was named to ChinaVenture's 2025 Top 30 Best Venture Capital Institutions in the Greater Bay Area.This ranking surveyed nearly 200 equity investment institutions and approximately 60 guidance funds in the Greater Bay Area. Adopting a combination of quantitative and qualitative methodologies, the evaluation assessed selected institutions based on criteria including assets under management, investment activity, and exit performance. The process involved initial scre...
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发布时间: 2025 - 12 - 17
On December 15, 2025, Biostar Pharma, Inc., the U.S. wholly-owned subsidiary of Beijing Huahao Zhongtian Biopharmaceutical Co., Ltd., announced the first patient dosing in its U.S. pivotal registrational clinical study (NCT06764940) evaluating Utidelone injection (UTD1), one of its core product's key overseas clinical pipelines, in combination with capecitabine for HER2-negative breast cancer brain metastases (BCBM).The study adopts a two-stage design and plans to enroll approximately 120 subjects. The primary endpoint is central nervous system objective response rate (CNS-ORR). Nearly 20 ...
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发布时间: 2025 - 12 - 16
On December 16, 2025, Hangzhou Atom Therapeutics Co., Ltd. announced that its Phase II clinical trial application for ABP-745, a small molecule innovative drug in the anti-inflammatory field for the treatment of atherosclerosis, has been approved by the U.S. FDA. The company has initiated a multicenter Phase II clinical trial spanning the United States, China, and Australia, with Academician Ge Junbo, a cardiology expert at Zhongshan Hospital affiliated with Fudan University and an academician of the Chinese Academy of Sciences, serving as the Leading Principal Investigator.Atherosclerosis is ...
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发布时间: 2025 - 12 - 11
Recently, the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) approved Genuine Biotech Co., Ltd.'s GEN-725 tablets (Azvudine) for a Phase IIa clinical trial in the treatment of hematologic malignancies. This approval marks an important step forward in Azvudine's clinical development in the field of hematologic oncology.Azvudine tablets are the first domestically approved nucleoside analog oral anti-HIV drug with independent intellectual property rights. The product has accumulated R&D and safety experience across indications including anti-HI...
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