发布时间: 2026 - 03 - 05
The year 2026 marks the beginning of the 15th Five-Year Plan period. Recently, the 11th batch of the “Outstanding Domestic Medical Equipment Product Catalogue” was officially released. Viestar’s independently developed BIOPSEE® Confocal Laser Endomicroscope and BIOPSEE® Ultra-Thin Probe-based Confocal Laser Endomicroscope were prominently selected. This recognition makes JWS Medical the exclusive selected product in the confocal microscopy field for this batch, securing a “strong start” for the 15th Five-Year Plan with national-level authoritative certification. This achievement lays...
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发布时间: 2026 - 02 - 27
Preface:Spring breezes blow strong as we spur our horses forward. Riding the momentum of the 2026 Spring Festival (Year of the Horse), Efung Capital received a series of good news this month: Insight Lifetech successfully listed on the Sci-Tech Innovation Board (STAR Market); three portfolio companies simultaneously advanced their Hong Kong IPOs, with all applications accepted for review.Meanwhile, more portfolio companies have achieved multi-point breakthroughs and advanced together in key sectors, writing a new chapter for China's biopharmaceutical industry with vigorous momentum.&#...
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发布时间: 2026 - 02 - 25
Dashi Pharmaceuticals (Guangdong) Co., Ltd. (“Dashi Pharmaceuticals”) today announced that it has entered into an exclusive licensing agreement with Slate Medicines, Inc., a U.S.-based biopharmaceutical company. Under the agreement, Slate Medicines will obtain the exclusive global rights (excluding Greater China) for the clinical development and commercialization of DS009 (to be named SLTE-1009 by Slate Medicines), a potentially best-in-class anti-pituitary adenylate cyclase-activating polypeptide (PACAP) monoclonal antibody independently developed by Dashan Pharmaceuticals. This antibody is i...
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发布时间: 2026 - 02 - 10
On February 9, the CDE website indicated that Trinmab’s Retavibart (TNM001) has been submitted for marketing approval for the prevention of lower respiratory tract infections (LRTI) caused by respiratory syncytial virus (RSV) in infants up to one year of age, including those at high risk for severe RSV infection. This is the second domestic RSV antibody to be considered for priority review, following Ruiyang Pharmaceutical’s Clesrovimab, which was granted priority review just last month.Retavibart is a fully human monoclonal antibody that targets a highly conserved epitope on the pre-fusion (P...
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