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前海开源基金崔宸龙:产业趋势为先 好公司应具备三大标准
Zhong Zheng Wang· 2025-12-18 13:52
他介绍,在界定好公司时,主要关注三个标准:一是拉长时间看,比如未来三到五年,公司所在行业上 行趋势较为明确,发展空间较大;二是公司拥有较深厚的产品或技术积累,"护城河"足够深,核心竞争 力较为明显,能够在相对长一段时间里不被同行所超越,且其竞争优势是可以被上下游产业链所印证 的;三是公司愿意保持较高的研发投入、持续的创新能力,以及实现产品引领行业发展、代表行业创新 的方向。 中证报中证网讯(记者张韵)12月18日晚间,前海开源基金投资部总监、基金经理崔宸龙在做客中国证券 报"中证点金汇"直播间谈及自身投资框架时表示,产业趋势是其较为看重的一个要素,好公司往往也是 处于产业发展、技术革新的大行业方向上。投资价值的锚定主要还是使用现金流折现(DCF)模型进行评 估。 ...
海通国际:维持百济神州(06160)“优于大市”评级 目标价213.10港元
智通财经网· 2025-11-12 01:21
Core Viewpoint - Haitong International has raised its revenue forecasts for BeiGene (06160) for FY25-27, expecting revenues of $5.3 billion, $6.4 billion, and $7.1 billion respectively, reflecting a CAGR of 23% over three years, due to better-than-expected sales and R&D expenses [1] Group 1: Financial Performance - In Q3 2025, BeiGene achieved revenues of $1.41 billion, a year-on-year increase of 41% and a quarter-on-quarter increase of 7.7%, with product revenues of $1.4 billion [2] - The company reported a gross margin of 86.1%, up 3.1 percentage points year-on-year [2] - R&D expenses were $520 million, up 5.5% year-on-year, while sales expenses were $530 million, up 16.2% year-on-year, resulting in an operating profit of $160 million [2] - The net profit for the quarter was $120 million, and management raised the full-year revenue guidance for 2025 to $5.1-5.3 billion [2] Group 2: Product Performance - The global revenue for Zebrutinib is expected to approach $3.9 billion in 2025, with Q3 revenues of $1.04 billion, a year-on-year increase of 50.8% and a quarter-on-quarter increase of 9.6% [3] - In the U.S., Zebrutinib generated $740 million, a year-on-year increase of 46.7%, while in Europe, it reached $160 million, a year-on-year increase of 67.7% [3] - The global revenue for Tislelizumab (PD-1) was $190 million, reflecting a year-on-year increase of 16.7% [3] Group 3: Clinical Development - In the hematological malignancies area, the company is focusing on the BCL-2 inhibitor and BTK CDAC, with plans to submit a U.S. market application for Zebrutinib in R/R MCL [4] - The management plans to initiate a Phase III clinical trial for multiple myeloma in 2026, using a regimen based on the BCL-2 inhibitor [4] - For the solid tumor area, the company is advancing the CDK4 inhibitor and B7-H4 ADC, with plans to start a Phase III trial for HR+/HER2- breast cancer in 1H26 [5]