Pakin Jarerndee/iStock via Getty Images PORTFOLIO OBSERVATIONS The following positions were our largest additions to the portfolio during the quarter: Blueprint Medicines Corporation (5.3% of net assets as of June 30, 2025), is a pharmaceutical company focused on medicines for genomically defined cancers ...

Core Insights - The Ademi Firm is investigating Blueprint (Nasdaq: BPMC) regarding its transaction with Sanofi, focusing on potential insider benefits and conflicts of interest [1] Group 1 - Blueprint insiders received substantial benefits as part of change of control arrangements [1] - Certain insiders may have had conflicts of interest related to the transaction [1]

Core Viewpoint - Sanofi has successfully completed the acquisition of Blueprint Medicines, enhancing its portfolio with a commercialized medicine and a promising pipeline focused on systemic mastocytosis and other KIT-driven diseases [1][6]. Group 1: Acquisition Details - The acquisition includes Ayvakit/Ayvakyt (avapritinib), the only approved medicine for advanced and indolent systemic mastocytosis in the US and EU [3][10]. - Sanofi also acquired elenestinib, a next-generation investigational medicine for systemic mastocytosis, currently undergoing a phase 2/3 clinical study [4]. - Additionally, BLU-808, an investigational oral KIT inhibitor, was part of the acquisition, targeting a range of inflammatory diseases [5]. Group 2: Financial Aspects - The tender offer for Blueprint's shares was completed on July 17, 2025, with all conditions satisfied [6]. - Sanofi financed the acquisition through cash on hand and proceeds from commercial paper issuances, indicating it will not significantly impact the company's financial guidance for 2025 [7]. - The acquisition is expected to be immediately accretive to gross margin and business operating income, as well as EPS after 2026 [7]. Group 3: Market Impact - Following the acquisition, Blueprint common stock will cease trading on the NASDAQ Global Select Stock Market as of July 18, 2025 [9]. - All shares not validly tendered will convert to a cash payment of $129.00 per share, plus potential contingent payments of up to $6.00 per share based on milestone achievements [8].

Core Viewpoint - Monteverde & Associates PC is investigating Blueprint Medicines Corporation regarding its proposed sale to Sanofi, which involves a cash payment of $129.00 per share and contingent value rights for future milestone payments [1]. Group 1: Transaction Details - Sanofi will pay $129.00 per share in cash at closing for Blueprint Medicines Corporation [1]. - Shareholders will receive one non-tradeable contingent value right (CVR) for potential milestone payments of $2.00 and $4.00, contingent on future development and regulatory milestones for BLU-808 [1]. Group 2: Legal Firm Background - Monteverde & Associates PC is recognized as a Top 50 Firm in the 2024 ISS Securities Class Action Services Report and has recovered millions for shareholders [1]. - The firm is located in the Empire State Building in New York City and specializes in class action securities litigation [2].

Core Insights - Blueprint Medicines Corporation has showcased its leadership in advancing care for patients with systemic mastocytosis (SM) through data presentations at major congresses, emphasizing the effectiveness of AYVAKIT®/AYVAKYT® (avapritinib) as a standard treatment for both indolent and advanced forms of SM [1][2][9]. Data Presentation Highlights - The presentations included large patient populations from the PIONEER, PATHFINDER, and EXPLORER trials, demonstrating long-term benefits of AYVAKIT with follow-up periods of up to five years for indolent systemic mastocytosis (ISM) and 6.5 years for advanced SM [2][5]. - AYVAKIT has shown transformative clinical outcomes, including sustained disease control in ISM and prolonged survival in advanced SM, leading to an expanded view among clinicians regarding appropriate candidates for disease-modifying therapy [2][7]. Clinical Efficacy and Safety - AYVAKIT demonstrated robust improvements in overall symptoms and quality of life measures over 144 weeks, with a low treatment-related adverse event discontinuation rate of 3% and common adverse events including low-grade edemas, headache, and nausea [7][23]. - The Revised Mutation-Adjusted Risk Score (MARS-R) tool was validated for assessing overall survival risks in advanced SM patients treated with AYVAKIT, showing meaningful survival benefits across all prognostic categories [7][12]. Disease Burden and Patient Impact - The PRISM study highlighted the substantial disease burden faced by patients with ISM, including physical, social, and emotional challenges that significantly disrupt daily life [6][12]. - Patients reported various disease-related impacts, such as limitations in physical activities and work, as well as issues with pain, anxiety, and adjustments in daily routines to avoid triggers [8][12]. Regulatory and Market Position - AYVAKIT is the first and only FDA-approved treatment targeting the root cause of SM, with approvals for both advanced SM and ISM, and is marketed in 16 countries globally [14][26]. - The company aims to expand its impact by advancing a broad pipeline of programs in mast cell diseases and solid tumors, leveraging its established research and commercial capabilities [26].

Group 1 - Sanofi announced a plan to acquire Blueprint Medicines for $9.1 billion, aiming to integrate Blueprint's rare disease and immunology pipeline assets to fill the profit gap after the patent expiration of Dupixent in 2031/32 [1][2] - The acquisition will be conducted at a cash price of $129 per share, representing a 27% premium over the closing price on May 30, with potential additional payments based on the success of Blueprint's drug BLU-808 [1][2] - Goldman Sachs maintains a "neutral" rating on Sanofi with a target price of €117 (ADR $67) following the announcement of the acquisition [1] Group 2 - Key assets in the acquisition include the approved tyrosine kinase inhibitor Ayvakit and the investigational drug BLU-808, which targets non-mutant KIT for chronic urticaria and allergic asthma [2] - Ayvakit is projected to reach peak sales of €2.35 billion by 2033 with a gross margin of 95%, while BLU-808 is expected to achieve peak sales of $2.7 billion (€1.7 billion) by 2033 [2] - The acquisition is expected to strengthen Sanofi's position in the rare disease sector and support its immunology pipeline, serving as a long-term alternative to Dupixent [2]

Group 1: Stock Movements and Market Reactions - JunDa Co., Ltd. (02865) fell by 12.69% due to weak fundamentals, expected shareholder sell-off, and cash flow concerns [1] - Rongchang Biopharmaceutical (09995) rose by 4.61% after ASCO announced positive data for RC108 combined with vorinostat, enhancing its commercialization prospects [1] - Datang Gold (08299) increased by 7.27% as it partnered with Wuxi to develop AI mining applications, benefiting from gold's safe-haven demand [1] - Kanglong Chemical (03759) gained 4.35% by investing in a biopharmaceutical fund, strengthening its investment ecosystem [1] - Automotive stocks surged following a significant increase in May's new energy vehicle sales, with Li Auto (2015) rising nearly 6% and Great Wall Motors (2333) up over 3% [1] - Gold stocks led the market as COMEX gold prices returned to $3,400, with Goldman Sachs predicting $4,200, driven by geopolitical tensions [1] Group 2: Company-Specific Developments - Changfei Optical Fiber (06869) rose by 8.34% as its Wuhan base began mass production of 6-inch silicon carbide wafers, achieving a 97% yield rate [2] - China Shipbuilding Defense (00317) increased by 7.58% after securing the highest global new orders from January to April, with Q1 net profit up 1,099% [2] - Hengrui Medicine (00013) rose by 5.09% as SACHI III phase data met expectations, opening up market space for MET amplification lung cancer treatment [2] - Lepu Medical Technology (02157) gained 5.76% following positive ASCO data for its ADC drug MRG003, boosting approval expectations for nasopharyngeal carcinoma [2] - Aidi Kang Holdings (09860) increased by 5.2% after acquiring Suzhou Yuande Youqin to enhance blood disease diagnostics [2] - NetDragon (00777) rose by 5.82% due to its collaboration with Thailand on an AI education platform, attracting investor interest [2] Group 3: Notable Market Trends - China Everbright Holdings (00165) surged over 21% following the enactment of Hong Kong's stablecoin regulations, with Circle's IPO expectations boosting related equity valuations [3] - iFlytek Medical (02506) rose by 6.62% as its medical AI model demonstrated superior accuracy, supported by favorable policies [3] - MicroPort NeuroTech (02172) increased by 9.59% as it initiated clinical research on brain-machine interfaces, benefiting from policy incentives [3] - Longpan Technology (02465) rose by 14.9% after its subsidiary signed a $7.1 billion contract with Yiwei Lithium Energy for lithium iron phosphate [4] - Hansoh Pharmaceutical (03692) gained 3.85% after reaching a global licensing agreement with Regeneron, receiving an $80 million upfront payment [4] Group 4: U.S. Market Highlights - Steel and aluminum stocks surged over 10%-28% as Trump proposed increasing steel tariffs to 50%, benefiting domestic companies [5] - Blueprint Medicines (BPMC.US) rose by 26% following Sanofi's $9.1 billion acquisition, enhancing its rare disease pipeline [5] - BioNTech (BNTX.US) increased by 18% due to a collaboration with Bristol-Myers Squibb, securing a $1.5 billion upfront payment [5] - Applied Digital (APLD.US) surged by 48.46% after signing a $7 billion AI data center lease, validating its business model [5] - Tempus AI (TEM.US) rose by 15% as it launched an AI medical innovation plan, attracting investor interest [7]

（原标题：潜在总金额95亿美元 赛诺菲收购罕见病疗法公司Blueprint） 经济观察网讯 据赛诺菲官网消息，当地时间6月2日，赛诺菲与总部位于美国的上市生物制药公司 Blueprint Medicines Corporation（Blueprint）达成协议，赛诺菲将收购专注于系统性肥大细胞增多症 （SM，一种罕见免疫疾病）及其他 KIT 驱动疾病的 Blueprint。 此次收购包括一款罕见免疫疾病药物 Ayvakit/Ayvakyt（avapritinib），已获美国和欧盟批准，以及一条 有前景的晚期和早期免疫学研发管线。此外，Blueprint 在过敏科、皮肤科和免疫学领域的既有影响力 预计将增强赛诺菲不断壮大的免疫学研发管线。 根据收购条款，赛诺菲将在交割时以每股129.00 美元现金支付，代表约91亿美元的股权价值。Blueprint 股东还将获得一份不可交易的或有价值权（CVR），该权利使持有人有权分别因 BLU-808 未来开发和 监管里程碑的达成而获得每份 CVR 2美元和4美元的两笔潜在里程碑付款。包括潜在CVR付款在内的交 易总股权价值，按完全稀释计算约为95亿美元。 Ayvakit 在 ...

Core Insights - Sanofi has entered into a definitive agreement to acquire Blueprint Medicines for a total deal value of up to $9.5 billion, with BPMC shares rising 26% following the announcement [1][6] - The acquisition is expected to be completed in the third quarter of 2025, subject to customary closing conditions [1] - The deal will enhance Sanofi's immunology portfolio by adding Blueprint Medicines' marketed product Ayvakit and its innovative pipeline candidates [2][5] Financial Details - Sanofi will pay $129 per share in cash, representing a 27% premium over BPMC's closing price, resulting in an equity value of approximately $9.1 billion [9] - Blueprint Medicines shareholders will also receive contingent value rights (CVRs) tied to future milestones for BLU-808, potentially increasing the total equity value to $9.5 billion [10] - Ayvakit generated $149.4 million in sales in Q1 2025, reflecting a 61% year-over-year increase, with projections of reaching $2 billion by 2030 [7][6] Strategic Intent - The acquisition aims to reduce Sanofi's reliance on Dupixent by expanding its immunology portfolio, which includes 12 potential blockbuster assets in phase III development [12][14] - Sanofi's first-quarter 2025 sales from Dupixent reached €3.48 billion, accounting for about a third of the company's total revenues, indicating the importance of diversifying its product offerings [14]

Core Viewpoint - Johnson Fistel, PLLP has initiated an investigation into potential breaches of fiduciary duties by the board members of Blueprint Medicines Corporation in relation to its proposed sale to Sanofi [1] Group 1: Acquisition Details - Blueprint Medicines has entered into a definitive agreement with Sanofi to sell all outstanding shares for $129.00 per share in cash, along with a non-tradeable contingent value right that could yield two milestone payments of $2 and $4 for future development and regulatory achievements related to BLU-808 [2] - The transaction agreement includes a provision that restricts Blueprint's ability to solicit or accept superior proposals, imposing a significant termination fee if the board pursues a competing bid [3] Group 2: Market Analysis - A Wall Street analyst has set a price target of $167 per share for Blueprint's common stock, which is significantly higher than the agreed transaction price of $129.00 [3]