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Biogen's Q2 Earnings & Sales Beat, 2025 Outlook Raised, Stock Up
ZACKS· 2025-07-31 23:50
Key Takeaways BIIB's Q2 EPS of $5.47 and revenues of $2.65B beat estimates, driven by new drugs.Vumerity, Leqembi, and Zurzuvae showed strong demand and sequential sales growth in the quarter.BIIB raised its 2025 EPS outlook to $15.50-$16.00 and now sees flat full-year revenue versus prior decline.Biogen (BIIB) reported second-quarter 2025 adjusted earnings per share (EPS) of $5.47, which significantly beat the Zacks Consensus Estimate of $3.93. Earnings rose 4% year over year on a reported basis.Total reve ...
Biogen(BIIB) - 2025 Q2 - Earnings Call Transcript
2025-07-31 21:32
Biogen (BIIB) Q2 2025 Earnings Call July 31, 2025 08:30 AM ET Company ParticipantsTim Power - Head of IRChristopher Viehbacher - President, CEO & DirectorPriya Singhal - EVP & Head - DevelopmentAlisha Alaimo - President & Head - North AmericaRobin Kramer - EVP & CFOPhilip Nadeau - MD, Health Care – BiotechnologyMichael Yee - Managing DirectorUmer Raffat - Senior Managing DirectorBrian Abrahams - MD & Co-Head of Biotechnology ResearchSalveen Richter - Biotechnology Equity ResearchConference Call Participants ...
Biogen(BIIB) - 2025 Q2 - Earnings Call Transcript
2025-07-31 21:30
Biogen (BIIB) Q2 2025 Earnings Call July 31, 2025 08:30 AM ET Speaker0Good morning. My name is Cynthia, and I will be your conference operator today. At this time, I would like to welcome everyone to the Biogen Second Quarter twenty twenty five Earnings Call and Business Update. All lines have been placed on mute to prevent any background noise. After the speakers' remarks, there will be a question and answer question remarks, Today's conference is being recorded. AndThank you. I would now like to turn the ...
Biogen(BIIB) - 2025 Q2 - Earnings Call Presentation
2025-07-31 20:30
July 31, 2025 SECOND QUARTER 2025 FINANCIAL RESULTS AND BUSINESS UPDATE FORWARD-LOOKING STATEMENTS This presentation and the discussions during this conference call contains forward-looking statements, relating to: our strategy and plans; potential of, and expectations for, our commercial business and pipeline programs; capital allocation and investment strategy; clinical development programs, clinical trials, and data readouts and presentations; regulatory discussions, submissions, filings, and approvals; ...
Biogen(BIIB) - 2025 Q2 - Quarterly Report
2025-07-31 18:05
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 Form 10-Q ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended June 30, 2025 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Commission File Number 0-19311 BIOGEN INC. (Exact name of registrant as specified in its charter) (State or other jurisdiction of incorporation or organization) Delaware 33-0112644 (I.R.S. Employer Ide ...
Biogen (BIIB) Q2 Earnings on the Horizon: Analysts' Insights on Key Performance Measures
ZACKS· 2025-07-30 22:15
Wall Street analysts forecast that Biogen Inc. (BIIB) will report quarterly earnings of $3.94 per share in its upcoming release, pointing to a year-over-year decline of 25.4%. It is anticipated that revenues will amount to $2.32 billion, exhibiting a decrease of 5.8% compared to the year-ago quarter.Over the last 30 days, there has been a downward revision of 2.7% in the consensus EPS estimate for the quarter, leading to its current level. This signifies the covering analysts' collective reconsideration of ...
全球制药业洞察 | 断崖式削减!阿尔兹海默药物发展受阻
彭博Bloomberg· 2025-07-30 14:04
阿尔茨海默药物市场前景 - 渤健-卫材的Leqembi和礼来的Kisunla预计将主导阿尔茨海默药物市场 但2030年市场规模预期从130亿美元大幅下调至60亿美元 [3] - 研发挫折、安全性风险及药物应用缓慢是市场预期下调的主要原因 风险调整后销售预期削减70亿美元 [3][8] - 到2030年 阿尔茨海默药物总销售预计达60亿美元 其中近10亿美元来自新机制药物 [5][16] 主要药物销售预测 - 2025年Leqembi与Kisunla合计销售或达5.91亿美元 2030年有望增长近七倍至40亿美元 较市场普遍预期低24% [4] - Leqembi的2025年销售预期为4.01亿美元 较市场普遍预期低16% 2030年渤健销售分成预计为9.48亿美元 [13] - Kisunla的2025年销售预测为1.79亿美元 较市场普遍预期高出42% 主要得益于剂量调整安全性提升 [4] 市场竞争格局 - 渤健-卫材预计在2028年前主导市场 但礼来有望在2029年凭借Kisunla及后续药物remternetug实现反超 [15] - 诺和诺德的semaglutide和罗氏的troninemab等新机制药物可能分割市场 压缩第一代抗体的市场份额 [11][15] - 欧盟批准将APOE-ε4纯合子患者排除在外 限制了Leqembi的短期应用范围 [4] 行业挑战与调整 - 自2024年6月以来 后期临床试验失败导致销售预测下调54% 2025-2030年风险调整后预期缩水70亿美元 [8] - 约半数医生质疑Leqembi疗效 70%符合条件患者拒绝用药 安全性担忧和获取障碍持续拖累应用 [11][13] - 渤健对Leqembi依赖度高 该药物2030年收入预计占公司总收入10% 而礼来的阿尔茨海默药物收入占比较小 [13][15]
Biogen Gears Up to Report Q2 Earnings: Here's What to Expect
ZACKS· 2025-07-28 23:26
Key Takeaways BIIB's Q2 results may reflect weaker MS drug sales but growth from newer products.Leqembi and Zurzuvae revenues are likely to have risen in the second quarter.Skyclarys faced mixed dynamics across U.S. and global marketsBiogen (BIIB) will report second-quarter 2025 results on July 31, before market open. In the last reported quarter, the company's earnings missed expectation by 7.4%. The Zacks Consensus Estimate for second-quarter sales and earnings is pegged at $2.32 billion and $3.95 per sha ...
小核酸药物:治疗潜力显现,蕴藏BD机遇
东方证券· 2025-07-27 17:44
报告行业投资评级 - 看好(维持) [6] 报告的核心观点 - 小核酸有望成小分子和抗体后的第三大类药物 具备靶标广、特异性强、研发效率高和给药间隔长等优势 [9] - 罕见病商业化成熟 慢性病长效优势显现 截至24年Spinraza累计全球销售额近138亿美元 Leqivo 25Q1全球销售额2.6亿美元 同比+72% [9] - 海外TTR领域重要转折到来 CVD三期数据读出在即 国内慢乙肝迎来新基石疗法 心血管领域竞争激烈 [9] - 对外大额BD频现 凸显早期慢病管线潜力 未来有望持续诞生重磅BD [9] - 建议关注国内布局慢乙肝、心血管领域小核酸药物管线相关优质标的 如恒瑞医药、中国生物制药等 [9] 根据相关目录分别进行总结 一、小核酸:有望成为小分子和抗体后的第三大类药物 - 靶向核酸机制独特 成药潜力超传统药物 靶点为细胞内mRNA 选择性高、脱靶毒性低且药物相互作用风险低 半衰期和药效持续时间长 给药频率可达每6个月1次 [23] - 以修饰和递送为壁垒 生产工艺决定成败 化学修饰与递送系统是核心技术壁垒 ASO主要依赖化学修饰 siRNA主要依赖递送系统 GalNAc已成突破性技术平台 [41][48] - 罕见病商业化渐成熟 慢性病长效优势显现 ASO以罕见病为主 Spinraza商业化最成功 siRNA是慢病创新长效疗法 Leqivo销售持续放量 [60][77][82] 二、海外数个里程碑将至,国内常见慢病多点开花 - 海外:TTR重要转折到来 CVD三期数据读出在即 Vutrisiran突破ATTR - CM 百亿美元市场有望三足鼎立 Pelacarsen等有望在25年读出3期临床数据 [95][96][102] - 国内:慢乙肝迎来新基石疗法 心血管竞争激烈 慢乙肝领域GSK836或明年上市 国内公司管线紧随其后 心血管领域APOC3等靶点扎堆 剑指降脂和降压赛道 其他领域NASH实现对外授权 痛风领域前景广阔 [111][119][124] 三、投资建议与投资标的 - 小核酸药物优势明显 有望成新技术路径 建议关注国内布局慢乙肝、心血管领域小核酸药物管线相关优质标的 如恒瑞医药、中国生物制药等 [9][126]
ZURZUVAE® (zuranolone) Receives Positive Opinion from CHMP for the Treatment of Women with Postpartum Depression
Globenewswire· 2025-07-25 19:20
文章核心观点 - 欧洲药品管理局人用药品委员会(CHMP)对渤健公司(Biogen)的ZURZUVAE给出积极意见,建议批准其用于治疗产后抑郁症(PPD),若获欧盟委员会(EC)批准,ZURZUVAE将成欧盟首个专门治疗PPD女性抑郁症状的疗法 [1] ZURZUVAE药物相关 - ZURZUVAE是每日一次、口服、为期14天的药物,2023年获美国食品药品监督管理局(FDA)批准,是一种神经活性类固醇(NAS)GABA - A受体正向别构调节剂(PAM) [1][6] - ZURZUVAE由Sage Therapeutics发现,2020年渤健与Sage Therapeutics达成合作,联合在美国开发和商业化该药物,渤健获美国以外(除日本、台湾和韩国)独家开发和商业化权利 [7] 产后抑郁症(PPD)情况 - PPD是与怀孕相关的常见病症,症状包括情绪低落、焦虑等,若不治疗,症状可能持续并影响母婴健康,欧洲约5 - 20%怀孕女性有PPD症状,且因各国筛查和管理指南不同,许多病例可能未被诊断和治疗,围产期自杀是欧洲孕产妇死亡主要原因 [2][3] CHMP推荐依据 - CHMP对ZURZUVAE的推荐基于SKYLARK研究,该研究达到主要终点,第15天汉密尔顿抑郁量表17项总分(HAMD - 17)较基线显著降低,所有关键次要终点也达成,第3天起抑郁症状显著减轻并持续到第45天,ZURZUVAE总体耐受性良好,最常见副作用为嗜睡、头晕和镇静 [4] 审批进展 - CHMP对ZURZUVAE的推荐将由EC审查,预计2025年第三季度作出最终决定,美国FDA于2023年8月批准ZURZUVAE,美国缉毒局(DEA)于2023年10月31日将其列为IV类管制物质 [5] 关于渤健公司 - 渤健成立于1978年,是领先的生物技术公司,致力于创新科学,为患者提供新药,通过深入理解人类生物学和利用不同疗法,推进一流治疗方法,以实现长期增长 [8]