BIOGEN INC

NASDAQ: BIIB (Biogen Inc.)

最近更新时间: 05 Aug, 5:43PM

132.89

0.69 (0.52%)

前收盘价格 132.20
收盘价格 131.65
成交量 1,323,863
平均成交量 (3个月) 1,498,248
市值 19,483,668,480
市盈率 (P/E TTM) 12.73
预期市盈率 (P/E Forward) 9.23
价格/销量 (P/S) 1.93
股市价格/股市净资产 (P/B) 1.10
52周波幅
110.04 (-17%) — 207.59 (56%)
利润日期 29 Oct 2025
营业毛利率 15.07%
营业利益率 (TTM) 28.05%
稀释每股收益 (EPS TTM) 10.12
季度收入增长率 (YOY) 6.10%
季度盈利增长率 (YOY) -38.90%
总债务/股东权益 (D/E MRQ) 39.00%
流动比率 (MRQ) 1.44
营业现金流 (OCF TTM) 2.58 B
杠杆自由现金流 (LFCF TTM) 3.43 B
资产报酬率 (ROA TTM) 5.43%
股东权益报酬率 (ROE TTM) 9.19%

市场趋势

短期 中期
行业 Drug Manufacturers - General (US) 混合的 混合的
Drug Manufacturers - General (全球的) 混合的 混合的
股票 Biogen Inc. 看跌 看跌

AIStockmoo 评分

-0.5
分析师共识 -0.5
内部交易活动 NA
价格波动 -2.0
技术平均移动指标 0.0
技术振荡指标 0.5
平均 -0.50

相关股票

股票 市值 DY P/E(TTM) P/B
BIIB 19 B - 12.73 1.10
AZN 226 B 1.44% 29.27 5.54
SNY 118 B 4.58% 16.37 1.48
AMGN 159 B 3.18% 24.16 20.57
GILD 141 B 2.08% 23.78 7.12
GRFS 6 B 1.73% 28.00 1.09

Biogen and Idec merged in 2003, combining forces to market Biogen's multiple sclerosis drug Avonex and Idec's cancer drug Rituxan. Today, Rituxan and next-generation antibody Gazyva (oncology) and Ocrevus (multiple sclerosis) are marketed via a collaboration with Roche. Biogen markets several multiple sclerosis drugs including Plegridy, Tysabri, Tecfidera, and Vumerity. Biogen's newer products include Spinraza (SMA, with partner Ionis), Leqembi (Alzheimers, with partner Eisai), Skyclarys (Friedreich's Ataxia, Reata), Zurzuvae (postpartum depression, Sage), and Qalsody (ALS, Ionis). Biogen has several drug candidates in phase 3 trials in neurology, immunology, and rare diseases.

部门 Healthcare
行业 Drug Manufacturers - General
投资方式 Mid Value
内部持股比例 0.19%
机构持股比例 92.79%
52周波幅
110.04 (-17%) — 207.59 (56%)
目标价格波幅
118.00 (-11%) — 219.00 (64%)
219.00 (RBC Capital, 64.80%) 购买
139.50 (4.97%)
118.00 (Piper Sandler, -11.21%) 保留
平均值 155.17 (16.77%)
总计 2 购买, 4 保留
平均价格@调整类型 132.51
公司 日期 目标价格 调整类型 价格@调整类型
Piper Sandler 14 Aug 2025 118.00 (-11.20%) 保留 134.94
12 Jun 2025 115.00 (-13.46%) 保留 132.31
Citigroup 01 Aug 2025 135.00 (1.59%) 保留 131.95
HC Wainwright & Co. 01 Aug 2025 194.00 (45.99%) 购买 131.95
26 Jun 2025 187.00 (40.72%) 购买 126.92
Morgan Stanley 01 Aug 2025 144.00 (8.36%) 保留 131.95
RBC Capital 01 Aug 2025 219.00 (64.80%) 购买 131.95
27 Jun 2025 213.00 (60.28%) 购买 126.08
Wedbush 12 Jun 2025 121.00 (-8.95%) 保留 132.31

该时间范围内无数据。

日期 类型 细节
02 Sep 2025 公告 Biogen and Stoke Therapeutics Present Data at the 36th International Epilepsy Congress that Support the Potential for Zorevunersen to be the First Disease-Modifying Medicine for Dravet Syndrome
02 Sep 2025 公告 Eisai Initiated Rolling Supplemental Biologics License Application to the U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease Under Fast Track Status
02 Sep 2025 公告 Eisai Initiated Rolling Supplemental Biologics License Application to the U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease Under Fast Track Status
02 Sep 2025 公告 Stoke Therapeutics and Biogen Present Data at the 36th International Epilepsy Congress that Support the Potential for Zorevunersen to be the First Disease-Modifying Medicine for Dravet Syndrome
02 Sep 2025 公告 Eisai Initiated Rolling Supplemental Biologics License Application to the U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status
02 Sep 2025 公告 Biogen and Stoke Therapeutics Present Data at the 36th International Epilepsy Congress that Support the Potential for Zorevunersen to be the First Disease-Modifying Medicine for Dravet Syndrome
29 Aug 2025 公告 FDA Approves LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection for Maintenance Dosing for the Treatment of Early Alzheimer's Disease
29 Aug 2025 公告 FDA Approves LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection for Maintenance Dosing for the Treatment of Early Alzheimer's Disease
29 Aug 2025 公告 FDA Approves LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection for Maintenance Dosing for the Treatment of Early Alzheimer's Disease
25 Aug 2025 公告 Stoke Therapeutics and Biogen Announce Presentations of Clinical Data from Studies of Zorevunersen for the Potential Treatment of Dravet Syndrome at the 36th International Epilepsy Congress
25 Aug 2025 公告 Biogen and Stoke Therapeutics Announce Presentations of Clinical Data from Studies of Zorevunersen for the Potential Treatment of Dravet Syndrome at the 36th International Epilepsy Congress
25 Aug 2025 公告 Biogen and Stoke Therapeutics Announce Presentations of Clinical Data from Studies of Zorevunersen for the Potential Treatment of Dravet Syndrome at the 36th International Epilepsy Congress
25 Aug 2025 公告 Austria and Germany to become the first markets in the European Union (EU) to launch LEQEMBI® (lecanemab)
25 Aug 2025 公告 Austria and Germany to become the first markets in the European Union (EU) to launch LEQEMBI® (lecanemab)
11 Aug 2025 公告 Stoke Therapeutics and Biogen Announce First Patient Dosed in Phase 3 EMPEROR Study of Zorevunersen, a Potential Disease-Modifying Treatment for Dravet Syndrome
11 Aug 2025 公告 Biogen and Stoke Therapeutics Announce First Patient Dosed in Phase 3 EMPEROR Study of Zorevunersen, a Potential Disease-Modifying Treatment for Dravet Syndrome
30 Jul 2025 公告 Two-Year Real-World Study of LEQEMBI® in the United States Presented at Alzheimer's Association International Conference (AAIC) 2025
30 Jul 2025 公告 New Data Presented at AAIC Demonstrates Investigational LEQEMBI® (lecanemab-irmb) 360 mg Subcutaneous Maintenance Dosing Could Offer a New Option for Ongoing Treatment of Early Alzheimer's Disease
30 Jul 2025 公告 Two-Year Real-World Study of LEQEMBI® in the United States Presented at Alzheimer's Association International Conference (AAIC) 2025
30 Jul 2025 公告 Early Alzheimer's Patients Continue to Benefit from Four Years of LEQEMBI® (lecanemab-irmb) Therapy New Clinical Data Presented at AAIC
25 Jul 2025 公告 ZURZUVAE® (zuranolone) Receives Positive Opinion from CHMP for the Treatment of Women with Postpartum Depression
25 Jul 2025 公告 ZURZUVAE® (zuranolone) Receives Positive Opinion from CHMP for the Treatment of Women with Postpartum Depression
21 Jul 2025 公告 Biogen to Highlight Scientific Progress Across Alzheimer’s Disease at the Alzheimer’s Association International Conference 2025
21 Jul 2025 CNBC FDA taps biotech industry veteran as RFK Jr.'s top drug regulator 
21 Jul 2025 公告 Biogen to Highlight Scientific Progress Across Alzheimer’s Disease at the Alzheimer’s Association International Conference 2025
21 Jul 2025 公告 Biogen Announces $2 Billion Manufacturing Investment in North Carolina’s Research Triangle Park in Conjunction with its 30th Anniversary
10 Jul 2025 公告 Biogen and Stoke Therapeutics Announce Presentation of Data from Studies of Zorevunersen, an Investigational Medicine for Dravet syndrome, at the 16th European Paediatric Neurology Society (EPNS) Congress
10 Jul 2025 公告 Biogen and Stoke Therapeutics Announce Presentation of Data from Studies of Zorevunersen, an Investigational Medicine for Dravet syndrome, at the 16th European Paediatric Neurology Society (EPNS) Congress
10 Jul 2025 公告 Stoke Therapeutics and Biogen Announce Presentation of Data from Studies of Zorevunersen, an Investigational Medicine for Dravet syndrome, at the 16th European Paediatric Neurology Society (EPNS) Congress
30 Jun 2025 公告 Biogen Initiates Phase 3 Study of Felzartamab for the Treatment of Primary Membranous Nephropathy
30 Jun 2025 公告 Biogen Initiates Phase 3 Study of Felzartamab for the Treatment of Primary Membranous Nephropathy
27 Jun 2025 公告 New Data for Nusinersen Underscore Biogen’s Commitment to Advancing Clinical Research to Improve Outcomes in SMA
27 Jun 2025 公告 New Data for Nusinersen Underscore Biogen’s Commitment to Advancing Clinical Research to Improve Outcomes in SMA
25 Jun 2025 公告 Biogen to Advance Investigational Spinal Muscular Atrophy Asset to Registrational Studies Based on Positive Interim Phase 1 Results
25 Jun 2025 公告 Biogen to Advance Investigational Spinal Muscular Atrophy Asset to Registrational Studies Based on Positive Interim Phase 1 Results
18 Jun 2025 公告 Biogen Initiates Phase 3 Pediatric Study of Omaveloxolone for the Treatment of Friedreich Ataxia
18 Jun 2025 公告 Biogen Initiates Phase 3 Pediatric Study of Omaveloxolone for the Treatment of Friedreich Ataxia
12 Jun 2025 公告 Dapirolizumab Pegol Phase 3 Data in SLE Presented at the Annual European Congress of Rheumatology (EULAR) Show Improvement in Fatigue and Reduction in Disease Activity
12 Jun 2025 公告 Dapirolizumab Pegol Phase 3 Data in SLE Presented at the Annual European Congress of Rheumatology (EULAR) Show Improvement in Fatigue and Reduction in Disease Activity
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