BIOGEN INC

NASDAQ: BIIB (Biogen Inc.)

Kemas kini terakhir: 29 Nov, 8:16AM

182.09

0.15 (0.08%)

Penutupan Terdahulu 181.94
Buka 182.00
Jumlah Dagangan 465,267
Purata Dagangan (3B) 1,812,966
Modal Pasaran 26,713,016,320
Harga / Pendapatan (P/E TTM) 16.61
Harga / Pendapatan (P/E Ke hadapan) 11.31
Harga / Jualan (P/S) 2.57
Harga / Buku (P/B) 1.42
Julat 52 Minggu
110.04 (-39%) — 185.17 (1%)
Tarikh Pendapatan 30 Oct 2025
Margin Keuntungan 15.07%
Margin Operasi (TTM) 28.05%
EPS Cair (TTM) 10.12
Pertumbuhan Hasil Suku Tahunan (YOY) 6.10%
Pertumbuhan Pendapatan Suku Tahunan (YOY) -38.90%
Jumlah Hutang/Ekuiti (D/E MRQ) 39.00%
Nisbah Semasa (MRQ) 1.44
Aliran Tunai Operasi (OCF TTM) 2.58 B
Aliran Tunai Bebas Leveraj (LFCF TTM) 3.43 B
Pulangan Atas Aset (ROA TTM) 5.43%
Pulangan Atas Ekuiti (ROE TTM) 9.19%

Arah Aliran Pasaran

Jangka Pendek Jangka Sederhana
Industri Drug Manufacturers - General (US) Menaik Menurun
Drug Manufacturers - General (Global) Menaik Menurun
Stok Biogen Inc. Menurun Menurun

AISkor Stockmoo

-1.8
Konsensus Penganalisis -3.5
Aktiviti Orang Dalam NA
Volatiliti Harga -5.0
Purata Bergerak Teknikal -2.5
Osilator Teknikal 4.0
Purata -1.75

Saham Serupa

Stok Modal Pasaran DY P/E (TTM) P/B
BIIB 27 B - 16.61 1.42
AZN 282 B 1.72% 30.18 6.09
SNY 121 B 4.47% 16.24 1.41
AMGN 182 B 2.82% 26.13 19.34
GILD 154 B 2.55% 19.24 7.32
GRFS 7 B 1.96% 14.05 1.00

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.

Sektor Healthcare
Industri Drug Manufacturers - General
Gaya Pelaburan Mid Value
% Dimiliki oleh Orang Dalam 0.19%
% Dimiliki oleh Institusi 92.79%
Julat 52 Minggu
110.04 (-39%) — 185.17 (1%)
Julat Harga Sasaran
149.00 (-18%) — 210.00 (15%)
Tinggi 210.00 (RBC Capital, 15.33%) Beli
Median 173.50 (-4.72%)
Rendah 149.00 (Morgan Stanley, -18.17%) Pegang
Purata 177.50 (-2.52%)
Jumlah 3 Beli, 3 Pegang
Harga Purata @ Panggilan 153.33
Syarikat Tarikh Harga Sasaran Panggilan Harga @ Panggilan
Piper Sandler 21 Nov 2025 157.00 (-13.78%) Pegang 175.30
Stifel 06 Nov 2025 202.00 (10.93%) Beli 156.74
Bernstein 03 Nov 2025 157.00 (-13.78%) Pegang 151.44
RBC Capital 31 Oct 2025 210.00 (15.33%) Beli 154.27
Morgan Stanley 10 Oct 2025 149.00 (-18.17%) Pegang 146.57
Jefferies 25 Sep 2025 190.00 (4.34%) Beli 135.67

Tiada data dalam julat masa ini.

Tarikh Jenis Butiran
05 Dec 2025 Pengumuman Biogen and Stoke Therapeutics Present Data that Further Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 2025 American Epilepsy Society (AES) Annual Meeting
05 Dec 2025 Pengumuman Stoke Therapeutics and Biogen Present Data that Further Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 2025 American Epilepsy Society (AES) Annual Meeting
05 Dec 2025 Pengumuman Biogen and Stoke Therapeutics Present Data that Further Support the Disease-Modifying Potential of Zorevunersen, an Investigational Medicine for the Treatment of Dravet Syndrome, at the 2025 American Epilepsy Society (AES) Annual Meeting
03 Dec 2025 Pengumuman Eisai Presents New Data on the Continued and Expanding Benefit of LEQEMBI® (lecanemab-irmb) Maintenance Treatment in Early Alzheimer's Disease at the Clinical Trials on Alzheimer's Disease (CTAD) Conference 2025
02 Dec 2025 Pengumuman New Data Presented at the Clinical Trials on Alzheimer's Disease (CTAD) Conference 2025 Confirms Pharmacological Effect of LEQEMBI® (lecanemab-irmb) on Neurotoxic Aβ Protofibrils in CSF
01 Dec 2025 Pengumuman Stoke Therapeutics and Biogen Announce Presentations at the 2025 American Epilepsy Society Annual Meeting
25 Nov 2025 Pengumuman Eisai Completes Rolling Submission to U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status
24 Nov 2025 Pengumuman Biogen and Dayra Therapeutics Announce Research Collaboration to Discover and Develop Oral Macrocyclic Peptides for a Range of Immunological Conditions
24 Nov 2025 Pengumuman Biogen and Dayra Therapeutics Announce Research Collaboration to Discover and Develop Oral Macrocyclic Peptides for a Range of Immunological Conditions
20 Nov 2025 Pengumuman Biogen to Highlight New Lecanemab Data and Scientific Advances at the 18th Clinical Trials on Alzheimer’s Disease Conference
17 Nov 2025 Pengumuman High Dose Regimen of Nusinersen Receives Positive CHMP Opinion for the Treatment of Spinal Muscular Atrophy
17 Nov 2025 Pengumuman High Dose Regimen of Nusinersen Receives Positive CHMP Opinion for the Treatment of Spinal Muscular Atrophy
17 Nov 2025 Pengumuman Stoke Therapeutics and Biogen Announce Publication of Two-Year Natural History Data Demonstrating the Severity of Dravet Syndrome, Including Frequent Seizures and Significant Cognitive and Behavioral Impairments
17 Nov 2025 Pengumuman Biogen and Stoke Therapeutics Announce Publication of Two-Year Natural History Data Demonstrating the Severity of Dravet Syndrome, Including Frequent Seizures and Significant Cognitive and Behavioral Impairments
17 Nov 2025 Pengumuman Biogen and Stoke Therapeutics Announce Publication of Two-Year Natural History Data Demonstrating the Severity of Dravet Syndrome, Including Frequent Seizures and Significant Cognitive and Behavioral Impairments
14 Nov 2025 Pengumuman Biogen Completes Acquisition of Alcyone Therapeutics
14 Nov 2025 Pengumuman Biogen Completes Acquisition of Alcyone Therapeutics
03 Nov 2025 Pengumuman Biogen to Highlight Scientific Progress in Rare Kidney Disease at American Society of Nephrology (ASN) Kidney Week 2025
03 Nov 2025 Pengumuman Biogen to Highlight Scientific Progress in Rare Kidney Disease at American Society of Nephrology (ASN) Kidney Week 2025
24 Oct 2025 Pengumuman Biogen Licenses Oral C5aR1 Antagonist from Vanqua Bio to Expand Immunology Portfolio
24 Oct 2025 Pengumuman Biogen Licenses Oral C5aR1 Antagonist from Vanqua Bio to Expand Immunology Portfolio
22 Oct 2025 Pengumuman Biogen to Present Additional Results from Phase 3 Study of Dapirolizumab Pegol in Systemic Lupus Erythematosus at ACR Convergence 2025
22 Oct 2025 Pengumuman Biogen to Present Additional Results from Phase 3 Study of Dapirolizumab Pegol in Systemic Lupus Erythematosus at ACR Convergence 2025
13 Oct 2025 Pengumuman LEQEMBI® IQLIK™(lecanemab-irmb) Subcutaneous Autoinjector Named to TIME's "Best Inventions of 2025"
13 Oct 2025 Pengumuman LEQEMBI® IQLIK™(lecanemab-irmb) Subcutaneous Autoinjector Named to TIME’s “Best Inventions of 2025”
13 Oct 2025 Pengumuman LEQEMBI® IQLIK™(lecanemab-irmb) Subcutaneous Autoinjector Named to TIME’s “Best Inventions of 2025”
09 Oct 2025 Pengumuman Biogen and Stoke Therapeutics Present New Data at the 54th Child Neurology Society (CNS) Annual Meeting that Support the Potential of Zorevunersen as a Disease-Modifying Medicine for Dravet Syndrome
09 Oct 2025 Pengumuman Biogen and Stoke Therapeutics Present New Data at the 54th Child Neurology Society (CNS) Annual Meeting that Support the Potential of Zorevunersen as a Disease-Modifying Medicine for Dravet Syndrome
09 Oct 2025 Pengumuman Stoke Therapeutics and Biogen Present New Data at the 54th Child Neurology Society (CNS) Annual Meeting that Support the Potential of Zorevunersen as a Disease-Modifying Medicine for Dravet Syndrome
06 Oct 2025 Pengumuman Eisai and Biogen Announce U.S. Availability of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection Maintenance Dose for Treatment of Early Alzheimer's Disease
06 Oct 2025 Pengumuman Eisai and Biogen Announce U.S. Availability of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection Maintenance Dose for Treatment of Early Alzheimer’s Disease
06 Oct 2025 Pengumuman Eisai and Biogen Announce U.S. Availability of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection Maintenance Dose for Treatment of Early Alzheimer’s Disease
28 Sep 2025 Pengumuman “LEQEMBI®” (lecanemab) IV Maintenance Dosing for the Treatment of Early Alzheimer’s Disease Approved in China
28 Sep 2025 Pengumuman “LEQEMBI®” (lecanemab) IV Maintenance Dosing for the Treatment of Early Alzheimer’s Disease Approved in China
24 Sep 2025 Pengumuman LEQEMBI® (Lecanemab) Approved for the Treatment of Alzheimer’s Disease in Australia
24 Sep 2025 Pengumuman LEQEMBI® (Lecanemab) Approved for the Treatment of Alzheimer’s Disease in Australia
23 Sep 2025 Pengumuman Biogen Provides Regulatory Update on High Dose Regimen of Nusinersen
23 Sep 2025 Pengumuman Biogen Provides Regulatory Update on High Dose Regimen of Nusinersen
18 Sep 2025 Pengumuman Biogen to Acquire Alcyone Therapeutics, Expanding Drug Delivery Solution Portfolio for Key Product and Pipeline Candidates
18 Sep 2025 Pengumuman Biogen to Acquire Alcyone Therapeutics, Expanding Drug Delivery Solution Portfolio for Key Product and Pipeline Candidates
17 Sep 2025 Pengumuman Biogen Receives European Commission Approval for ZURZUVAE® (zuranolone), the First and Only Treatment Approved for Women with Postpartum Depression in Europe
17 Sep 2025 Pengumuman Biogen Receives European Commission Approval for ZURZUVAE® (zuranolone), the First and Only Treatment Approved for Women with Postpartum Depression in Europe
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