다른 서비스와 비교했을 때 BMY 의 PS 비율은 어느 정도인가요?

BMY은 Price-To-Sales 비율(2.2x)을 기준으로 볼 때 동종 업계 평균(3.8x)과 비교했을 때 좋은 가치를 가지고 있습니다.

BMY 의 PS 비율은 European Pharmaceuticals 업계의 다른 회사와 어떻게 비교됩니까?

BMY 은 Price-To-Sales 2.2 Swiss Pharmaceuticals 업계 평균( 4.7 x).

BMY 의 PS 비율과 공정 PS 비율은 어떻게 되나요? 회사의 예상 수익 성장률, 이익 마진 및 기타 위험 요소를 고려한 예상 PS 비율입니다.

BMY 은 예상 2.2 Price-To-Sales Price-To-Sales ( 5.8 x).

미래 현금 흐름을 볼 때 BMY 의 공정 가격은 얼마인가요? 이 추정에는 할인된 현금흐름 모델을 사용합니다.

BMY ( CHF54.24 )는 당사 추정치인 [[공정 가치]]( CHF165.01 )

애널리스트의 12개월 전망은 무엇이며 컨센서스 목표가에 대한 통계적 신뢰도가 있나요?

가격 예측을 표시하기에는 데이터가 부족합니다.

Bristol-Myers Squibb (BRSE:BMY) - 주가, 뉴스 및 분석

BMY 주식 개요

브리스톨-마이어스 스퀴브 컴퍼니는 전 세계에서 바이오 의약품을 발굴, 개발, 허가, 제조, 마케팅, 유통 및 판매하는 기업입니다. 자세한 내용

BMY 기본 분석
눈송이 점수
가치 평가	5/6
미래 성장	4/6
과거 실적	0/6
재무 상태	3/6
배당금	5/6

보상

공정 가치 추정치보다 낮은 67.1% 에서 거래

수익은 매년 49.01% 증가할 것으로 예상됩니다.

동종업계 및 업계 대비 좋은 가치로 거래

위험 분석

주식은 유동성이 매우 낮습니다

부채비율이 높네요

4.85% 의 배당금은 수익으로 잘 충당되지 않습니다.

Bristol-Myers Squibb Company 경쟁사

Novartis

SWX:NOVN

CHF 185.4b

Roche Holding

SWX:ROG

CHF 210.3b

Galderma Group

SWX:GALD

CHF 20.3b

Sandoz Group

SWX:SDZ

CHF 17.1b

가격 내역 및 성능

다음에 대한 모든 사상 최고가, 변동 및 가격 하락 요약 Bristol-Myers Squibb
과거 주가
현재 주가	US$54.24
52주 최고치	US$0
52주 최저치	US$0
베타	0.46
11개월 변경	0%
3개월 변경 사항	0%
1년 변경 사항	0%
33년 변화	22.19%
5년 변화	22.19%
IPO 이후 변화	-0.75%

최근 뉴스 및 업데이트

Recent updates

주주 수익률

	BMY	CH Pharmaceuticals	CH 마켓
7D	0%	-0.7%	-1.1%
1Y	0%	12.3%	8.2%

수익률 대 산업: BMY 지난 1년 동안 12.3 %를 반환한 Swiss Pharmaceuticals 업계보다 저조한 성과를 냈습니다.

수익률 대 시장: BMY 지난 1년 동안 8.2 %를 반환한 Swiss 시장보다 저조한 성과를 냈습니다.

가격 변동성

Is BMY's price volatile compared to industry and market?
BMY volatility
BMY Average Weekly Movement	n/a
Pharmaceuticals Industry Average Movement	3.0%
Market Average Movement	3.2%
10% most volatile stocks in CH Market	6.9%
10% least volatile stocks in CH Market	1.6%

안정적인 주가: BMY 는) 지난 3개월 동안 큰 가격 변동성이 없었습니다.

시간에 따른 변동성: 지난 1년간 BMY 의 변동성 변화를 확인하기에는 데이터가 충분하지 않습니다.

회사 소개

설립	직원	CEO	웹사이트
1887	34,100	Chris Boerner	www.bms.com

브리스톨-마이어스 스퀴브 컴퍼니는 전 세계에서 바이오 의약품을 발견, 개발, 허가, 제조, 마케팅, 유통 및 판매하는 회사입니다. 혈액학, 종양학, 심혈관계, 면역학, 섬유성 및 신경과학 질환을 위한 제품을 제공합니다. 주요 제품으로는 비판막성 심방세동 환자의 뇌졸중/전신색전증 위험 감소 및 심부정맥혈전증/폐색전증 치료를 위한 엘리퀴스, 방광, 혈액, CRC, 두경부암, RCC, 간암, 폐암, 흑색종, MPM, 위암 및 식도암 등 다양한 항암 적응증을 위한 옵디보 등이 있습니다; 다발성 골수종 치료제 포말리스트/이노비드, 활동성 류마티스 관절염 및 건선성 관절염 치료제 오렌시아, 필라델피아 염색체 양성 만성 골수성 백혈병 치료제 스프라이셀 등을 공급하고 있습니다.

Bristol-Myers Squibb Company 기본 사항 요약

Bristol-Myers Squibb 의 수익과 매출은 시가총액과 어떻게 비교하나요?
BMY 기본 통계
시가총액	CHF 84.96b
수익(TTM)	-CHF 5.54b
수익(TTM)	CHF 39.38b

2.2x

P/S 비율

-15.3x

P/E 비율

BMY 주가가 과대평가되어 있나요?

공정 가치 및 가치 분석 보기

수익 및 수익

최신 수익 보고서의 주요 수익성 통계(TTM)
BMY 손익 계산서(TTM)
수익	US$46.51b
수익 비용	US$11.08b
총 이익	US$35.43b
기타 비용	US$41.97b
수익	-US$6.54b

최근 보고된 수익

Jun 30, 2024

다음 수익 날짜

Oct 31, 2024

주당 순이익(EPS)	-3.23
총 마진	76.18%
순이익 마진	-14.06%
부채/자본 비율	306.9%

BMY 의 장기적인 성과는 어땠나요?

과거 실적 및 비교 보기

배당금

4.8%

현재 배당 수익률

-74%

지급 비율

BMY 신뢰할 수 있는 배당금을 지급하나요?

BMY 배당 내역 및 벤치마크 참조

예정된 배당금을 받으려면 언제까지 BMY 을 구매해야 하나요?
Bristol-Myers Squibb 배당 날짜
전 배당일	Oct 04 2024
배당금 지급일	Nov 01 2024
전 배당금까지의 일수	43 days
배당금 지급일까지의 일수	15 days

BMY 신뢰할 수 있는 배당금을 지급하나요?

BMY 배당 내역 및 벤치마크 참조

BMY 주식 개요

보상

위험 분석

Bristol-Myers Squibb Company 경쟁사

SWX:NOVN

CHF 185.4b

SWX:ROG

CHF 210.3b

SWX:GALD

CHF 20.3b

SWX:SDZ

CHF 17.1b

가격 내역 및 성능

최근 뉴스 및 업데이트

Bristol-Myers Squibb Company Showcases the Continued Strength of Its Cardiovascular Portfolio with New Clinical and Real-World Data At American Heart Association Scientific Sessions 2024

Bristol Myers Squibb Presents New Long-Term Data from the EMERGENT Program Evaluating Covenfy in Adults with Schizophrenia At Psych Congress 2024

Bristol Myers Squibb to Present New Clinical and Health Economics and Outcomes Research Data At Psych Congress 2024

U.S. Food and Drug Administration Approves Perioperative Treatment of Neoadjuvant Opdivo® (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Single-Agent Opdivo for Resectable Non-Small Cell Lung Cancer (NSCLC)

Bristol Myers Squibb Presents New Data from Two Trials Demonstrating Sotyktu (Deucravacitinib) Efficacy in Both Moderate-To-Severe Scalp Psoriasis and in A Real-World Setting

U.S. Food and Drug Administration Approves Bristol Myers Squibb's COBENFY (xanomeline and Trospium Chlorx), a First-In-Class Muscarinic Agonist for the Treatment of Schizophrenia in Adults

Recent updates

Bristol-Myers Squibb Company Showcases the Continued Strength of Its Cardiovascular Portfolio with New Clinical and Real-World Data At American Heart Association Scientific Sessions 2024

Bristol Myers Squibb Presents New Long-Term Data from the EMERGENT Program Evaluating Covenfy in Adults with Schizophrenia At Psych Congress 2024

Bristol Myers Squibb to Present New Clinical and Health Economics and Outcomes Research Data At Psych Congress 2024

U.S. Food and Drug Administration Approves Perioperative Treatment of Neoadjuvant Opdivo® (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Single-Agent Opdivo for Resectable Non-Small Cell Lung Cancer (NSCLC)

Bristol Myers Squibb Presents New Data from Two Trials Demonstrating Sotyktu (Deucravacitinib) Efficacy in Both Moderate-To-Severe Scalp Psoriasis and in A Real-World Setting

U.S. Food and Drug Administration Approves Bristol Myers Squibb's COBENFY (xanomeline and Trospium Chlorx), a First-In-Class Muscarinic Agonist for the Treatment of Schizophrenia in Adults

Bristol Myers Squibb Announces New Long-Term Zeposia (ozanimod) Data Demonstrate Durable Efficacy and Consistent Safety in Relapsing Forms of Multiple Sclerosis

Bristol Myers Squibb Presents Landmark 10-Year Follow-Up Data from Checkmate -067 Which Showed Continued Durable Long-Term Survival Benefit with Opdivo® Plus Yervoy® in Advanced Melanoma

Bristol-Myers Squibb Company to Report Q3, 2024 Results on Oct 31, 2024

Bristol Myers Squibb Announces Long-Term Follow-Up Data from Phase 3 Study of CAMZYOS (Mavacamten) Underscores Established Efficacy and Safety Profile in Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM)

Bristol Myers Squibb Receives U.S. Food and Drug Administration sBLA Acceptance for First-Line Treatment of Unresectable Hepatocellular Carcinoma

European Medicines Agency Validates Bristol Myers Squibb's Application for CAR T Cell Therapy Breyanzi for Relapsed or Refractory Follicular Lymphoma

Bristol-Myers Squibb Company Announces Intangible Asset Impairment Charges for the Three Months Ended June 30, 2024

Bristol Myers Squibb Receives European Medicines Agency Validation of Application for Opdivo (Nivolumab) Plus Yervoy (Ipilimumab) for First-Line Treatment of Unresectable or Advanced Hepatocellular Carcinoma

Bristol Myers Squibb Announces U.S. FDA Accelerated Approval of KRAZATI®? (adagrasib) in Combination with Cetuximab for Adult Patients with Previously Treated KRAS G12C-Mutated Locally Advanced or Metastatic Colorectal Cancer (CRC)

Bristol-Myers Squibb Company to Report Q2, 2024 Results on Jul 26, 2024

First quarter dividend of US$0.60 announced

Bristol Myers Squibb Appoints Michael R. McMullen as Independent Director and Member of the Audit Committee, Effective July 1, 2024

Bristol Myers Squibb Declares A Quarterly Dividend, Payable on August 1, 2024

Bristol Myers Squibb Announces Opdivo (Nivolumab) Plus Yervoy (Ipilimumab) Significantly Improved Overall Survival Compared to Lenvatinib or Sorafenib as First-Line Treatment for Patients with Advanced Hepatocellular Carinoma in Checkmate -9DW Trial

Bristol Myers Squibb’S Breyanzi Demonstrates Clinically Meaningful Outcomes Across Broad Range of B-Cell Malignancies in New Data Presented At 2024 Asco® Annual Meeting

U.S. Food and Drug Administration Approves Bristol Myers Squibb’s Breyanzi as a New CAR T Cell Therapy for Relapsed or Refractory Mantle Cell Lymphoma

Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) in Combination with Cisplatin and Gemcitabine

Bristol Myers Squibb Announces New Four-Year Results from the POETYK PSO Long-Term Extension Trial of Sotyktu (Deucravacitinib) Treatment in Adult Patients with Moderate-To-Severe Plaque Psoriasis

Bristol Myers Squibb's CAR T Cell Therapy Breyanzi Approves by the U.S. Food and Drug Administration for Relapsed or Refractory Follicular Lymphoma

Bristol Myers Squibb Provides Update on Phase 3 CheckMate -73L Trial

U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Application for Subcutaneous Nivolumab (nivolumab and hyaluronidase)

European Medicines Agency Validates Bristol Myers Squibb’s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability–High or Mismatch Repair Deficient Metastatic Colorectal Cancer

CHMP Adopts Positive Opinion Recommending Approval of Bristol Myers Squibb's Opdivo (nivolumab) in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma

First quarter 2024 earnings released: US$5.89 loss per share (vs US$1.08 profit in 1Q 2023)

Bristol Myers Squibb Announces KRAZATI (adagrasib) in Combination with Cetuximab Demonstrates Clinically Meaningful Activity as a Targeted Treatment Option for Patients with Previously Treated KRAS G12C-Mutated Locally Advanced or Metastatic Colorectal Cancer (CRC)

U.S. Fda Approves Bristol Myers Squibb and 2Seventy Bio’S Abecma for Triple-Class Exposed Relapsed or Refractory Multiple Myeloma After Two Prior Lines of Therapy

European Commission Expands Approval of Bristol Myers Squibb’S Reblozyl® (Luspatercept)

Bristol Myers Squibb Provides Update on the First Phase 3 YELLOWSTONE Trial Evaluating Oral Zeposia (Oozanimod) in Patients with Moderate to Severe Active Crohn's Disease

Upcoming dividend of US$0.60 per share

Bristol Myers Squibb to Present Data at the American College of Cardiology Annual Scientific Session 2024

Bristol Myers Squibb’s Abecma (idecabtagene vicleucel) Becomes First CAR T Cell Therapy Approved in the European Union in Earlier Lines for Triple-Class Exposed Relapsed and Refractory Multiple Myeloma

Bristol-Myers Squibb Company, Annual General Meeting, May 07, 2024

Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of Karuna Therapeutics, Inc. (NasdaqGM:KRTX) from Capital International Investors, FMR LLC, The Vanguard Group, Inc., T. Rowe Price Group, Inc. (NasdaqGS:TROW) and others.

FDA Advisory Committee Votes in Favor of Bristol-Myers Squibb Company and 2seventy bio, Inc. Abecma for Triple-Class Exposed Multiple Myeloma in Further Lines of Therapy

U.S. FDA Approves Bristol Myers Squibb’s Breyanzi® as the First and Only CAR T Cell Therapy for Adults with Relapsed or Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Bristol-Myers Squibb Company to Report Q1, 2024 Results on Apr 25, 2024

Fourth quarter dividend of US$0.60 announced

U.S. Food and Drug Administration Approves Bristol-Myers Squibb Company's Opdivo

Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of RayzeBio, Inc. (NasdaqGM:RYZB).

Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of RayzeBio, Inc. (NasdaqGM:RYZB).

Bristol Myers Squibb Receives Positive CHMP Opinion for Reblozyl® (luspatercept) for Treatment of Adults with Transfusion-Dependent Anemia due to Low- to Intermediate-Risk Myelodysplastic Syndromes (MDS)

Bristol-Myers Squibb Company Announces Management Changes

U.S. Food and Drug Administration Accepts for Priority Review Bristol Myers Squibb's Application for Augtyro (repotrectinib) for the Treatment of Patients with NTRK-Positive Locally Advanced or Metastatic Solid Tumors

Bristol Myers Squibb Announces Acceptance of U.S. and EU Regulatory Filings for Neoadjuvant Opdivo (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Opdivo in Resectable Non-Small Cell Lung Cancer

Bristol Myers Squibb and 2seventy bio, Inc. Share Update on U.S. FDA Oncologic Drugs Advisory Committee Meeting for Abecma in Triple-Class Exposed Multiple Myeloma Based on KarMMa-3 Study

Full year 2023 earnings released: EPS: US$3.88 (vs US$2.97 in FY 2022)

Bristol-Myers Squibb Company Announces Three Regulatory Acceptances from the U.S. Food and Drug Administration (FDA) and Japan’S Ministry of Health, Labour and Welfare (MHLW) for Breyanzi

Bristol Myers Squibb Announces the First Disclosure of Data from the Phase 3 CheckMate -67T Trial

Bristol-Myers Squibb Company Receives Positive Chmp Opinion for Car T Cell Therapy Abecma (Idecabtagene Vicleucel) in Earlier Lines of Therapy for Triple-Class Exposed Relapsed and Refractory Multiple Myeloma

Bristol Myers Squibb and Exelixis, Inc. Announce Four-Year Follow-Up Results from the CheckMate -9ER Trial Evaluating Opdivo (cabozantinib)

Bristol-Myers Squibb Company (NYSE:BMY) completed the acquisition of Mirati Therapeutics, Inc. (NasdaqGS:MRTX) from a group of shareholders.

Bristol Myers Squibb Announces Results from the Phase 3 Randomized Trial Evaluating Opdivo (nivolumab) Plus Yervoy (ipilimumab)

Bristol Myers Squibb Data At Asco Gu 2024 Showcase Transformative Research in the Treatment of Genitourinary Cancers