Acute Coronary Syndrome Market To Showcase A Significant Growth At A CAGR Of 7.7% By 2034 Delveinsight
| Acute Coronary Syndrome Market Report Metrics |
Details |
| Study Period |
2020–2034 |
| Coverage |
7MM [the United States, the EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan]. |
| Acute Coronary Syndrome Market CAGR |
7.7 |
| Acute Coronary Syndrome Market Size in 2023 |
USD 2.6 Billion (7MM) |
| Key Acute Coronary Syndrome Companies |
Agepha Pharma, Amgen, Merck, Regeneron and Sanofi, Genentech, Idorsia Pharmaceuticals, Viatris, Recardio, AstraZeneca, Faraday Pharmaceuticals, DalCor Pharmaceuticals, Roche, Jiangsu Vcare PharmaTech, CeleCor Therapeutics, Novo Nordisk, Bristol Myers Squibb, Johnson & Johnson Innovative Medicine, CellProthera, BioCardia, Kancera, Amgen, Arrowhead Pharmaceuticals, Abcentra, and others |
| Key Approved and Emerging |
LODOCO |
Scope of the Acute Coronary Syndrome
Market Report
-
Therapeutic Assessment: Acute Coronary Syndrome
current marketed and emerging therapies Acute Coronary Syndrome
Market Dynamics:
Key Market Forecast Assumptions of Emerging Acute Coronary Syndrome
Drugs and Market Outlook Competitive Intelligence Analysis:
SWOT analysis and Market entry strategies Unmet Needs, KOL's views, Analyst's views, Acute Coronary Syndrome Market Access and Reimbursement
Download the report to understand which factors are driving acute coronary syndrome market trends
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Acute Coronary Syndrome Market Trends
Table of Contents
| 1 |
Key Insights |
| 2 |
Report Introduction |
| 3 |
Executive Summary |
| 4 |
Acute Coronary Syndrome Market Overview at a Glance |
| 4.1 |
Market Share Distribution by Therapies (%) in 2020 in the 7MM |
| 4.2 |
Market Share Distribution by Therapies (%) in 2034 in the 7MM |
| 5 |
Epidemiology and Market Forecast Methodology |
| 6 |
Key Events |
| 7 |
Disease Background and Overview |
| 7.1 |
Introduction |
| 7.2 |
Sign and Symptoms |
| 7.3 |
Risk Factors |
| 7.4 |
Pathogenesis |
| 7.5 |
Classification of ACS |
| 7.6 |
Biomarkers |
| 7.7 |
Diagnosis |
| 7.7.1 |
Differential Diagnosis |
| 8 |
Treatment and Management |
| 8.1 |
Treatment and Management Guidelines |
| 8.1.1 |
AHA/ACC/HFSA Guidelines for the Management of Heart Failure: Executive Summary: 2022 |
| 8.1.2 |
NICE Guidelines for Acute coronary syndromes: 2020 |
| 8.1.3 |
ESC Guidelines for the Management of Acute Myocardial Infarction in Patients Presenting With ST-Segment Elevation: 2017 |
| 8.1.4 |
ESC Guidelines for the Management of Acute Coronary Syndromes (ACS): 2023 |
| 8.1.5 |
ACCF/AHA Guideline for the Management of ST-Elevation Myocardial Infarction |
| 8.1.6 |
Guideline Adherence and Longterm Clinical Outcomes in Patients with AMI in Japan |
| 9 |
Epidemiology and Patient Population of ACS in the 7MM |
| 9.1 |
Key Findings |
| 9.2 |
Assumptions and Rationale |
| 9.3 |
Total Incident Cases of ACS in the 7MM |
| 9.4 |
The United States |
| 9.4.1 |
Total Incident Cases of ACS in the United States |
| 9.4.2 |
Type-specific Incident Cases of ACS in the United States |
| 9.4.3 |
Type-specific Incident Cases of AMI in the United States |
| 9.4.4 |
Gender-specific Incident Cases of ACS in the United States |
| 9.5 |
EU4 and the UK |
| 9.5.1 |
Total Incident Cases of ACS in EU4 and the UK |
| 9.5.2 |
Type-specific Incident Cases of ACS in EU4 and the UK |
| 9.5.3 |
Type-specific Incident Cases of AMI in EU4 and the UK |
| 9.5.4 |
Gender-specific Incident Cases of ACS in EU4 and the UK |
| 9.6 |
Japan |
| 9.6.1 |
Total Incident Cases of ACS in Japan |
| 9.6.2 |
Type-specific Incident Cases of ACS in Japan |
| 9.6.3 |
Type-specific Incident Cases of AMI in Japan |
| 9.6.4 |
Gender-specific Incident Cases of ACS in Japan |
| 10 |
Patient Journey |
| 11 |
Marketed Drugs |
| 11.1 |
Key Cross Competition |
| 11.2 |
LODOCO (colchicine): AGEPHA Pharma |
| 11.2.1 |
Product Description |
| 11.2.2 |
Regulatory Milestones |
| 11.2.3 |
Other Developmental Activities |
| 11.2.4 |
Safety and Efficacy |
| 11.3 |
TNKase (tenecteplase): Genentech |
| 11.3.1 |
Product Description |
| 11.3.2 |
Regulatory Milestones |
| 11.3.3 |
Safety and Efficacy |
| 11.4 |
REPATHA (evolocumab): Amgen |
| 11.4.1 |
Product Description |
| 11.4.2 |
Regulatory Milestones |
| 11.4.3 |
Other Developmental Activities |
| 11.4.4 |
Safety and Efficacy |
| 11.5 |
ZONTIVITY (vorapaxar): Merck |
| 11.5.1 |
Product Description |
| 11.5.2 |
Regulatory Milestones |
| 11.5.3 |
Other Developmental Activity |
| 11.5.4 |
Safety and Efficacy |
| 11.6 |
PRALUENT (alirocumab): Regeneron and Sanofi |
| 11.6.1 |
Product Description |
| 11.6.2 |
Regulatory Milestones |
| 11.6.3 |
Other Developmental Activities |
| 11.6.4 |
Safety and Efficacy |
| 12 |
Other Marketed Assets |
| 12.1 |
Key Cross Competition |
| 12.2 |
INSPRA (eplerenone): Pfizer |
| 12.2.1 |
Product Description |
| 12.2.2 |
Regulatory milestones |
| 12.2.3 |
Safety and efficacy |
| 12.3 |
PLAVIX (clopidogrel bisulfate): Sanofi-Aventis/Bristol-Myers Squibb |
| 12.3.1 |
Product Description |
| 12.3.2 |
Regulatory milestones |
| 12.3.3 |
Other developmental activities |
| 12.3.4 |
Safety and efficacy |
| 12.4 |
BRILINTA/BRILIQUE (ticagrelor): AstraZeneca |
| 12.4.1 |
Product Description |
| 12.4.2 |
Regulatory milestones |
| 12.4.3 |
Safety and efficacy |
| 12.5 |
EFFIENT/EFIENT (prasugrel): Daiichi Sankyo/Eli Lilly and Company |
| 12.5.1 |
Product Description |
| 12.5.2 |
Regulatory milestones |
| 12.5.3 |
Other development activity |
| 12.5.4 |
Safety and efficacy |
| 12.6 |
ATACAND (candesartan): AstraZeneca/Takeda |
| 12.6.1 |
Product Description |
| 12.6.2 |
Regulatory milestones |
| 12.7 |
DIOVAN (valsartan): Novartis |
| 12.7.1 |
Product Description |
| 12.7.2 |
Regulatory milestones |
| 12.7.3 |
Safety and efficacy |
| 13 |
Emerging Therapies |
| 13.1 |
Key Cross Competition |
| 13.2 |
Selatogrel (ACT-246475): Idorsia Pharmaceuticals and Viatris |
| 13.2.1 |
Product Description |
| 13.2.2 |
Other Developmental Activities |
| 13.2.3 |
Clinical Development |
| 13.2.4 |
Safety and Efficacy |
| 13.2.5 |
Analyst View |
| 13.3 |
Dutogliptin: Recardio |
| 13.3.1 |
Product Description |
| 13.3.2 |
Other Developmental Activities |
| 13.3.3 |
Clinical Development |
| 13.3.4 |
Safety and Efficacy |
| 13.3.5 |
Analyst View |
| 13.4 |
FARXIGA/FORXIGA (dapagliflozin): AstraZeneca |
| 13.4.1 |
Product Description |
| 13.4.2 |
Other Developmental Activities |
| 13.4.3 |
Clinical Development |
| 13.4.4 |
Safety and efficacy |
| 13.4.5 |
Analyst View |
| 13.5 |
FDY-5301: Faraday Pharmaceuticals |
| 13.5.1 |
Product Description |
| 13.5.2 |
Other Developmental Activity |
| 13.5.3 |
Clinical Development |
| 13.5.4 |
Safety and Efficacy |
| 13.5.5 |
Analyst View |
| 13.6 |
Dalcetrapib (RO4607381): DalCor Pharmaceuticals and Roche |
| 13.6.1 |
Product Description |
| 13.6.2 |
Other Developmental Activities |
| 13.6.3 |
Clinical Development |
| 13.6.4 |
Safety and Efficacy |
| 13.6.5 |
Analyst View |
| 13.7 |
Vicagrel: Jiangsu Vcare PharmaTech |
| 13.7.1 |
Product Description |
| 13.7.2 |
Other Developmental Activities |
| 13.7.3 |
Clinical Development |
| 13.7.4 |
Analyst View |
| 13.8 |
Zalunfiban (RUC 4): CeleCor Therapeutics |
| 13.8.1 |
Product Description |
| 13.8.2 |
Other Developmental Activities |
| 13.8.3 |
Clinical Development |
| 13.8.4 |
Safety and Efficacy |
| 13.8.5 |
Analyst View |
| 13.9 |
Ziltivekimab: Novo Nordisk |
| 13.9.1 |
Product Description |
| 13.9.2 |
Other Developmental Activities |
| 13.9.3 |
Clinical Development |
| 13.9.4 |
Analyst View |
| 13.10 |
Milvexian: Bristol Myers Squibb and Johnson & Johnson Innovative Medicine |
| 13.10.1 |
Product Description |
| 13.10.2 |
Other Developmental Activities |
| 13.10.3 |
Clinical Development |
| 13.10.4 |
Analyst View |
| 13.11 |
ProtheraCytes: CellProthera and BioCardia |
| 13.11.1 |
Product Description |
| 13.11.2 |
Other Developmental Activities |
| 13.11.3 |
Clinical Development |
| 13.11.4 |
Safety and Efficacy |
| 13.11.5 |
Analyst View |
| 13.12 |
KAND567: Kancera |
| 13.12.1 |
Product Description |
| 13.12.2 |
Other Developmental Activities |
| 13.12.3 |
Clinical Development |
| 13.12.4 |
Safety and Efficacy |
| 13.12.5 |
Analyst View |
| 13.13 |
Olpasiran (AMG 890): Amgen and Arrowhead Pharmaceuticals |
| 13.13.1 |
Product Description |
| 13.13.2 |
Other Developmental Activities |
| 13.13.3 |
Clinical Development |
| 13.13.4 |
Safety and Efficacy |
| 13.13.5 |
Analyst View |
| 13.14 |
Orticumab: Abcentra |
| 13.14.1 |
Product Description |
| 13.14.2 |
Other Developmental Activities |
| 13.14.3 |
Clinical Development |
| 13.14.4 |
Analyst View |
| 14 |
Acute Coronary Syndrome (ACS): 7MM Analysis |
| 14.1 |
Key Findings |
| 14.2 |
Market Outlook |
| 14.3 |
Conjoint Analysis |
| 14.4 |
Key Market Forecast Assumptions |
| 14.5 |
Total Market Size of ACS in the 7MM |
| 14.6 |
United States Market Size |
| 14.6.1 |
Total Market Size of ACS in the United States |
| 14.6.2 |
Market Size of ACS by Therapies in the United States |
| 14.7 |
EU4 and the UK Market Size |
| 14.7.1 |
Total Market Size of ACS in EU4 and the UK |
| 14.7.2 |
Market Size of ACS by Therapies in EU4 and the UK |
| 14.8 |
Japan Market Size |
| 14.8.1 |
Total Market Size of ACS in Japan |
| 14.8.2 |
Market Size of ACS by Therapies in Japan |
| 15 |
Unmet Needs |
| 16 |
SWOT Analysis |
| 17 |
KOL Views |
| 18 |
Market Access and Reimbursement |
| 18.1 |
United States |
| 18.1.1 |
Centre for Medicare and Medicaid Services (CMS) |
| 18.2 |
EU4 and the UK |
| 18.2.1 |
Germany |
| 18.2.2 |
France |
| 18.2.3 |
Italy |
| 18.2.4 |
Spain |
| 18.2.5 |
United Kingdom |
| 18.3 |
Japan |
| 18.3.1 |
MHLW |
| 18.4 |
Reimbursement Scenario and Key HTA Decisions in ACS |
| 19 |
Appendix |
| 19.1 |
Bibliography |
| 19.2 |
Report Methodology |
| 20 |
DelveInsight Capabilities |
| 21 |
Disclaimer |
| 22 |
About DelveInsight |
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