The acute coronary syndrome market is experiencing
significant growth, driven by the increasing prevalence of both
acute myocardial infarction (AMI) and unstable angina, an aging
global population, and advancements in diagnostic technologies.
Innovations in treatment options, such as novel antiplatelet
therapies, personalized medicine, and catheter-based interventions,
are expanding market opportunities. Additionally, rising awareness
and improved healthcare infrastructure, particularly in emerging
markets, are expected to further fuel the growth of the ACS market
in the coming years.
LAS
VEGAS, Jan. 15, 2025 /PRNewswire/ --
DelveInsight's Acute Coronary Syndrome Market Insights
report includes a comprehensive understanding of current treatment
practices, acute coronary syndrome emerging drugs, market share of
individual therapies, and current and forecasted market size from
2020 to 2034, segmented into 7MM [the
United States, the EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan].
Key Takeaways from the Acute Coronary Syndrome Market
Report
- Acute coronary syndrome (ACS) comprises acute myocardial
infarction and Unstable Angina together. The total incidence cases
of ACS in the 7MM were 2.1 million in 2023, of which the
highest incidence cases of this disease were in the United States.
- There are approximately 800,000 incident cases of Acute
Myocardial Infarction (AMI) in the US. These AMI cases contribute
to approximately 60% cases of total ACS cases in the US.
- Almost 75% of ACS patients are males.
- According to DelveInsight's analysis, the market size for acute
coronary syndrome was found to be USD 2.6 billion in the 7MM in 2023.
- Out of all the emerging therapies for ACS, Novo Nordisk's
Ziltivekimab, Idorsia Pharma/Viatris' Selatogrel, and
CellProthera/BioCardia's ProtheraCytes are anticipated to
generate the maximum revenue by 2034.
- The other promising acute coronary syndrome therapies in the
pipeline include Selatogrel (ACT-246475), Dutogliptin,
FARXIGA/FORXIGA (dapagliflozin), FDY-5301, Dalcetrapib (RO4607381),
Vicagrel, Zalunfiban (RUC 4), Ziltivekimab, Milvexian,
ProtheraCytes, KAND567, Olpasiran (AMG 890), Orticumab, and
others.
- The majority of the high- and mid-stage emerging therapies are
small molecules, followed by monoclonal
antibodies, stem cell therapy, and small interfering RNA
(siRNA).
- Leading acute coronary syndrome companies such as
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 are developing novel acute coronary syndrome drugs that
can be available in the acute coronary syndrome market in the
coming years.
- As reported in April 2024,
the EMPACT-MI trial found that JARDIANCE
(empagliflozin) did not significantly reduce the composite risk
of all-cause mortality and heart failure hospitalization in
patients with AMI at increased risk of heart failure when compared
to a placebo.
- In February 2024, CSL
announced top-line results from the Phase III AEGIS-II trial
evaluating the efficacy and safety of CSL112 (apolipoprotein A-I
[human]) compared to placebo in reducing the risk of major adverse
cardiovascular events (MACE) in patients following AMI. The study
did not meet its primary efficacy endpoint of MACE reduction at 90
days. As a result, there are no plans for a near-term regulatory
filing. There were no major safety or tolerability concerns with
CSL112.
Discover which therapies are expected to grab the major acute
coronary syndrome market share @ Acute Coronary Syndrome
Market Report
Acute Coronary Syndrome Overview
Acute coronary syndrome (ACS) is a term used to describe a range
of conditions resulting from the sudden reduction or interruption
of blood flow to the heart. This condition is often caused by the
rupture of an atherosclerotic plaque in the coronary arteries,
leading to blood clot formation and subsequent blockage. The
primary causes of ACS include atherosclerosis, thrombosis, and
spasm of the coronary arteries. Risk factors include hypertension,
high cholesterol, smoking, diabetes, and a sedentary lifestyle.
The symptoms of ACS can range from mild to severe and typically
include chest pain or discomfort, shortness of breath, sweating,
nausea, and dizziness. The chest pain is often described as a
squeezing or pressure-like sensation. In more severe cases, such as
a heart attack (myocardial infarction), symptoms can include
radiating pain to the left arm, jaw, or back.
Diagnosis of ACS is based on clinical presentation,
electrocardiogram (ECG) findings, and blood tests for cardiac
biomarkers such as troponins, which are proteins released into the
blood when the heart muscle is damaged. Imaging techniques,
including coronary angiography, may be employed to visualize the
extent of the blockage and determine the appropriate treatment,
which could range from medication to invasive procedures like
angioplasty or coronary artery bypass grafting (CABG). Early
detection and treatment are crucial in improving outcomes for
patients with ACS.
Acute Coronary Syndrome Epidemiology Segmentation
The acute coronary syndrome epidemiology section provides
insights into the historical and current acute coronary syndrome
patient pool and forecasted trends for the 7MM. It helps recognize
the causes of current and forecasted patient trends by exploring
numerous studies and views of key opinion leaders.
The acute coronary syndrome market report proffers
epidemiological analysis for the study period 2020–2034 in the 7MM
segmented into:
- Total Incident Cases of ACS
- Type-specific Incidence of ACS
- Type-specific Incidence of AMI
- Gender-specific Incidence of ACS
- Treated cases of ACS
Acute Coronary Syndrome Treatment Market
The initial treatment for all cases of ACS includes aspirin (300
mg), a heparin bolus, and an intravenous heparin infusion, provided
there are no contraindications. Antiplatelet therapy with either
ticagrelor or clopidogrel is also recommended, with the choice
depending on the cardiologist's preference. Ticagrelor is not
administered to patients receiving thrombolysis. Supportive care,
such as pain relief with morphine or fentanyl and oxygen for
hypoxia, should be provided as needed. Sublingual or intravenous
nitroglycerin may also be used for pain relief. In cases of
inferior wall ischemia, nitroglycerin can cause significant
hypotension and should be used cautiously. Continuous cardiac
monitoring for arrhythmias is necessary.
Further treatment depends on whether the condition is STEMI,
NSTEMI, or unstable angina. The American Heart Association
recommends urgent catheterization and percutaneous intervention for
STEMI, with a door-to-procedure time of under 90 minutes. If
percutaneous intervention is not available or the patient cannot be
transferred to the catheterization lab in under 120 minutes,
thrombolytics (such as tenecteplase) are advised. The AHA
guidelines suggest the door-to-needle (TNK or other thrombolytic)
time should be under 30 minutes.
With the FDA approval of AGEPHA Pharma's LODOCO, patients
with persistent inflammatory risk now have access to a treatment
specifically designed to lower the risk of cardiovascular disease.
LODOCO works by targeting the inflammatory pathways that contribute
to major cardiac events. The current treatment market is divided
into various therapeutic classes, including antiplatelet agents,
anticoagulants, vasodilators, beta blockers, lipid-lowering drugs,
ACE inhibitors, angiotensin-II receptor blockers (ARBs), and
calcium channel blockers.
To know more about acute coronary syndrome treatment guidelines,
visit @ Acute Coronary Syndrome Management
Acute Coronary Syndrome Pipeline Therapies and Key
Companies
- Selatogrel (ACT-246475): Idorsia Pharmaceuticals and
Viatris
- Dutogliptin: Recardio
- FARXIGA/FORXIGA (dapagliflozin): AstraZeneca
- FDY-5301: Faraday Pharmaceuticals
- Dalcetrapib (RO4607381): DalCor Pharmaceuticals and Roche
- Vicagrel: Jiangsu Vcare PharmaTech
- Zalunfiban (RUC 4): CeleCor Therapeutics
- Ziltivekimab: Novo Nordisk
- Milvexian: Bristol Myers Squibb and Johnson & Johnson
Innovative Medicine
- ProtheraCytes: CellProthera and BioCardia
- KAND567: Kancera
- Olpasiran (AMG 890): Amgen and Arrowhead Pharmaceuticals
- Orticumab: Abcentra
Discover more about acute coronary syndrome drugs in
development @ Acute Coronary Syndrome Clinical
Trials
Acute Coronary Syndrome Market Dynamics
The acute coronary syndrome market dynamics are expected to
change in the coming years. The ACS market is primarily driven by
the increasing prevalence of cardiovascular diseases, rising
geriatric populations, and growing awareness of heart health.
The expanding global burden of risk factors such as hypertension,
diabetes, smoking, and obesity contributes significantly to the
incidence of ACS. Technological advancements in diagnostic
tools, such as high-sensitivity troponin assays and coronary
imaging techniques, have improved early detection and intervention,
driving market growth.
Additionally, the development of novel therapeutic
agents, including anti-platelet therapies, thrombolytics, and
advanced biologics, are further fueling the ACS treatment market.
Healthcare infrastructure improvements, along with rising
healthcare expenditure in emerging markets, also play a crucial
role in expanding access to ACS care. Furthermore, ongoing
research in personalized medicine and the adoption of
minimally invasive procedures are enhancing the overall
treatment landscape, providing a strong boost to market
dynamics.
Furthermore, potential therapies are being investigated for the
treatment of acute coronary syndrome, and it is safe to predict
that the treatment space will significantly impact the acute
coronary syndrome market during the forecast period. Moreover,
the anticipated introduction of emerging therapies and
devices with improved efficacy and a further improvement in
the diagnosis rate are expected to drive the growth of the
acute coronary syndrome market in the 7MM.
However several factors may impede the growth of the acute
coronary syndrome market. One of the primary challenges is the
high cost of treatment, including advanced therapies such as
percutaneous coronary interventions (PCI) and novel drug-based
therapies. These treatments are often expensive, limiting access in
both developing and developed markets. Additionally, the
complexity of diagnosing ACS early and accurately remains a
challenge, with many patients presenting with non-specific
symptoms, leading to delays in treatment and potential
complications.
Regulatory hurdles also present barriers, as
obtaining approvals for new drugs and devices can be time-consuming
and costly. The market is further constrained by the presence of
well-established therapies and the difficulty of demonstrating the
clinical superiority of new treatments. Lastly, patient
adherence to prescribed therapies, lifestyle changes, and the
need for long-term management strategies complicate
treatment outcomes, adding to the burden of ACS.
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 Acute Coronary Syndrome Therapies
|
LODOCO
(colchicine), REPATHA, ZONTIVITY, PRALUENT, Vicagrel, Selatogrel
(ACT-246475), Dutogliptin, FARXIGA/FORXIGA (dapagliflozin),
FDY-5301, Dalcetrapib (RO4607381), Zalunfiban (RUC 4),
Ziltivekimab, Milvexian, ProtheraCytes, KAND567, Olpasiran (AMG
890), Orticumab, and others
|
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 @ 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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Chronic Heart Failure Market
Chronic Heart Failure Market Insights, Epidemiology, and
Market Forecast – 2034 report deliver an in-depth
understanding of the disease, historical and forecasted
epidemiology, as well as the market trends, market drivers, market
barriers, and key CHF companies, including Novartis,
Boehringer Ingelheim, Eli Lilly and Company, Bayer, Cytokinetics,
BioCardia, Novo Nordisk, Mesoblast, among others.
Chronic Heart Failure Pipeline
Chronic Heart Failure Pipeline Insight
– 2024 report provides comprehensive insights
about the pipeline landscape, pipeline drug profiles, including
clinical and non-clinical stage products, and the key CHF
companies, including Zensun (Shanghai) Sci & Tech, Cytokinetics,
Mesoblast, Shanghai Hongyitang Biopharmaceutical Technology, Tasly
Pharmaceuticals, Ionis Pharmaceuticals, Berlin Cures, CardioCell,
Help Therapeutics, Eli Lilly and Company, Chong Kun Dang
Pharmaceutical, Antlia Biosciences, Cardiol Therapeutics, among
others.
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