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Atherosclerotic Cardiovascular Disease

Cardiovascular
11
Pipeline Programs
17
Companies
33
Clinical Trials
6 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
1
1
7
1
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

RNA Therapeutic
1077%
Monoclonal Antibody
215%
Small Molecule
18%
+ 12 programs with unclassified modality

Cardiovascular is a $69.4B mature market dominated by anticoagulants and metabolic therapies with stable blockbuster portfolios.

$69.4B marketMature→ Stable30 products15 companies

Key Trends

  • FXa inhibitors (ELIQUIS, XARELTO) command 62% of market spending, creating limited room for new entrants
  • SGLT2 inhibitors gaining traction in heart failure indication, signaling expansion beyond traditional anticoagulation
  • Multiple patent cliffs (JANUVIA 2027, OPSUMIT 2029) create near-term revenue vulnerability but reinvestment pressure

Career Verdict

Strong choice for commercial, clinical operations, and device integration roles; limited opportunity for innovative pipeline development given market maturity.

AI-generated market analysis based on FDA, CMS, ClinicalTrials.gov, and hiring data

Market Leaders

#1ELIQUISStable
$18.3B
#2JARDIANCEGrowing
$8.8B
#3XARELTOStable
$6.3B
#4FARXIGAGrowing
$4.3B
AstraZeneca·Peak15.3yr
#5JANUVIADeclining
$4.1B
Merck & Co.·LOE_Approaching0.9yr

Drug Class Breakdown

FXa Inhibitors (Apixaban/Rivaroxaban)
$42.8B(62%)

Mature, stable revenue base

SGLT2 Inhibitors
$13.1B(19%)

Growing in heart failure and renal indications

DPP4 Inhibitors
$4.1B(6%)

Declining as LOE approaches 2027

ARBs and Combination Therapies
$3.4B(5%)

Stable in heart failure management

Endothelin Receptor Antagonists and Prostacyclin Agonists
$1.8B(3%)

Niche pulmonary hypertension market

Career Outlook

Stable

Cardiovascular careers are stable but not expanding; the market is mature, dominated by blockbuster franchises with predictable commercial cycles and patent cliffs. Professionals entering this space should expect strong compensation (Commercial $210K avg, Medical Affairs $201K avg) but limited opportunity to drive breakthrough innovation. Device company roles offer better growth trajectories than pharma, particularly in remote monitoring, diagnostics, and patient engagement technologies.

Breaking In

Target device companies (Abbott, Medtronic) for growth potential; if joining pharma, focus on Commercial or Clinical Operations roles where hiring is active and compensation is competitive.

For Experienced Professionals

Leverage cardiovascular expertise to move into medical device strategy, digital health partnerships, or adjacent therapeutic areas; R&D opportunity is limited and may require lateral moves to access innovation-focused roles.

In-Demand Skills

Healthcare economics and payer management (anticoagulation safety monitoring, cost-effectiveness)Real-world evidence generation (postmarket surveillance for FXa inhibitors)Digital health and remote patient monitoring integrationClinical trial execution in large, established patient populationsRegulatory expertise in label expansions (SGLT2 inhibitor indications)

Best For

Commercial/Sales roles (mature market execution)Medical Science Liaisons (managing healthcare provider relationships on established therapies)Clinical Operations/Project Managers (managing large Phase 3/4 programs)Regulatory Affairs (label expansion strategy, patent cliff preparation)Health Economics and Outcomes Research (demonstrating value in competitive anticoagulation market)

Hiring Landscape

$130K-$210K

Cardiovascular hiring is concentrated in device companies (Abbott 337, Medtronic 317) rather than pharma, reflecting the therapeutic area's reliance on hardware solutions and patient management infrastructure. Pharma hiring (Johnson & Johnson 261, Bristol Myers Squibb 52) is heavily weighted toward Commercial (468 roles) and Clinical Operations (296 roles), with minimal R&D investment (14 roles). Medical device integration and remote patient monitoring expertise are increasingly valued as the market consolidates.

1,386
Open Roles
5
Companies Hiring
5
Departments

Top Hiring Companies

337Growing
317Growing

By Department

Commercial(34%)
$210K
Clinical Operations(21%)
$180K
Engineering(13%)
$145K
Medical Affairs(1%)
$201K
Research & Development(1%)
$194K

Device companies offer more growth opportunities; pharma roles are high-paying but oriented toward mature market execution rather than innovation.

Competitive Landscape

14 companies ranked by most advanced pipeline stage

Sandoz
SandozAustria - Kundl
11 programs
1
5
1
InclisiranPhase 4RNA Therapeutic4 trials
InclisiranPhase 3RNA Therapeutic1 trial
InclisiranPhase 3RNA Therapeutic1 trial
InclisiranPhase 3RNA Therapeutic1 trial
Inclisiran sodium 300 mgPhase 3RNA Therapeutic1 trial
+6 more programs
Active Trials
NCT06858332Recruiting2,382Est. Sep 2027
NCT05726838Active Not Recruiting600Est. Mar 2029
NCT05974345Completed204,691Est. Dec 2023
+12 more trials
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
1
AnacetrapibPhase 3
MSD
MSDIreland - Ballydine
1 program
1
AnacetrapibPhase 3
CSL Seqirus
CSL SeqirusUK - Maidenhead
1 program
1
CSL300Phase 2/3
Cyclarity Therapeutics
1 program
1
UDP-003Phase 11 trial
Active Trials
NCT06813339Recruiting84Est. Jun 2027
Novo Nordisk
Novo NordiskBAGSVAERD DENMARK, Denmark
2 programs
No treatment givenN/A1 trial
NNC0385-0434 A 15 mgPHASE_21 trial
Active Trials
NCT07160829Completed608Est. Oct 2025
NCT04992065Completed267Est. Jun 2022
Amgen
AmgenTHOUSAND OAKS, CA
1 program
LpN/A5 trials
Active Trials
NCT07079267Available
NCT06649006Completed6Est. Dec 2025
NCT05489614Completed33Est. Dec 2023
+2 more trials
City Therapeutics
City TherapeuticsMA - Cambridge
1 program
aspirinN/A
Alliance Pharmaceuticals
1 program
aspirinN/A1 trial
Active Trials
NCT02697916Completed15,076Est. Jun 2020
CSL Behring
CSL BehringIL - Bradley
1 program
CSL300PHASE_2_31 trial
Active Trials
NCT05485961Recruiting3,110Est. May 2029
Regeneron
RegeneronTARRYTOWN, NY
1 program
AlirocumabPHASE_3Monoclonal Antibody
Sanofi
SanofiPARIS, France
1 program
AlirocumabPHASE_3Monoclonal Antibody1 trial
Active Trials
NCT01663402Completed18,924Est. Jan 2018
NewAmsterdam Pharma
NewAmsterdam PharmaNARRDEN, Netherlands
1 program
ObicetrapibPHASE_31 trial
Active Trials
NCT05202509Active Not Recruiting9,541Est. Nov 2026
IQVIA
IQVIADURHAM, NC
1 program
Atozet 10/40 mg or 10/80 mgPHASE_41 trial
Active Trials
NCT05761444Completed137Est. Oct 2024

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
SandozInclisiran
IQVIAAtozet 10/40 mg or 10/80 mg
SandozPelacarsen
SandozPelacarsen
NewAmsterdam PharmaObicetrapib
SandozInclisiran sodium 300 mg
SandozInclisiran
SandozInclisiran
SandozInclisiran
SanofiAlirocumab
CSL BehringCSL300
Novo NordiskNNC0385-0434 A 15 mg
AmgenLp
AmgenLp
SandozInclisiran

Showing 15 of 32 trials with date data

Clinical Trials (33)

Total enrollment: 382,041 patients across 33 trials

VictORION-INCLUSION: Evaluating Inclisiran for Cholesterol Managment in Heart Disease

Start: Dec 2024Est. completion: Feb 2027130 patients
Phase 4Active Not Recruiting
NCT05761444IQVIAAtozet 10/40 mg or 10/80 mg

Effectiveness and Safety Study of Early add-on of Ezetimibe With Atorvastatin in Very High-risk Patients

Start: Jul 2023Est. completion: Oct 2024137 patients
Phase 4Completed

An Open Label Extension (OLE) Study (Following Completion of CTQJ230A12301) to Evaluate Long-term Safety and Tolerability of Pelacarsen (TQJ230)

Start: May 2026Est. completion: Jan 20305,700 patients
Phase 3Recruiting

Pelacarsen Roll-over Extension Program

Start: May 2025Est. completion: Dec 2030599 patients
Phase 3Recruiting

Cardiovascular Outcome Study to Evaluate the Effect of Obicetrapib in Patients With Cardiovascular Disease

Start: Feb 2022Est. completion: Nov 20269,541 patients
Phase 3Active Not Recruiting
NCT05030428SandozInclisiran sodium 300 mg

Study of Inclisiran to Prevent Cardiovascular (CV) Events in Participants With Established Cardiovascular Disease

Start: Nov 2021Est. completion: Oct 202717,004 patients
Phase 3Active Not Recruiting

Study in Primary Care Evaluating Inclisiran Delivery Implementation + Enhanced Support

Start: Jul 2021Est. completion: Jan 2023892 patients
Phase 3Completed

A Randomized Study to Evaluate the Effect of an "Inclisiran First" Implementation Strategy Compared to Usual Care in Patients With Atherosclerotic Cardiovascular Disease and Elevated LDL-C Despite Receiving Maximally Tolerated Statin Therapy (VICTORION-INITIATE)

Start: Jun 2021Est. completion: Sep 2023450 patients
Phase 3Completed

A Randomized Trial Assessing the Effects of Inclisiran on Clinical Outcomes Among People With Cardiovascular Disease

Start: Oct 2018Est. completion: Dec 204916,124 patients
Phase 3Active Not Recruiting

ODYSSEY Outcomes: Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab

Start: Oct 2012Est. completion: Jan 201818,924 patients
Phase 3Completed

Combined Dose-Finding and CV Outcomes Study With CSL300 (Clazakizumab) in Adult Subjects With ESKD Undergoing Dialysis (POSIBIL6ESKD)

Start: Oct 2022Est. completion: May 20293,110 patients
Phase 2/3Recruiting
NCT04992065Novo NordiskNNC0385-0434 A 15 mg

A Research Study Looking at How NNC0385-0434 Tablets Work to Lower Blood Cholesterol in People With Heart Disease or a High Risk of Heart Disease

Start: Aug 2021Est. completion: Jun 2022267 patients
Phase 2Completed

Blinatumomab After TCR Alpha Beta/CD19 Depleted HCT

Start: Feb 2021Est. completion: Dec 202925 patients
Phase 2Recruiting

Blinatumomab and Tyrosine Kinase Inhibitor Therapy in People With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia

Start: Mar 2020Est. completion: Mar 202717 patients
Phase 2Active Not Recruiting

An Extension Trial of Inclisiran in Participants With Cardiovascular Disease and High Cholesterol

Start: Apr 2017Est. completion: Dec 2021382 patients
Phase 2Completed

Blinatumomab in Adults With Relapsed/Refractory Philadelphia Positive B-precursor Acute Lymphoblastic Leukemia

Start: Jan 2014Est. completion: Jan 201745 patients
Phase 2Completed

Assessment of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a New Formulation of Inclisiran Containing Polysorbate 80 Compared to the Currently Marketed Formulation

Start: Jun 2026Est. completion: Dec 2026120 patients
Phase 1Not Yet Recruiting

Placebo-controlled Study of Single and Multiple Ascending Doses of UDP-003 in Healthy Human Participants and Patients

Start: Feb 2025Est. completion: Jun 202784 patients
Phase 1Recruiting

Study to Investigate Intravenous Blinatumomab in Japanese Adult Participants With Newly Diagnosed Philadelphia-negative B-precursor Acute Lymphoblastic Leukemia (B-ALL)

Start: Jan 2025Est. completion: Dec 20256 patients
Phase 1Completed

A Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of Olpasiran in Participants With Normal Renal Function and Participants With Various Degrees of Renal Impairment

Start: Sep 2022Est. completion: Dec 202333 patients
Phase 1Completed

A Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of Olpasiran in Participants With Various Degrees of Hepatic Impairment

Start: Sep 2022Est. completion: May 202325 patients
Phase 1Completed

A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Olpasiran in Chinese Participants With Elevated Serum Lipoprotein(a)

Start: Jul 2021Est. completion: Mar 202224 patients
Phase 1Completed

Blinatumomab Consolidation Post Autologous Stem Cell Transplantation in Patients With Diffuse Large B-Cell Lymphoma (DLBCL)

Start: Aug 2017Est. completion: Oct 202314 patients
Phase 1Completed

Olpasiran Expanded Access Program

N/AAvailable

A Real-World Study of Long-Term Adherence and Persistence to Inclisiran, Evolocumab, and Alirocumab

Start: Apr 2026Est. completion: Sep 20265,995 patients
N/ANot Yet Recruiting
NCT07160829Novo NordiskNo treatment given

Focus on Levels of Awareness and Perceptions Regarding hsCRP in Identifying Systemic Inflammation in ASCVD, CKD and Heart Failure Management

Start: Sep 2025Est. completion: Oct 2025608 patients
N/ACompleted
NCT06858332SandozAtorvastatin

Lipoprotein(a) Levels in Patients With Atherosclerotic Cardiovascular Diseases in Russia

Start: Apr 2025Est. completion: Sep 20272,382 patients
N/ARecruiting
NCT05974345SandozInclisiran sodium

In Silico Study Assessing the Impact of Inclisiran on Major Adverse Cardiovascular Events in Patients With Established Cardiovascular Disease

Start: Nov 2023Est. completion: Dec 2023204,691 patients
N/ACompleted
NCT07023445SandozPatterns of Inclisiran Use in the Real World: An Analysis of US Databases

Patterns of Inclisiran Use in the Real World: An Analysis of US Databases

Start: Jan 2023Est. completion: Jun 202437,688 patients
N/ACompleted

A Cross-sectional Study of Lipoprotein(a) Levels in Patients With Documented History of Atherosclerotic Cardiovascular Disease (ASCVD)

Start: Apr 2022Est. completion: Dec 202339,480 patients
N/ACompleted

The Belgian REAL (BE.REAL) Registry

Start: Apr 2022Est. completion: Mar 2029600 patients
N/AActive Not Recruiting

A Non-interventional Implementation Study to Evaluate Treatment With Inclisiran (Leqvio®) and Other Lipid Lowering Treatments in a Real-world Setting

Start: Jan 2022Est. completion: Nov 20251,868 patients
N/ACompleted

Aspirin Dosing: A Patient-Centric Trial Assessing Benefits and Long-term

Start: Apr 2016Est. completion: Jun 202015,076 patients
N/ACompleted

Related Jobs in Cardiovascular

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

7 late-stage (Phase 3) programs, potential near-term approvals
6 actively recruiting trials targeting 382,041 patients
17 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.