❤️
Cardiovascular
Therapies for heart disease, stroke, and vascular conditions including novel lipid-lowering and anti-thrombotic agents.
Companies
0
Pipeline Drugs
2016
Key People
2227
Cardiovascular Pipeline (2016 drugs)
Commercial: 378Pre-clinical: 226Approved: 118Preclinical: 115Phase 3: 107Development: 91Phase 2: 79Phase 1: 68Research: 40Marketed: 31Phase III: 29Post-Market: 16Phase 1/2: 16Not Specified: 14Pivotal: 13Discovery: 13Launched: 12Pivotal Trial: 11Research/Development: 11Early-stage Clinical: 11Phase II: 10Unknown: 10Phase 2/3: 9Development/Commercial: 9Not Disclosed: 8Phase I: 8Pre-clinical/Development: 7Investigational: 7Clinical: 6Various: 6Phase1: 6Phase 2b: 5Clinical Development: 5Commercial Launch: 5ANDA Approved: 5Feasibility: 5Early Feasibility: 5Pre-clinical/Clinical: 5Development/Validation: 5Phase I/II: 5ANDA Filed/Approved: 5Marketed (Global): 5Under Development: 4Regulatory Submission: 4Clinical Research: 4Pre‑clinical: 4N/A: 4Regulatory Review: 4Commercial Model: 4Clinical Validation: 4Commercial/Development: 4Clinical Trials: 4Clinical Evidence: 4Phase 2A: 4Randomized Controlled Trial: 3Post-Market Registry: 3Observational Study: 3Discovery/Development: 3Phase 2a: 3Early Development: 3Platform/Tool Development: 3Approved/Commercial: 3Commercial (CE Mark): 3NA: 3Service Offering: 3Commercial Development: 3Early Feasibility Study: 3Research/Preclinical Tools: 3RUO Kit: 3Clinical Study: 3Phase 2B/3: 3Not Disclosed (Sponsor-led): 3Regulatory: 3Discovery/Validation: 3Commercial (Iterative Development): 3Phase 4: 3Discovery/Preclinical: 3Research/Pre‑clinical: 3Approved / Lifecycle: 3Clinical Investigation: 3Human Clinical: 3commercial: 2Design & Development: 2Filed: 2Research/Discovery: 2Phase IIb/III: 2R&D: 2Pre-clinical/Feasibility: 2Pivotal Study: 2Pre-Clinical: 2Commercial/Diagnostic: 2Implementation: 2Phase 1b/2a: 2FDA-Cleared: 2Various (Typically Phase 2-4): 2Commercial (Post-market): 2Registry: 2Phase 3 (IDE): 2Pre-market: 2Strategic Development: 2Technology Development: 2Pre-commercial: 2Research/Preclinical: 2Commercial (Ongoing Development): 2Clinical Trial: 2Feasibility / First-in-Human: 2Commercial Deployment: 2Pre-launch: 2First-in-Human: 2Development/ANDA Filing: 2Research/Pre-clinical: 2Clinical Stage (Phase not specified): 2Commercial Expansion: 2Pre-clinical (inferred): 2Early Research: 2Feasibility Study: 2Phase2: 2Pre-clinical/Planning: 2Phase 1b: 2Pre-clinical / Early Clinical: 2Early Clinical: 2Research/Validation: 2Cleared: 2Clinical Feasibility: 2Preclinical to Commercial: 2Phase 1/2a: 2Commercial (RUO): 2Phase 3/4: 2Discovery/Optimization: 2Pre-approval: 2Development/Marketed: 2Clinical-stage (phase unspecified): 2Commercial (licensed): 2Phase 2 (Observational Clinical Study): 2Regulatory Approved: 2Approved / Phase III: 2Phases I-III & Commercial: 2Development & Commercial: 2Preclinical/Discovery: 2Phase II/III: 2FDA Approved: 2Completed: 2Commercial / Ongoing Research: 2Various (Partner-led): 2Pre-market (NMPA under review): 2Phase 3-ready: 2pre‑clinical: 1Marketed / NDA: 1ANDA / Marketed: 1Research / Pre-clinical: 1Application Submitted / BE Stage: 1Preclinical/Exploratory: 1Concept / Early Development: 1ANDA Filed / Development: 1ANDA Pending / Development: 1Marketed / Line Extensions: 1Market Launch: 1PMA Supplement: 1Development & Expansion: 1Assay Menu Expansion: 1Integrated Solution: 1Solution: 1FDA Approved / PMA: 1Pivotal Study (U.S.): 1Not Disclosed (Likely Preclinical/Early Clinical): 1NDA Submitted: 1Approved (Japan): 1Commercial (in China): 1IND-Enabling: 1Phase I-III: 1Phase IV: 1Commercial (China/EU) / Clinical (US): 1Safety & Effectiveness Study: 1Investigational Study: 1Feasibility Trial: 1Randomized Controlled Study: 1Approved / Marketed: 1Discovery / Preclinical: 1Development/Commercial (LDT): 1Next-Generation Development: 1Commercialization: 1Early Exploration: 1FDA Breakthrough Device Designation: 1Screening/Diagnostic: 1Various (Typically Phase 3): 1Early-Stage (FIH/EFS): 1Early Clinical Development: 1First-in-Human (FIH): 1Platform Technology: 1Approved (CE-IVD): 1Phase-3: 1Phase-2: 1Approved (India): 1Clinical-Stage: 1Development/ANVISA Submission: 1Pre-clinical/Concept: 1Unspecified: 1Pre-clinical / Early Feasibility: 1Phase 1-3: 1Research-Use Only: 1Pre-clinical/R&D: 1Breakthrough Device Designation / Commercial: 1Approved (510(k)): 1ANDA Filed/Pre-approval: 1Concept through Development: 1Phase 2/Phase 3: 1Pre-clinical / Early Development: 1Pre-clinical / Concept: 1Development/Regulatory Review: 1Launching: 1Pivotal Trial Completed: 1ANDA Filed/Development: 1IVD Kit: 1First-in-Human / Early Feasibility: 1Investigational / Pre-clinical: 1Development/NDA Filing: 1Development/DMF Submission: 1Pre-clinical / Phase 1 (BA/BE): 1Product Launch: 1Commercial Integration: 1Development/Commercialization: 1Ongoing Development: 1Pre-clinical/Discovery: 1Approved/Commercial (Limited): 1Pivotal Trial Preparation: 1Pre-clinical/Investigational: 1Commercial / PMA Supplement: 1Development / Clinical: 1Pivotal Trial Planning: 1Phase 3 (planned): 1Phase 2 (planned): 1Commercial (EU); Investigational (US): 1Development/Construction: 1Approved (Breakthrough Device): 1Commercial / Generic Development: 1Commercial Launch (EU): 1ANDA Development/Filing: 1Phase 1 / Bioequivalence: 1Investigational / Pivotal Trial: 1Development/Pre-clinical: 1Phase 2B: 1Device Development: 1Clinical Study Completed: 1Early Feasibility / Investigational: 1Feasibility / Early Clinical: 1Development/Regulatory Clearance: 1Commercial Enhancement: 1Post-Market Studies: 1Early Clinical Investigation: 1Pre-clinical/Phase 1: 1Phase 1/Preclinical: 1Pivotal IDE Trial: 1Pivotal IDE: 1Development/Registration: 1N/A (Observational/Mechanistic): 1N/A (Registry): 1Pilot: 1Pilot Observational Study: 1Pre-clinical/Clinical Study: 1IDE Clinical Trial: 1IND Cleared: 1Pre-clinical / Planning: 1First-In-Human (FIH): 1Pilot Study: 1Clinical Stage: 1CE Mark Trial: 1Pilot Studies: 1N/A (Clinical Research Trial): 1Development/Manufacturing: 1Concept to Commercialization: 1Production: 1Pivotal Trial (Planned): 1Research & Development: 1Assay Development: 1Launch/Commercialization: 1Pre-market Approval (FDA Breakthrough): 1Pre-clinical / Feasibility: 1Pre-clinical Trial: 1Early Feasibility / First-in-Human: 1Ongoing R&D: 1Research/Clinical Validation: 1Early Feasibility Study (First-in-Human): 1Development/Commercial Expansion: 1Pre-clinical/Clinical Investigation: 1Not Disclosed (Likely Pre-clinical/Early Clinical): 1Commercial/Research: 1Phase IIb: 1IND filed: 1Pre-clinical/Research: 1Registration/Clinical: 1Pivotal Trial (IDE): 1Pivotal study planned: 1Pivotal/Pre-market: 1Bioequivalence/Registration: 1Post-Market Study: 1Pre-market Clinical Research: 1Regulatory Review (NMPA Green Path): 1CE Mark Obtained; NMPA Green Path: 1NMPA Approved: 1Registration: 1Discovery/Lead Optimization: 1Service: 1Phase 3 / Registration: 1Phase 1/Phase 2: 1Clinical Development (phase unspecified): 1Development/Pre-market: 1Conditionally Approved: 1Research Tool: 1Commercial (cleared): 1IND Accepted: 1NDA: 1IND: 1Market: 1Not Specified (Commercial/Registration): 1Filed/Phase III: 1Preclinical/Phase I: 1Multiple (I-III): 1Development/Clinical Trials: 1Filed/Approved: 1Development/Filed: 1Phase III / Marketed: 1Approved/Phase III: 1Application Submitted: 1BE Studies / Scale-up: 1Preclinical / Early Development: 1Formulation Development: 1CE Mark / FDA Clearance (Ongoing): 1PMA Under Review: 1Commercial / Development: 1ANDA Tentative Approval: 1Process Validation: 1Clinical/Commercial: 1NDA Resubmitted: 1Marketed/Development: 1Commercial & Development: 1Commercial & Line Extensions: 1Early Feasibility/Pivotal: 1Phase IV / Post-Marketing: 1Various Clinical Trials: 1Pre-clinical / Clinical Research: 1Phase III / NDA: 1Phase II / Phase III: 1Phase I / Phase II: 1ANDA Submitted: 1Marketed (ex-US): 1Partnership: 1Phase not specified (Class 1 New Drug): 1Not specified (API/Formulation): 1Discovery to Clinical: 1Preclinical Research: 1Product Development: 1Market Expansion: 1Launch Preparation: 1Clinical Use: 1Not Applicable: 1Phase 1b/2: 1Global Clinical Trial: 1Pre-market (NMPA approved 2025): 1Research/Commercial: 1Approved (China NMPA Review): 1Commercial (CE Mark) / Pivotal Trial (US): 1Investigational / Early Commercial: 1Clinical-stage: 1
| Drug | Company | Indication | Phase |
|---|---|---|---|
| Xolatryp | Nyrada | Cardioprotection (STEMI) and Neuroprotection (stroke, TBI) | Phase 1 |
| PCSK9 inhibitor | Nyrada | Hypercholesterolemia (statin‑resistant) | Preclinical |
| Peripheral nerve pain agent | Nyrada | Neuropathic pain | Preclinical |
| Autoimmune psoriasis candidate | Nyrada | Psoriasis | Preclinical |
| EndoForce™ Connector | Phraxis | Endovascular venous anastomosis for arteriovenous graft (AVG) implantation in hemodialysis access | Approved |
| Epi+Gen CHD™ | Cardio Diagnostics Holdings | Risk Assessment for Obstructive Coronary Heart Disease | Commercial |
| PrecisionCHD™ | Cardio Diagnostics Holdings | Diagnosis of Obstructive Coronary Heart Disease | Development |
| Cardiac Cell Therapy Program | StemCardia | Heart Failure | Pre-clinical |
| Stem Cell Therapy for Blood Diseases | GIOSTAR | Sickle Cell Anemia, Leukemia, Lymphoma, Thalassemia | Not Disclosed |
| Stem Cell Therapy for Type 1 Diabetes | GIOSTAR | Diabetes (Type 1) | Under Development |
| Stem Cell Therapy for Neurodegenerative Diseases | GIOSTAR | Alzheimer’s, Parkinson’s, ALS, Multiple Sclerosis | Under Development |
| Stem Cell Therapy for Autoimmune Diseases | GIOSTAR | Lupus, Crohn's, Vasculitis, Scleroderma | Under Development |
| FastWave Artero | Fastwave Medical | Peripheral Artery Disease (PAD) - calcific lesions | Pre-clinical |
| FastWave Sola | Fastwave Medical | Coronary Artery Disease (CAD) - calcific lesions | Pre-clinical |
| ART001 | AccurEdit Therapeutics | ATTR (Transthyretin Amyloidosis) | Phase 1 |
| dl-3-n-Butylphthalide (NBP) Soft Capsules | cspc-pharmaceutical | Ischemic Stroke | Phase 3 |
| Benzonatate Soft Capsules | cspc-pharmaceutical | Cough Suppressant | Commercial |
| Azithromycin Preparations | cspc-pharmaceutical | Bacterial Infections | Commercial |
| Penem Preparations | cspc-pharmaceutical | Bacterial Infections | Commercial |
| Various Penicillin/Cephalosporin Products | cspc-pharmaceutical | Bacterial Infections | Commercial |
| PhysioWave Pro™ | Physiowave | Arterial stiffness / cardiovascular risk assessment | commercial |
| PhysioWave X | Physiowave | Cardiovascular risk stratification, emergency department intake | commercial |
| PhysioWave Home | Physiowave | Remote home monitoring of PWV and vital signs | pre‑clinical |
| Hypertension Pharmacogenomic Test | Geneticure | Treatment guidance for hypertension | Commercial |
| Rapid Diagnostic Test Platform | ZiJian Biotechnology | Infectious Disease Screening | Commercial |
| Portable Analyzer Device | ZiJian Biotechnology | Chronic Disease Monitoring | Commercial |
| ESNtx005 | ESN cleer | Rare Cardiomyopathy | Preclinical |
| TCM Product Portfolio | China SXT Pharmaceuticals | Cardiovascular, Digestive, Metabolic Disorders | Marketed / NDA |
| Generic Drug Portfolio | China SXT Pharmaceuticals | CNS, Cardiovascular, Anti-infective | ANDA / Marketed |
| New TCM Formulations | China SXT Pharmaceuticals | Not Specified | Research / Pre-clinical |
| New Generic Approvals | China SXT Pharmaceuticals | Various | Application Submitted / BE Stage |
| SofPulse® | Endonovo Therapeutics | Post-operative Pain & Edema | Commercial |
| Electroceutical® Therapy | Endonovo Therapeutics | Ischemic Heart Disease | Preclinical/Exploratory |
| Polymer Sealed Vascular Grafts | RUA Medical | Large Bore Vascular Repair (e.g., Aortic) | Design & Development |
| Soft Tissue Patches | RUA Medical | Surgical Repair | Design & Development |
| Polymeric Tri-leaflet Heart Valve | RUA Medical | Heart Valve Replacement | Concept / Early Development |
| Authorized Generic of Nucynta® ER (tapentadol) | hikma | Pain Management | Launched |
| Authorized Generic of Nucynta® (tapentadol) | hikma | Pain Management | Launched |
| Complex Generic Injectables Portfolio | hikma | Various (Oncology Support, Anti-infectives, CNS) | ANDA Filed / Development |
| Oral Solid Dose Generics Portfolio | hikma | Various (CV, CNS, Diabetes) | ANDA Pending / Development |
| Branded Specialty Portfolio (MENA) | hikma | Oncology, Diabetes, Cardiovascular, Respiratory | Marketed / Line Extensions |
| MultiStem | Athersys | Ischemic Stroke | Phase 3 |
| Elyea (relugolix combo) | Organon (2) | Heavy Menstrual Bleeding with Uterine Fibroids; Endometriosis Pain | Approved |
| Phexxi | Organon (2) | Non-hormonal Contraceptive | Approved |
| Orilissa (elagolix) | Organon (2) | Endometriosis Pain | Approved |
| Biosimilar Aflibercept | Organon (2) | Ophthalmology (nAMD, DME) | Filed |
| Biosimilar Denosumab | Organon (2) | Osteoporosis, Bone Metastasis | Phase 3 |
| Biosimilar Ranibizumab | Organon (2) | Ophthalmology (nAMD, DME, RVO) | Phase 3 |
| Biosimilar Ustekinumab | Organon (2) | Plaque Psoriasis, Psoriatic Arthritis, IBD | Phase 3 |
| Biosimilar Bevacizumab | Organon (2) | Oncology | Phase 3 |
Key People in Cardiovascular
JM
John Moore
Non‑Executive Chair
Nyrada
JB
James Bonnar
CEO
Nyrada
BE
Benny Evison
Chief Scientific Officer
Nyrada
AY
Alex Yevzlin, MD
Chief Executive Officer, Co-Founder and Director
Phraxis
JZ
John Zentgraf
Chief Operating Officer, Co-Founder and Director
Phraxis
GB
Geoff Beecher
Chief Commercial Officer
Phraxis
LP
Leota Pearson
Chief Financial Officer
Phraxis
CM
Chuck Murry, MD, PhD
Co-Founder, Pioneer in Heart Regeneration
StemCardia
LP
Lil Pabon, PhD
Co-Founder
StemCardia
CC
Carter Cliff
Co-Founder, CEO
StemCardia
RM
Robb MacLellan, MD
Advisor, Heart Failure Clinician-Scientist
StemCardia
DA
Dr. Anand Srivastava
Chairman and Founder
GIOSTAR
DE
Dr. Eleanor Vance
CEO
ClotProtect
DR
Dr. Rajiv Mehta
CSO
ClotProtect
YW
Yongzhong Wang, Ph.D.
Founder, Chairman and CEO
AccurEdit Therapeutics