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Death, Sudden, Cardiac

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Pipeline Programs
5
Companies
3
Clinical Trials
0
Approved Products

Pipeline by Development Stage

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

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Medtronic
MedtronicNJ - Phillipsburg
2 programs
Defibrillator, Dual Chamber ; ImplantableN/A1 trial
Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study)N/A1 trial
Active Trials
NCT00478933Completed1,223Est. Dec 2012
NCT00664807Completed1,023Est. May 2009
Rhythm Pharmaceuticals
1 program
Defibrillator, Dual Chamber ; ImplantableN/A
Nordic Pharma
Nordic PharmaFrance - Paris
1 program
ECMO resuscitationN/A
Stryker
StrykerCA - San Jose
1 program
ECMO resuscitationN/A1 trial
Active Trials
NCT03700125Completed5Est. Dec 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
StrykerECMO resuscitation
MedtronicMedtronic Genetic Arrhythmia Markers for Early Detection (GAME Study)
MedtronicDefibrillator, Dual Chamber ; Implantable

Clinical Trials (3)

Total enrollment: 2,251 patients across 3 trials

NCT03700125StrykerECMO resuscitation

Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac Arrest. ( SUB30 )

Start: Sep 2019Est. completion: Dec 20225 patients
N/ACompleted
NCT00664807MedtronicMedtronic Genetic Arrhythmia Markers for Early Detection (GAME Study)

Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study)

Start: Apr 2008Est. completion: May 20091,023 patients
N/ACompleted
NCT00478933MedtronicDefibrillator, Dual Chamber ; Implantable

DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients.

Start: Feb 2007Est. completion: Dec 20121,223 patients
N/ACompleted

Phase Legend

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

Key Insights

5 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.