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Cardiac Pacing, Artificial

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Pipeline Programs
3
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
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Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Biotronik
BiotronikGermany - Berlin
2 programs
Implantation of the Solia CSP S pacing lead for LBBAPN/A1 trial
Rate-adaptive pacemaker: accelerometerPHASE_41 trial
Active Trials
NCT06620237Active Not Recruiting152Est. Sep 2027
NCT00323661Completed405Est. Mar 2011
Rhythm Pharmaceuticals
1 program
Medtronic Dual-Chamber PacemakerN/A
Medtronic
MedtronicNJ - Phillipsburg
1 program
Medtronic Dual-Chamber PacemakerN/A1 trial
Active Trials
NCT00422669Terminated205Est. May 2009

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
BiotronikRate-adaptive pacemaker: accelerometer
BiotronikImplantation of the Solia CSP S pacing lead for LBBAP
MedtronicMedtronic Dual-Chamber Pacemaker

Clinical Trials (3)

Total enrollment: 762 patients across 3 trials

NCT00323661BiotronikRate-adaptive pacemaker: accelerometer

Closed Loop Stimulation, Cognitive Performance, and Quality of Life in Pacemaker Patients

Start: May 2006Est. completion: Mar 2011405 patients
Phase 4Completed
NCT06620237BiotronikImplantation of the Solia CSP S pacing lead for LBBAP

BIO|MASTER.CSP Study

Start: Oct 2024Est. completion: Sep 2027152 patients
N/AActive Not Recruiting
NCT00422669MedtronicMedtronic Dual-Chamber Pacemaker

Optimize RV Selective Site Pacing Clinical Trial

Start: Jan 2007Est. completion: May 2009205 patients
N/ATerminated

Phase Legend

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

Key Insights

3 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.