Biotronik
Biotronik sponsors 30 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 20 completed. 5 of these trials are in Phase 3-4 (later-stage) and 4 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Bradycardia, with 2 trials.
Trial Pipeline
30 total, page 1 of 1
BIOTRONIK Investigation of the LivIQ Leadless Pacemaker System
NCT07118358
BIOTRONIK Conduction System Pacing With the Solia Lead - Solia CSP S
NCT06540079
BIOTRONIK Conduction System Pacing With the Solia Lead
NCT05251363
Atrial Fibrillation Associated With Heart Failure Treated by BIOTRONIK's CRT-DX System
NCT04870281
Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions
NCT04175626
Assessment of the Utility of BIOMONITOR to Identify Atrial Fibrillation (AF) in Ablation Candidates Using Precise AF Detection
NCT04076917
Analysis of Both Sex and Device Specific Factors on Outcomes in Patients with Non-Ischemic Cardiomyopathy
NCT03884608
Comparison of the Effects of Two Spinal Cord Stimulation (SCS) Therapies on Subject Reported Pain (BENEFIT-02)
NCT03594266
QP ExCELs: MultiPole Pacing (MPP) Sub-Study
NCT03155724
Plexa ICD Lead Registry
NCT03103503
BioMonitor 2 In-Office Setting Insertion Safety and Feasibility Evaluation With Device Functionality Assessment
NCT02756338
Safety and Effectiveness of the Orsiro Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery Lesions
NCT02389946
Protego DF4 Post Approval Registry
NCT02243696
ProMRI Study of the Iforia ICD System (Phase C)
NCT02096692
ProMRI Study of the Entovis Pacemaker System (Phase B)
NCT02009696
Safety and Performance Study of the Siello S Pacing Lead
NCT01791127
ProMRI Study of the Entovis Pacemaker System
NCT01761162
BIOHELIX-I Bare Metal Stent Study
NCT01612767
Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents
NCT01319812
Long-term Evaluation of the Linox Family ICD Leads Registry (GALAXY)
NCT00836589
Post Approval Registry of Corox OTW, Endocardial, Left Ventricular Steroid Lead, Bipolar
NCT00810264
Echocardiography Guided Cardiac Resynchronization Therapy (EchoCRT)
NCT00683696
Combined Use of BIOTRONIK Home Monitoring and Predefined Anticoagulation to Reduce Stroke Risk
NCT00559988
REPLACE: Implantable Cardiac Pulse Generator Replacement Registry
NCT00395447
Interventricular Delay of Lumax HF-T for Heart Failure
NCT00508391
TRIAGE-CRT Telemonitoring in Patients With CHF and Indication of CRT-D
NCT00395642
COSMO Post Approval Registry: Corox OTW Steroid LV Lead Monitoring
NCT00396136
Effectiveness of Pacemaker With Closed Loop Stimulation Compared to Pacemakers With and Without Standard Rate Response
NCT00355797
TRUST: Lumos-T Safely RedUceS RouTine Office Device Follow-up
NCT00336284
Investigational Device Exemption (IDE) Study for the Approval of Closed Loop Stimulation (CLS) and Cardiac Resyncronization Pacing Therapies (CRT) for the Treatment of Atrial Fibrillation (AF) With Ablate and Pace
NCT00356057
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 2 | 4 |
| Phase 4 | 5 |
What the Pipeline for Biotronik Shows
According to the ClinicalTrials.gov registry, Biotronik is linked to 30 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 3% of the sponsor's indexed portfolio, and 20 are already marked complete, representing roughly 67% of the total.
The phase mix for Biotronik reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 4 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Biotronik is Bradycardia with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.