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Arteriovenous Fistula Stenosis

0
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
0
0
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Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Acotec
AcotecChina - Beijing
2 programs
drug-coated balloon catheter (Orchid, Acotec)N/A1 trial
paclitaxel-coated balloon catheterN/A
Active Trials
NCT03366727Completed244Est. Jul 2022
Medtronic
MedtronicNJ - Phillipsburg
1 program
IN.PACT AV DCBN/A1 trial
Active Trials
NCT03041467Completed330Est. May 2023
Boston Scientific
Boston ScientificCA - Valencia
1 program
RANGER™ Paclitaxel Coated Balloon CatheterN/A1 trial
Active Trials
NCT06639451Active Not Recruiting186Est. Dec 2026

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Boston ScientificRANGER™ Paclitaxel Coated Balloon Catheter
Acotecdrug-coated balloon catheter (Orchid, Acotec)
MedtronicIN.PACT AV DCB

Clinical Trials (3)

Total enrollment: 760 patients across 3 trials

NCT06639451Boston ScientificRANGER™ Paclitaxel Coated Balloon Catheter

A Prospective, Multi-center Study to Evaluate Efficacy and Safety of BSJ020R in Treatment of AVF for Hemodialysis (RANGER AV Japan Study)

Start: Dec 2024Est. completion: Dec 2026186 patients
N/AActive Not Recruiting
NCT03366727Acotecdrug-coated balloon catheter (Orchid, Acotec)

AcoArt III / Arterio-venous Fistula in China

Start: May 2018Est. completion: Jul 2022244 patients
N/ACompleted
NCT03041467MedtronicIN.PACT AV DCB

IN.PACT™ AV Access IDE Study

Start: Apr 2017Est. completion: May 2023330 patients
N/ACompleted

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.