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Lateral Ankle Instability

0
Pipeline Programs
2
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

2 companies ranked by most advanced pipeline stage

Stryker
StrykerCA - San Jose
2 programs
Arthrex InternalBraceN/A1 trial
FlexbandN/A1 trial
Active Trials
NCT06829667Completed103Est. Apr 2026
NCT06638138Completed58Est. Dec 2025
Arthrex
ArthrexCA - Santa Barbara
1 program
Modified Brostrum procedure with Internal Brace AugmentationN/A1 trial
Active Trials
NCT04770818Unknown154Est. Mar 2023

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
StrykerArthrex InternalBrace
StrykerFlexband
ArthrexModified Brostrum procedure with Internal Brace Augmentation

Clinical Trials (3)

Total enrollment: 315 patients across 3 trials

NCT06829667StrykerArthrex InternalBrace

Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients Suffering From Lateral Ankle Instability

Start: Oct 2023Est. completion: Apr 2026103 patients
N/ACompleted
NCT06638138StrykerFlexband

Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction of the Anterior Talofibular Ligament (ATFL) to Treat Lateral Ankle Instability

Start: Aug 2023Est. completion: Dec 202558 patients
N/ACompleted
NCT04770818ArthrexModified Brostrum procedure with Internal Brace Augmentation

Lateral Ankle Ligament Reconstruction With InternalBrace™ Augmentation

Start: Mar 2016Est. completion: Mar 2023154 patients
N/AUnknown

Phase Legend

Preclinical— Lab & animal studies
Phase 1— Safety & dosing
Phase 2— Efficacy testing
Phase 3— Large-scale trials
On Market— Approved & available

Key Insights

2 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.