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Plantar Fasciitis

1
Pipeline Programs
4
Companies
4
Clinical Trials
0
Approved Products

Pipeline by Development Stage

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

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Zimmer Biomet
Zimmer BiometFL - Jacksonville
1 program
1
L-PRP InjectionPhase 41 trial
Active Trials
NCT00758641Completed115Est. Jan 2016
Globus Medical
Globus MedicalAUDUBON, PA
1 program
Amnios™ RTN/A1 trial
Active Trials
NCT04088383Completed150Est. Nov 2022
Sound Pharmaceuticals
1 program
Custom PFON/A1 trial
Active Trials
NCT01882894Unknown60Est. Dec 2014
Mission Therapeutics
Mission TherapeuticsUK - Cambridge
1 program
dorsiflexion night splintPHASE_41 trial
Active Trials
NCT00222911Completed75Est. Nov 2006

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Zimmer BiometL-PRP Injection
Mission Therapeuticsdorsiflexion night splint
Globus MedicalAmnios™ RT
Sound PharmaceuticalsCustom PFO

Clinical Trials (4)

Total enrollment: 400 patients across 4 trials

Platelet Rich Plasma to Treat Plantar Fasciitis

Start: Sep 2009Est. completion: Jan 2016115 patients
Phase 4Completed
NCT00222911Mission Therapeuticsdorsiflexion night splint

Treatment of Plantar Fasciitis With Dorsiflexion Night Splints and Medial Arch Supports

Start: Aug 2005Est. completion: Nov 200675 patients
Phase 4Completed

Amnios™ RT Outcomes Study

Start: Sep 2019Est. completion: Nov 2022150 patients
N/ACompleted

Efficacy of a Custom Temporary Foot Orthosis for Plantar Fasciitis Treatment

Start: Sep 2013Est. completion: Dec 201460 patients
N/AUnknown

Phase Legend

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

Key Insights

4 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.