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Cervical Spondylosis

1
Pipeline Programs
7
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

6 companies ranked by most advanced pipeline stage

Pfizer
PfizerNEW YORK, NY
1 program
1
PregabalinPhase 41 trial
Active Trials
NCT01061697Completed50Est. Apr 2010
Providence Medical Technology
1 program
DTRAX GraftN/A
Providence Therapeutics
1 program
DTRAX GraftN/A1 trial
Active Trials
NCT01616719Withdrawn0Est. Feb 2015
NuVasive
NuVasiveCA - San Diego
1 program
NuVasive® ACP System StudyN/A
Globus Medical
Globus MedicalAUDUBON, PA
1 program
NuVasive® ACP System StudyN/A1 trial
Active Trials
NCT05066711Enrolling By Invitation75Est. Jun 2027
Spine BioPharma
Spine BioPharmaNY - New York
1 program
ViviGenN/A1 trial
Active Trials
NCT02814825Completed100Est. Apr 2021

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
PfizerPregabalin
Globus MedicalNuVasive® ACP System Study
Spine BioPharmaViviGen
Providence TherapeuticsDTRAX Graft

Clinical Trials (4)

Total enrollment: 225 patients across 4 trials

Pregabalin and Radicular Pain Study (PARPS)

Start: Jan 2008Est. completion: Apr 201050 patients
Phase 4Completed
NCT05066711Globus MedicalNuVasive® ACP System Study

NuVasive® ACP System Study

Start: May 2022Est. completion: Jun 202775 patients
N/AEnrolling By Invitation

An ACDF Multi-Center Study Using ViviGen Cellular Bone Matrix

Start: Jun 2016Est. completion: Apr 2021100 patients
N/ACompleted

Evaluation of DTRAX Graft in Patients With Cervical Degenerative Disc Disease

Start: May 2012Est. completion: Feb 20150
N/AWithdrawn

Phase Legend

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

Key Insights

7 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.