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Dentin Hypersensitivity

1
Pipeline Programs
4
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
0
0
0
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

ViiV Healthcare
ViiV HealthcareNC - Durham
1 program
1
Potassium NitratePhase 2
Solventum
SolventumMN - St. Paul
1 program
3M™ Clinpro™ Fluoride Aqueous SolutionN/A1 trial
Active Trials
NCT05768373Completed101Est. Jul 2023
MTI
MTIUT - Salt Lake City
1 program
Sodium fluoride varnishN/A1 trial
Active Trials
NCT06829277Completed84Est. Jan 2025
GSK
GSKLONDON, United Kingdom
1 program
Potassium NitratePHASE_21 trial
Active Trials
NCT03943095Completed123Est. Aug 2019

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
GSKPotassium Nitrate
MTISodium fluoride varnish
Solventum3M™ Clinpro™ Fluoride Aqueous Solution

Clinical Trials (3)

Total enrollment: 308 patients across 3 trials

NCT03943095GSKPotassium Nitrate

Study to Characterize the Efficacy of a Dual Active Dentifrice for the Relief of Dentin Hypersensitivity

Start: May 2019Est. completion: Aug 2019123 patients
Phase 2Completed
NCT06829277MTISodium fluoride varnish

Evaluation of Biomimetic Mineralization Plus Soft Laser Irradiation in Dentin Hypersensitivity Management

Start: Nov 2024Est. completion: Jan 202584 patients
N/ACompleted
NCT05768373Solventum3M™ Clinpro™ Fluoride Aqueous Solution

A Comparison Study of Hypersensitivity Treatment

Start: Apr 2023Est. completion: Jul 2023101 patients
N/ACompleted

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.