Procter and Gamble
Procter and Gamble sponsors 70 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 65 completed. 12 of these trials are in Phase 3-4 (later-stage) and 11 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Gingivitis, with 5 trials.
Trial Pipeline
70 total, page 1 of 2
Assessing Gingivitis and Plaque From a Marketed Toothpaste
NCT07158112
Evaluating Gingivitis and Systemic Biomarkers
NCT06962956
A Clinical Study to Assess the Gingivitis and Plaque Effects of Various Dentifrices
NCT06140784
Stannous Fluoride and Gingivitis
NCT05326373
A Meta-analysis Comparing Toothbrushes on Plaque Removal and Gingival Health
NCT05594004
Brief Title: a Clinical Study to Assess Gingivitis
NCT06659471
Overnight Pant Study for Children With Nocturnal Enuresis
NCT05178641
A Three Month Bleeding-Model Clinical Study
NCT05916521
A Clinical Study to Assess the Gingivitis Effects of Various Dentifrices
NCT06140771
Salivary Fluoride Clearance
NCT06735235
Measuring Efficacy of an Oral-Irrigator After Three Weeks of Use
NCT04899440
Assessing Effects of a Denture Gel on Gum Abrasions
NCT04913636
Evaluation of the Fluoride Dose Response Using In Situ Caries Model
NCT04763044
A Bleeding-Model Clinical Study
NCT05916508
Improvement of Dry Mouth Sufferers After Using an Experimental Dry Mouth Rinse Compared to a Water Control
NCT04189081
A Pilot Study to Assess Dry Mouth Relief After Using an Experimental Mouth Rinse
NCT04152642
A Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity
NCT03965039
A Study to Determine the Efficacy of a Denture Adhesive to Seal Out Food Particles From Under the Mandibular Partial Denture
NCT05908890
A Clinical Study to Assess the Plaque and Gingivitis Effects of a Stannous Fluoride Dentifrice
NCT03936569
In-use Cross-over Study of Two Different Menstrual Cups
NCT05411796
Evaluate Dental Plaque Benefit of a Preventive Treatment Gel
NCT03546491
A Clinical Study to Assess the Effects of a Stannous Fluoride Dentifrice on Plaque and Gingivitis
NCT03936556
In-use Study of Four Different Tampons
NCT03478371
Meta-analysis of Stannous Fluoride Dentifrice and the Effects on Dentine Hypersensitivity
NCT04005417
Meta-analysis of Stannous Fluoride and the Effects on Dental Plaque
NCT04006483
Meta-analysis of Stannous Fluoride and the Effects on Enamel Erosion
NCT04006470
The Effects of Oscillating-Rotating Electric Toothbrushes on Plaque and Gingival Health
NCT04017507
Meta-analysis of Stannous Fluoride and the Effects on Gingival Health
NCT03970759
8-Week Atopic Dermatitis (AD) Treatment Study
NCT03386032
Analysis of Stannous Fluoride in GCF and Subgingival Plaque
NCT03296657
A Follow-Up Survey of Oral Hygiene and Health Outcomes for Women Previously Enrolled in "OHMOM"
NCT02922010
Research on Oral Tolerability and Product Application/Response of Two Oxalate Products for Dental Patients With Risk of Dentinal Hypersensitivity
NCT02613117
A Study to Evaluate Oral Malodor and Other Outcomes Following The Use of Two-Step Toothpaste Oral Hygiene
NCT02613130
A Pilot Study to Evaluate a Molecular Method for Plaque
NCT02574221
A Clinical Study to Determine the Safety and Effectiveness of Dentinal Hypersensitivity Treatment With Two Different Toothbrushes
NCT02513212
A Pilot Study to Evaluate a Method for Plaque When Comparing Stannous Fluoride Toothpaste to a Regular Dentifrice
NCT02543060
Effects of an Oxalate Containing Product on Dentinal Hypersensitivity With Dental Prophylaxis
NCT02481557
A Pilot Study to Assess Nominal Versus Controlled Stimuli on Dentinal Hypersensitivity
NCT02406573
A Pilot Clinical Study to Evaluate the Safety and Efficacy of Marketed Oxalate Strips Compared to a Marketed Safety Pen
NCT02384044
A Study to Evaluate the Safety and Efficacy of an Oxalate Strip on Adjacent Teeth With Dentinal Hypersensitivity
NCT02293044
A Clinical Study of Two Dentinal Hypersensitivity Treatments Used With Normal Oral Hygiene
NCT02221349
Effectiveness of Two Water-Based Potassium Oxalate Desensitizers
NCT02192307
Evaluation of the Safety and Efficacy of an Oxalate Gel or Negative Control on Dentinal Hypersensitivity
NCT02189382
A Clinical Study to Assess the Safety of a Disposable Intra-vaginal Device for Stress Urinary Incontinence
NCT02160314
A Clinical Study of the Effectiveness and Safety of a Disposable Intra-vaginal Device for Stress Urinary Incontinence (SUI)
NCT02131311
Effectiveness of Two Water-Based Potassium Oxalate Desensitizers on Dental Hypersensitivity
NCT02152826
Study of Psyllium 6.8 g Versus Placebo on Satiety in Healthy Volunteers
NCT01809925
A Pilot Clinical Study of the Efficacy and Safety of a Disposable Intravaginal Device for Stress Urinary Incontinence
NCT01762345
Comparison of Psyllium and Microcrystalline Cellulose on Glycemic Measures in Subjects With Impaired Fasting Glucose
NCT01549600
Oral Hygiene and Maternity Outcomes Multicenter Study (OHMOM)
NCT01549587
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 7 |
| Phase 2 | 4 |
| Phase 3 | 3 |
| Phase 4 | 9 |
Therapeutic Areas
What the Pipeline for Procter and Gamble Shows
According to the ClinicalTrials.gov registry, Procter and Gamble is linked to 70 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 65 are already marked complete, representing roughly 93% of the total.
The phase mix for Procter and Gamble reports 12 late-stage studies (Phase 3 and Phase 4 combined) and 11 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Procter and Gamble is Gingivitis with 5 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.