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Organization (Industry)

PROCTER & GAMBLE Co

ClinicalTrials.gov lists PROCTER & GAMBLE Co as lead sponsor of 83 trials. It has 11 active development programs and 17 approved assets.

US Industry Manufacturer CIK 0000080424
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14 0 1993 2026

Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.

2026 is partial: 1 registered with a 2026 start date. The dashed outline is the pace from the 0 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 2.8 trial starts a year over the five years to September, under the 5 a year the method needs.

Logo Procter & Gamble. The original uploader was KarimKoueider at English Wikipedia .. Later version(s) were uploaded by Cristianocampo93 , JJMC89 , Ridwan97 at en.wikipedia ., via Wikimedia Commons, Public domain. Shown to identify the organization; it may be a registered trademark.

This page covers PROCTER & GAMBLE Co: 83 lead-sponsored trials and 13 legal-entity registrations.

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Disease areas (71)

Shown in this order: most trials first.

Disease areas
Disease area Trials
Gingivitis 22
Bone Diseases, Metabolic 19
Osteoporosis 19
Dentin Sensitivity 11
Osteoporosis, Postmenopausal 8

Trials by start year as sponsor or collaborator (28)

Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Show the table of trials by start year as sponsor or collaborator
Trials by start year as sponsor or collaborator
Year Trials started
2026 (partial year) 1
2025 4
2023 3
2022 5
2021 6
2020 4
2019 4
2018 14
2017 4
2016 3

Recruitment duration, a model prediction: 2 trials still running at the 2026-10-09 snapshot, fewer than the 5 needed for a median. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

Active development programs (11)

Shown in this order: max phase, then active trials.

Active development programs
Drug Disease area Max phase Trials
0.76% Sodium Monofluorophosphate Dentifrice Gingivitis Phase 1 3
0.454% Stannous Fluoride Dentifrice Gingivitis Phase 1 3
0.454% stannous fluoride Gingivitis Not reported 3
0.76% sodium monofluorophosphate Gingivitis Not reported 2
0.454% stannous fluoride AM and 0.76% sodium monofluorophosphate PM Gingivitis Not reported 2

Approved assets (17)

Shown in this order: max phase first.

Approved assets
Drug Trials
Stannous Fluoride Dentifrice 7
Sodium monofluorophosphate dentifrice 2
0 ppm F 2
Marketed Toothpaste 2
1100 ppm as MFP 2

Sponsor delivery record (1)

Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.

Sponsor delivery record
Enrollment Timeline
71% hit target (n=7) 67% on time (n=9)

Journals published in (64)

Shown in this order: most published in first.

Journals published in
Journal Publications
American heart journal 6
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 6
The Cochrane database of systematic reviews 4
The American journal of gastroenterology 3
The Journal of clinical endocrinology and metabolism 3

US granted patents (1)

Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.

US granted patents
US patents granted Granted in the last 5 years Most recent grant
17,267 2,025 2025-12-30

SEC-reported annual financials (12)

Shown in this order: newest fiscal year first; SEC EDGAR XBRL companyfacts, USD as reported.

SEC-reported annual financials
Fiscal year Revenue (USD) Net income (USD) R&D (USD)
2026 87,032,000,000 16,046,000,000 2,100,000,000
2025 84,284,000,000 15,974,000,000 2,100,000,000
2024 84,039,000,000 14,879,000,000 2,000,000,000
2023 82,006,000,000 14,653,000,000 2,000,000,000
2022 80,187,000,000 14,742,000,000 2,000,000,000
2021 76,118,000,000 14,306,000,000 1,900,000,000
2020 70,950,000,000 13,027,000,000 1,800,000,000
2019 67,684,000,000 3,897,000,000 1,900,000,000
2018 66,832,000,000 9,750,000,000 1,900,000,000
2017 65,058,000,000 15,326,000,000 1,900,000,000

Financing and grant events (70)

Shown in this order: most recent first.

Financing and grant events
Date Round type Amount (USD) Source
2025-11-04 Debt financing 258,889,000 Sec extracted
2025-11-03 Debt financing 1,250,000,000 Sec extracted
2025-10-30 Debt financing 258,889,000 Edgar offerings
2025-10-29 Debt financing 1,160,722,401 Edgar offerings
2025-10-29 Debt financing 1,248,525,000 Edgar offerings

FDA inspection record (1)

FDA inspection record
Latest classification Inspections
VAI 10

FDA recalls (3)

Shown in this order: most recent first.

FDA recalls
Product Classification Initiated
Vicks NyQuil Cold and Flu Nighttime Relief, Liquid Twin Pack, (Acetaminophen 650mg, Dextromethorphan HBr 30mg, Doxylamine succinate 12.5mg), 12 fl oz (354 ml) bottles, Distributed by Procter & Gamble, Cincinnati, OH 45202, NDC 37000-807-12 Class II 2013-08-29
DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine HCl 5 mg) liquicaps and NyQuil Sinex NightTime Sinus Relief (acetaminophen 325 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg) liquicaps Combopack, each 48-count liquicaps per carton contains 32 DayQuil Sinex DayTime Liquicaps and 16 NyQuil Sinex NightTime Liquicaps per carton, Made In Canada, Dist. by Procter & Gamble, Cincinnati, OH 45202, UPC 3 23900 01454 1. Class II 2013-07-03
Vicks NyQuil Cold & Flu, Nighttime Relief, 12 FL OZ bottle, Dist. by Proctor and Gamble, Cincinnati, OH 45040. NDC 37000-808-12 Class II 2012-11-08

FDA import refusals (1)

FDA import refusals
Refused import lines Latest refusal
47 2026-05-19

Manufacturing and distribution sites (1)

Manufacturing and distribution sites
Facility Location Regulators Member organization
PROCTER & GAMBLE CO. CINCINNATI, US FDA

Climate targets, as filed (1)

Climate targets, as filed
Reporting year Net-zero target
2025 2040

Workforce and board diversity, as filed (1)

Workforce and board diversity, as filed
Reporting year Workforce % women Board % women
2025 42.0% not disclosed

Organization relationships (13)

Shown in this order: most evidence first.

Organization relationships
Related organization Relationship Evidence
Vanderbilt University Co sponsors trial with 2
University of Chicago Co sponsors trial with 1
Government of the United States of America Co sponsors trial with 1
Autonomous University of Queretaro Co sponsors trial with 1
University of Washington Co sponsors trial with 1

Latest dated events (17,553)

Shown in this order: newest first.

Latest dated events
Date Event Source
2026-10-28 Trial started Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI))
2026-05-19 FDA import refusal FDA enforcement (warning and untitled letters, recalls, inspections, import refusals, debarment)
2025-12-30 Patent granted Granted US patents (PatentsView / USPTO)
2025-12-30 Patent granted Granted US patents (PatentsView / USPTO)
2025-12-30 Patent granted Granted US patents (PatentsView / USPTO)

CLIA clinical laboratory certificates (7)

Shown in this order: active first, then certificate type.

CLIA clinical laboratory certificates
Lab Certificate Status
PROCTER & GAMBLE Certificate of waiver Active
PROCTER & GAMBLE (WINTON HILL) Certificate of waiver Active
PROCTER & GAMBLE (F&HC) Certificate of waiver Active
PROCTER & GAMBLE Certificate of waiver Active
PROCTER AND GAMBLE Certificate of waiver Active

Biomarker capability evidence (60)

Shown in this order: tier desc, then gene symbol.

Biomarker capability evidence
Gene Role Evidence
CDA Trial sponsor Named in trial inclusion criteria
CDA Trial sponsor Named in trial inclusion criteria
CYP19A1 Trial collaborator Named in trial inclusion criteria
NF2 Trial collaborator Primary endpoint in a Phase 3 trial
PAPOLA Trial sponsor Named in trial inclusion criteria

Not on this page

Checked, with nothing recorded for this organization: companies grouped under this page, related companies not grouped here, fda warning letters, fda untitled letters, and biomarkers this organization publishes on.