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Haleon Clinical Studies

Trusted Science

Welcome to the Haleon Clinical Studies Portal. Here you will find our study register, a portal to request data from our studies, as well as a link to our legacy studies while we were GSK Consumer Healthcare and part of the GSK group of companies.

Haleon understands the importance of transparency and publicly discloses information from the sponsored studies that evaluate our products, irrespective of whether the results are likely to be perceived as positive or negative. Please find our full position on Clinical Research Transparency. To see our approach to clinical trials, click here.

The Haleon Study Register below provides key information about our sponsored studies and supplements information presented in scientific journals, at scientific congresses, in letters to healthcare professionals, and in approved product labels.

Data Sharing Requests

Haleon is committed to sharing data from our clinical studies based on an evaluation of the request. Click here if you'd like to make a request.
Legacy Study Information

For studies on our products conducted prior to February 2022, while we were GSK Consumer Healthcare and part of the GSK group of companies, please search the GSK register: http://www.gsk-studyregister.com. You can submit data sharing request on those studies here.

Haleon Studies

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Sponsor	Therapy Area	Condition	Product	Study ID	Study Title	Study Dates	Protocol Information	Results Summaries
Oral Health\|Dentin Sensitivity\|Toothpaste\|Stannous Fluoride\|300026\|A 12-Week, Randomised, Controlled, Examiner-blind, Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste for the Relief of Dentine Hypersensitivity in a Chinese Population\|8 May 2023\|19 Sep 2023\|https://www.clinicaltrials.gov/study/NCT05750745?term=300026&checkSpell=false&rank=1\|300026_Protocol Summary\|\|\|\|300026_Full Protocol and Statistical Analysis Plan.pdf\|\|\|\|https://clinicaltrials.gov/study/NCT05750745?term=300026&rank=1&tab=results\|300026_Results Summary\|\|\|\|\|\|../DownloadPostingFile.ashx?PostingID=44&FileID=226eaec5-2970-ef11-a8f9-6045bda1a577\|\|../DownloadPostingFile.ashx?PostingID=44&FileID=224dee6b-2970-ef11-a8f9-6045bda1a577\|\|	Oral Health	Dentin Sensitivity	Product Name Stannous Fluoride Product Type Toothpaste	300026	A 12-Week, Randomised, Controlled, Examiner-blind, Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste for the Relief of Dentine Hypersensitivity in a Chinese Population	Start Date 8 May 2023 End Date 19 Sep 2023	300026_Protocol Summary 300026_Full Protocol and Statistical Analysis Plan.pdf	300026_Results Summary
Oral Health\|Gingivitis\|Toothpaste\|Stannous Fluoride\|300211\|A 12-Week, Randomised, Controlled, Examiner-blind, Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste With a Cetylpyridinium Chloride Mouthwash in Improving Gingival Health and Reducing Plaque Accumulation\|11 Nov 2024\|\|https://clinicaltrials.gov/study/NCT06660069?term=Haleon&viewType=Table&rank=1\|300211_Protocol Summary\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|	Oral Health	Gingivitis	Product Name Stannous Fluoride Product Type Toothpaste	300211	A 12-Week, Randomised, Controlled, Examiner-blind, Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Toothpaste With a Cetylpyridinium Chloride Mouthwash in Improving Gingival Health and Reducing Plaque Accumulation	Start Date 11 Nov 2024 End Date	300211_Protocol Summary
Oral Health\|Gingivitis\|Toothpaste\|Stannous Fluoride + Zinc Chloride\|300178\|A 4-Week Randomised, Controlled, Examiner-blind, Clinical Study Investigating the Efficacy of an Experimental Toothpaste Containing Stannous Fluoride in Improving Gingival Health\|23 Sep 2024\|\|https://clinicaltrials.gov/study/NCT06602466?term=300178&rank=1\|300178_Protocol Summary\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|	Oral Health	Gingivitis	Product Name Stannous Fluoride + Zinc Chloride Product Type Toothpaste	300178	A 4-Week Randomised, Controlled, Examiner-blind, Clinical Study Investigating the Efficacy of an Experimental Toothpaste Containing Stannous Fluoride in Improving Gingival Health	Start Date 23 Sep 2024 End Date	300178_Protocol Summary
Skin Care\|Sunscreening Agents\|Lip Care\|Sunscreen Lip Balm\|218004\|A Clinical Study to Evaluate the 8-Hour Moisturization Efficacy of an Over-The-Counter (OTC) Sunscreen Lip Balm After a Single Application\|1 Nov 2021\|11 Nov 2021\|https://clinicaltrials.gov/ct2/show/NCT05082376?term=218004&draw=2&rank=1\|218004_Protocol Summary\|\|\|\|\|\|\|218004_Full Protocol.pdf\|https://clinicaltrials.gov/study/NCT05082376?term=218004&rank=1&tab=results\|218004_Results Summary\|\|\|\|\|\|\|../DownloadPostingFile.ashx?PostingID=36&FileID=16266dc3-b7ba-ed11-a8eb-6045bda1a577\|../DownloadPostingFile.ashx?PostingID=36&FileID=aac52eda-79e3-ed11-a8ee-6045bda1a577\|\|	Skin Care	Sunscreening Agents	Product Name Sunscreen Lip Balm Product Type Lip Care	218004	A Clinical Study to Evaluate the 8-Hour Moisturization Efficacy of an Over-The-Counter (OTC) Sunscreen Lip Balm After a Single Application	Start Date 1 Nov 2021 End Date 11 Nov 2021	218004_Protocol Summary 218004_Full Protocol.pdf	218004_Results Summary
Skin Care\|Sunscreening Agents\|Lip Care\|Sunscreen Lip Balm\|218006\|A Clinical Study to Evaluate the 8-Hour Moisturization Efficacy of an Over-The-Counter Sunscreen Lip Balm After a Single Application\|7 Dec 2021\|17 Dec 2021\|https://clinicaltrials.gov/ct2/show/NCT05109117?term=218006&draw=2&rank=1\|218006_Protocol Summary\|\|\|\|\|\|\|218006_Full Protocol.pdf\|https://clinicaltrials.gov/study/NCT05109117?term=218006&rank=1&tab=results\|218006_Results Summary\|\|\|\|\|\|\|../DownloadPostingFile.ashx?PostingID=35&FileID=4c7d1d78-b7ba-ed11-a8eb-6045bda1a577\|../DownloadPostingFile.ashx?PostingID=35&FileID=00551a50-78e3-ed11-a8ee-6045bda1a577\|\|	Skin Care	Sunscreening Agents	Product Name Sunscreen Lip Balm Product Type Lip Care	218006	A Clinical Study to Evaluate the 8-Hour Moisturization Efficacy of an Over-The-Counter Sunscreen Lip Balm After a Single Application	Start Date 7 Dec 2021 End Date 17 Dec 2021	218006_Protocol Summary 218006_Full Protocol.pdf	218006_Results Summary
Pain Relief\|Pain\|Pain Reliever\|Paracetamol\|300141\|A Phase I, Randomised, Open Label, Single Center, Single Oral Dose, Three Treatment, Three Period, Three Sequence, Change-over Bioequivalence Study of Paracetamol Orodispersible Tablet 500 mg (Haleon) to Assess Bioequivalence With Alvedon 500 mg Film-Coated Tablet (Haleon, Sweden) and Panadol 500 mg Film-Coated Tablet (Haleon, Australia) in Healthy Adult Subjects Under Fasting Conditions\|5 Mar 2025\|\|https://clinicaltrials.gov/study/NCT06855576?term=300141&rank=1\|300141_Protocol Summary\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|	Pain Relief	Pain	Product Name Paracetamol Product Type Pain Reliever	300141	A Phase I, Randomised, Open Label, Single Center, Single Oral Dose, Three Treatment, Three Period, Three Sequence, Change-over Bioequivalence Study of Paracetamol Orodispersible Tablet 500 mg (Haleon) to Assess Bioequivalence With Alvedon 500 mg Film-Coated Tablet (Haleon, Sweden) and Panadol 500 mg Film-Coated Tablet (Haleon, Australia) in Healthy Adult Subjects Under Fasting Conditions	Start Date 5 Mar 2025 End Date	300141_Protocol Summary
Pain Relief\|Pain\|Pain Reliever\|Diclofenac diethylamine\|300099\|A Post-hoc Analysis of Data Obtained from China 1.16% and 2.32% Study to Evaluate Relationship Between Treatment Compliance and Pain Relief in Ankle Sprain Patients\|26 Apr 2023\|10 Aug 2023\|\|\|300099_Protocol Summary.pdf\|\|\|300099_Statistical Analysis Plan.pdf\|\|\|\|\|\|300099_Results Summary.pdf\|\|\|\|../DownloadPostingFile.ashx?PostingID=57&FileID=a10317ba-b574-ef11-a8f9-6045bda1a577\|../DownloadPostingFile.ashx?PostingID=57&FileID=2abd3c1d-cc91-ef11-a8f9-6045bda1a577\|\|../DownloadPostingFile.ashx?PostingID=57&FileID=6f60bd15-cc91-ef11-a8f9-6045bda1a577\|../DownloadPostingFile.ashx?PostingID=57&FileID=2abd3c1d-cc91-ef11-a8f9-6045bda1a577\|	Pain Relief	Pain	Product Name Diclofenac diethylamine Product Type Pain Reliever	300099	A Post-hoc Analysis of Data Obtained from China 1.16% and 2.32% Study to Evaluate Relationship Between Treatment Compliance and Pain Relief in Ankle Sprain Patients	Start Date 26 Apr 2023 End Date 10 Aug 2023	300099_Protocol Summary.pdf 300099_Statistical Analysis Plan.pdf	300099_Results Summary.pdf
Pain Relief\|Pain\|Pain Reliever\|Diclofenac diethylamine\|300098\|A Post-hoc Analysis of Study Data Obtained From China 1.16% And 2.32% Study To Evaluate ‘Time To Onset Of Pain Relief’ In Ankle Sprain Patients\|28 Apr 2023\|25 Jun 2023\|\|\|300098_Protocol Summary.pdf\|\|\|300098_Statistical Analysis Plan.pdf\|\|\|\|\|\|300098_Results Summary.pdf\|\|\|\|../DownloadPostingFile.ashx?PostingID=48&FileID=fb33d3c1-3ab4-ee11-a8f4-6045bda1a577\|../DownloadPostingFile.ashx?PostingID=48&FileID=68c22c90-2323-ef11-a8f7-6045bda1a577\|\|../DownloadPostingFile.ashx?PostingID=48&FileID=8960e20c-2423-ef11-a8f7-6045bda1a577\|\|	Pain Relief	Pain	Product Name Diclofenac diethylamine Product Type Pain Reliever	300098	A Post-hoc Analysis of Study Data Obtained From China 1.16% And 2.32% Study To Evaluate ‘Time To Onset Of Pain Relief’ In Ankle Sprain Patients	Start Date 28 Apr 2023 End Date 25 Jun 2023	300098_Protocol Summary.pdf 300098_Statistical Analysis Plan.pdf	300098_Results Summary.pdf
Oral Health\|Denture Retention\|Denture Adhesive\|Poly (methylvinylether/Maleic Acid) Sodium-Calcium Mixed Partial Salt + Sodium Carboxymethylcellulose\|213380\|A Post-hoc Pooled Analysis of GSK CH Clinical Data Investigating the Efficacy of Denture Adhesive creams containing PMV/MA &CMC on Denture Retention and Bite Force\|17 Dec 2020\|19 May 2021\|https://www.gsk-studyregister.com/en/trial-details/?id=213380\|213380_Protocol Summary\|\|\|\|\|\|\|213380_Protocol and Statistical Analysis Plan.pdf\|\|\|213380_Result Summary.pdf\|\|\|\|\|\|../DownloadPostingFile.ashx?PostingID=25&FileID=690a9b50-1ebc-ed11-a8eb-6045bda1a577\|../DownloadPostingFile.ashx?PostingID=25&FileID=6a0a9b50-1ebc-ed11-a8eb-6045bda1a577\|\|	Oral Health	Denture Retention	Product Name Poly (methylvinylether/Maleic Acid) Sodium-Calcium Mixed Partial Salt + Sodium Carboxymethylcellulose Product Type Denture Adhesive	213380	A Post-hoc Pooled Analysis of GSK CH Clinical Data Investigating the Efficacy of Denture Adhesive creams containing PMV/MA &CMC on Denture Retention and Bite Force	Start Date 17 Dec 2020 End Date 19 May 2021	213380_Protocol Summary 213380_Protocol and Statistical Analysis Plan.pdf	213380_Result Summary.pdf
Pain Relief\|Pain\|Pain Reliever\|Diclofenac diethylamine\|300128\|A Prospective Real-World Evidence Study Evaluating the Effects of Voltaren Use on Mobility and Quality of Life in Participants With Knee Osteoarthritis (OA) Pain \|19 Apr 2024\|\|https://www.clinicaltrials.gov/study/NCT06379893?term=300128&rank=1\|300128_Protocol Summary \|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|\|	Pain Relief	Pain	Product Name Diclofenac diethylamine Product Type Pain Reliever	300128	A Prospective Real-World Evidence Study Evaluating the Effects of Voltaren Use on Mobility and Quality of Life in Participants With Knee Osteoarthritis (OA) Pain	Start Date 19 Apr 2024 End Date	300128_Protocol Summary

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*For studies on our products conducted prior to February 2022, while we were GSK Consumer Healthcare and part of the GSK group of companies, please search the GSK register: http://www.gsk-studyregister.com.

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