Welcome to GSK clinical study register

We invite you to explore our study register to learn more about our clinical trials and how they help advance medicines and vaccines.

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Clinical trials are a collaborative effort. We work alongside healthcare professionals, researchers, and volunteers around the globe to explore innovative medicines and vaccines. Every participant and clinical trial brings us one step closer to breakthroughs that can transform lives.

About GSK study register

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The GSK study register provides information on existing vaccines and medicines clinical trials such as the purpose, design, locations and eligibility criteria for participating, in addition to links to clinical trial documents that are currently available. Please see other public registries (e.g. ClinicalTrials.gov) for any trial disclosures from our alliance partners.

GSK’s long-standing commitment to clinical trial transparency

We recognize the importance of publicly disclosing clinical research on our products. In 2004 we introduced the GSK study register, a place where anyone can access information about the clinical research we carry out. We were the first pharmaceutical company to do this.​

Our clinical trial results are made public regardless of whether they are positive or negative. Before the trial begins, we publicly register the study protocol summary, which includes the trial’s objectives and design. Once the clinical trial has completed, we disclose a summary of the results, a plain language summary of results (for Phase 2-4 clinical trials only), redacted* version of the full study protocol, the statistical analysis plan and clinical trial report synopsis. We also list the clinical trials that are available for patient-level data sharing. Click here to find more information about our commitments.​

We disclose all studies that evaluate the clinical efficacy and/or safety or effectiveness of our medicines and vaccines. As part of our commitment to transparency of clinical research responsible business performance report 2024, we have made over 7,400 protocol summaries and over 6,500 results summaries available since the GSK study register was set up in 2004.

* Personal information and commercially confidential information

Number of Protocol Summaries Registered
1

Number of protocol summaries registered

Number of Results Summaries Disclosed
2

Number of results summaries disclosed

Updated as of 15 January 2025

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Plain language summaries

GSK is committed to developing plain language summaries, or layperson summaries of Phase 2-4 clinical trials results, in a way that is understandable by the general public.

Sharing these summaries is a crucial part of showing respect to volunteers who participated in our clinical trials and our commitment to providing access to information about our research and their results to participants, healthcare providers and the wider public.

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Sharing clinical trial data

GSK is committed to provide access to anonymized participant-level data that sit behind the results of clinical trials. GSK-sponsored interventional clinical trials conducted with products will be listed for data sharing once a medicine or a vaccine has been approved by regulators or terminated from development, and the trial has fulfilled its publication requirements.

External researchers can request access to anonymized participant-level clinical trial data and supporting clinical trial documents through the multi-sponsor data sharing portals. Qualified researchers can request access to our studies by providing a research proposal with a comitment to publish their findings. It is hoped that sharing these data with researchers will help to further scientific research, enhance understanding of new and existing medicines and vaccines, and ultimately improve participant care.