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GlaxoSmithKline Biologicals clinical trials

Source: the EU Clinical Trials Information System (CTIS) — current trials in our EU (CTIS) register with GlaxoSmithKline Biologicals as lead sponsor. Synced 26 Sep 2026
5Current trials
0Recruiting now
0Drugs in these trials
1Trial register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

GlaxoSmithKline Biologicals is the lead sponsor of 5 current clinical trials in our EU (CTIS) register.

Company profile on this site (news, sites, medicines, approvals): GSK (GB) →
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GlaxoSmithKline Biologicals in the EU trials register (CTIS)

5 trials

Authorised or ongoing trials in the EU Clinical Trials Information System with GlaxoSmithKline Biologicals as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A phase 3 randomized, observer-blind, controlled study to evaluate the immunogenicity, reactogenicity and safety of an mRNA-based seasonal influenza vaccine, in adults 18-64 years of age
2026-526925-17-00 · Virus Diseases
Phase 3 Authorised Belgium, Germany
A phase 3 randomized, observer-blind, controlled study to evaluate the clinical efficacy of an mRNA- based seasonal influenza vaccine in older adults ≥65 years of age
2026-526682-14-00 · Virus Diseases
Phase 3 Authorised Belgium, Germany, Finland
A Phase 3a, observer blind, randomized, controlled study to evaluate the immunogenicity and safety of intramuscular administration of an investigational combined measles, mumps, rubella, and varicella vaccine compared with intramuscular administration of ProQuad when administered as a second dose to healthy children aged 15 months to 6 years of age
2025-523274-17-00 · Virus Diseases
Phase 3 Authorised Spain, Germany
A study on the safety of and immune response to different doses of RSV/hMPV combination and hMPV vaccines in adults
2025-524456-58-00 · CTIS ↗ · Respiratory Tract Diseases
Phase 1 Authorised Belgium
A Phase 2b, non-randomized, controlled, open-label, extension study to evaluate the persistence of immune response of the adjuvanted RSVPreF3 vaccine and the safety and immunogenicity following revaccination in lung and kidney transplant recipients (≥18 years of age)
2024-519730-23-00 · CTIS ↗ · Respiratory Tract Diseases
Phase 2 Ongoing Italy, Germany, Spain
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By trial register

RegisterTrialsRecruiting
EU register (CTIS)5—

A trial with sites in more than one country appears in each of those registers.

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Questions about GlaxoSmithKline Biologicals trials

How many clinical trials does GlaxoSmithKline Biologicals sponsor?

GlaxoSmithKline Biologicals is the lead sponsor of 5 authorised or ongoing trials in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.