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Compound · clinical trials

Abrysvo clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our Australia, USA, France, Canada and Japan registers that name Abrysvo as an intervention. Synced 26 Sep 2026
6Current trials
2Recruiting now
4Lead sponsors
5Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Abrysvo is named as an intervention in 6 current clinical trials in our Australia, USA, France, Canada and Japan registers. 2 are recruiting patients now. The most common phase is Observational. The sponsor with the most trials is Pfizer (3). The most-studied condition is Respiratory Syncytial Virus (RSV).

Trials by status

  • Recruiting233%
  • Not yet open117%
  • Active, closed350%

Trials by phase

  • Observational350%
  • Phase 3117%
  • Phase 4117%
  • Phase 1117%
01

Clinical trials of Abrysvo

6 trials
StudyPhaseStatusLead sponsorRegisters
Concurrent Versus Sequential Administration of Tdap and RSV Vaccines in Pregnancy
NCT07097012 · ClinicalTrials.gov ↗ · RSV, Tdap - Tetanus, Diphtheria and Acellular Pertussis Vaccination, Pregnancy
Phase 4 Recruiting Canadian Immunization Research Network Canada
Prevention of RSV Infection in Infants by Administering Nirsevimab to Infants, With or Without Maternal RSV Vaccination
NCT07232706 · ClinicalTrials.gov ↗ · RSV Immunization
Phase 3 Recruiting Centre Hospitalier Annecy Genevois France
Safety, Tolerability and Immunogenicity of a Maternal Respiratory Syncytial Virus (RSV) Vaccine (MKK900) in Healthy Adult Women
NCT07492706 · ClinicalTrials.gov ↗ · Respiratory Syncytial Virus (RSV)
Phase 1 Not yet open MAXVAX Biotechnology Limited Liability Company Australia
SPECIAL INVESTIGATION FOR ABRYSVO IN INDIVIDUALS AGED 60 YEARS OR OLDER
NCT06546800 · ClinicalTrials.gov ↗ · Respiratory Syncytial Virus Infection
Observational Active, closed Pfizer Japan
STudy of Real World vaccinE Effectiveness of maTernal RSVpreF vaccinatiON Against Respiratory Syncytial Virus (RSV) in Hospitalised Infants in Australia (STREETON)
NCT07122661 · ClinicalTrials.gov ↗ · Respiratory Syncytial Virus (RSV), Respiratory Syncytial Virus, Lower Respiratory Tract Disease
Observational Active, closed Pfizer Australia
Evaluating ABRYSVO Maternal Vaccine Effectiveness Among Infants
NCT07249320 · ClinicalTrials.gov ↗ · Respiratory Syncytial Virus (RSV)
Observational Active, closed Pfizer USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Abrysvo

10 conditions
Respiratory Syncytial Virus (RSV)3RSV Immunization1RSV1Tdap - Tetanus, Diphtheria and Acellular Pertussis Vaccination1Pregnancy1Healthy1Respiratory Syncytial Virus Infection1Respiratory Syncytial Virus1Lower Respiratory Tract Disease1Respiratory Tract Diseases1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Pfizer3
Centre Hospitalier Annecy Genevois1
Canadian Immunization Research Network1
MAXVAX Biotechnology Limited Liability Company1
04

By country register

RegisterTrialsRecruiting
Clinical trials in Australia20
Clinical trials in USA10
Clinical trials in France11
Clinical trials in Canada11
Clinical trials in Japan10

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

05

Related compounds

06

Questions about Abrysvo trials

How many clinical trials are testing Abrysvo?

6 current trials in our Australia, USA, France, Canada and Japan registers name Abrysvo as a drug or biological intervention, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Abrysvo trials recruiting patients?

Yes. 2 of the 6 trials are recruiting: 1 with sites in France and 1 with sites in Canada. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Abrysvo clinical trials?

Pfizer (3), Centre Hospitalier Annecy Genevois (1), Canadian Immunization Research Network (1) and MAXVAX Biotechnology Limited Liability Company (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Abrysvo works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Abrysvo works or whether it is effective. 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 country trial registers, collects every trial that lists Abrysvo (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. 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 ClinicalTrials.gov 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 โ€” 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 โ€” we correct promptly and log it.