Tobevibart clinical trials
Tobevibart is named as an intervention in 5 current clinical trials in our UK, Germany, France, Spain, Italy, Netherlands, Canada, Austria, Belgium and USA registers. 1 is recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Vir Biotechnology, Inc (4). The most-studied condition is Viral Hepatitis.
Where Tobevibart is approved
All regulators →- 1 EU orphan designation, most recently for treatment of hepatitis delta virus infection (13 Dec 2024, positive)
From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.
How Tobevibart works
All drug targets →- Hepatitis D virus infectionPhase 3
- Chronic hepatitis B virus infectionPhase 2
- Hepatitis B virus infectionPhase 2
Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5314621, CC BY-SA 3.0. The Guide to Pharmacology has no record of this medicine, so its targets rest on ChEMBL alone. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.
Patient leaflets for Tobevibart
The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.
- UKUnited Kingdom: Search MHRA ProductsPatient information leaflets and SmPCs for UK-licensed products.
- USUnited States: Search DailyMedFDA-approved labels, including patient and medication guides.
Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.
Trials by status
Trials by phase
Clinical trials of Tobevibart
5 trialsRegisters 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.
Conditions studied with Tobevibart
3 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| Vir Biotechnology, Inc | 4 |
| University Health Network, Toronto | 1 |
By country register
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about Tobevibart trials
How many clinical trials are testing Tobevibart?
5 current trials in our UK, Germany, France, Spain, Italy, Netherlands, Canada, Austria, Belgium and USA registers name Tobevibart (also registered as VIR-3434) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.
Are Tobevibart trials recruiting patients?
Yes. 1 of the 5 trials is recruiting: 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 Tobevibart clinical trials?
Vir Biotechnology, Inc (4) and University Health Network, Toronto (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 Tobevibart works or whether it is effective, and it is not medical advice.
How this page is built
Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Tobevibart works or whether it is effective. Each trial links to its own record so you can check it yourself.
- ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Tobevibart (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 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.