Could a common herpes drug ease cancer treatment's painful mouth sores?
NCT ID NCT07363031
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether the antiviral drug valacyclovir can prevent or reduce painful mouth sores (oral mucositis) in adults receiving radiotherapy for head and neck cancer. Researchers will give either valacyclovir or a placebo to 84 participants during their radiation treatment. They will monitor mouth sores, pain, and herpesvirus activity to see if the drug helps.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Valacyclovir
- What this could lead to
- If it works, this could point toward a simple antiviral pill to prevent severe mouth sores during head and neck cancer radiotherapy.
- What could go wrong
- This is a small, early-phase trial. The benefit may be small or absent, and valacyclovir can cause side effects like nausea or headache.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 84 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2022
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 years or older. * Diagnosis of head and neck cancer. * Planned to receive curative or definitive radiotherapy to the head and neck region. * Ability to swallow oral medication. * Adequate clinical condition to participate in study procedures. * Ability to provide written informed consent. Exclusion Criteria: * Known hypersensitivity or contraindication to valacyclovir or related antiviral agents. * Current or recent use of systemic antiviral therapy. * Severe renal impairment requiring dose adjustment or contraindicating valacyclovir use. * Active oral infection requiring systemic antimicrobial treatment at baseline. * Pregnant or breastfeeding individuals. * Participation in another interventional clinical trial that may interfere with study outcomes.
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Instituto Oncoclinicas
Rio de Janeiro, Rio de Janeiro, 22250-905, Brazil
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Other studies related to the condition(s) this trial covers.
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