New study to test antifungal drug safety in organ transplant patients
NCT ID NCT07656493
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will observe 120 solid organ transplant recipients who have invasive fungal infections. Researchers will track how well the drug liposomal amphotericin B works and its side effects, compared to historical patients who received other antifungal treatments. The goal is to gather real-world evidence to guide better dosing and monitoring in this high-risk group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Liposomal amphotericin B (an antifungal drug)
- What this could lead to
- If successful, this study could provide real-world data to help doctors better treat fungal infections in transplant patients, potentially improving survival and reducing side effects.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be influenced by other factors. It is also small (120 participants) and single-center, limiting how widely findings can be applied.
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.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
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.
Who is studied
Adult solid organ transplant recipients diagnosed with proven, probable, or possible invasive fungal disease and treated with liposomal amphotericin B or alternative systemic antifungal therapy at Sichuan Provincial People's Hospital.
- 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: * Age 18 to 75 years. * Recipient of a solid organ transplant. * Diagnosis of invasive fungal disease (IFD) according to EORTC/MSGERC criteria. * Receiving liposomal amphotericin B therapy as part of routine clinical care. * Provision of informed consent for prospective participants. Exclusion Criteria: * Known hypersensitivity to amphotericin B formulations. * Severe hepatic dysfunction (ALT or AST \>5× upper limit of normal, or total bilirubin \>2× upper limit of normal). * Severe renal dysfunction requiring permanent discontinuation of antifungal therapy at baseline. * Pregnancy or breastfeeding. * Participation judged inappropriate by the investigator.
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital
Chengdu, Sichuan, 610072, China
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Other studies related to the condition(s) this trial covers.
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