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NCT Number: NCT07656493

Liposomal Amphotericin B for Invasive Fungal Disease in Solid Organ Transplant Recipients

This real-world observational study aims to evaluate the effectiveness, safety, and therapeutic drug monitoring (TDM) of liposomal amphotericin B (L-AmB) in solid organ transplant recipients with invasive fungal disease (IFD). IFD is a major cause of morbidity and mortality in transplant recipients because of long-term immunosuppressive therapy and increased susceptibility to opportunistic fungal infections.

This is a single-center ambispective cohort study conducted at Sichuan Provincial People's Hospital. The study includes a prospective cohort of solid organ transplant recipients receiving L-AmB therapy and a historical control cohort treated with alternative systemic antifungal regimens. Clinical management and treatment decisions will be determined by treating physicians according to routine clinical practice, and no study-specific intervention will be introduced.

The study will collect information on demographic characteristics, transplant type, immunosuppressive regimens, fungal pathogens, infection sites, antifungal treatment strategies, laboratory findings, and clinical outcomes. Particular attention will be given to renal safety, electrolyte abnormalities, and therapeutic drug monitoring of liposomal amphotericin B. Plasma concentrations of L-AmB, treatment modifications, temporary treatment discontinuation, and concentration-related safety and effectiveness outcomes will be recorded during antifungal therapy.

The primary outcomes are the 28-day clinical response rate and 84-day all-cause mortality. Secondary outcomes include mycological clearance, acute kidney injury, electrolyte abnormalities, breakthrough fungal infection, treatment discontinuation due to adverse events, liposomal amphotericin B plasma concentrations, and the associations between L-AmB exposure and clinical outcomes or treatment-related toxicities.

The study is expected to provide real-world evidence regarding the effectiveness, safety, and pharmacokinetic characteristics of L-AmB in transplant recipients, support optimization of antifungal treatment strategies, and inform individualized dosing and monitoring approaches in this high-risk population.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital

Chengdu, Sichuan, 610072, China

Location contact

Lingai Pan, MD

CONTACT

[email protected]

+86 17708130236

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Liposomal Amphotericin B

Drug

Liposomal amphotericin B administered for treatment of proven, probable, or possible invasive fungal disease in solid organ transplant recipients according to routine clinical practice. Dose adjustment and treatment duration are determined by treating physicians.

Other names: L-AmB

Alternative Systemic Antifungal Therapy

Drug

Alternative systemic antifungal agents including azoles, echinocandins, or other standard antifungal therapies administered according to routine clinical practice in historical control patients with invasive fungal disease.

Other names: Azoles, Echinocandins

Primary outcomes

  1. 28-Day Clinical Response Rate

    Time frame: Day 28

    Proportion of participants achieving complete or partial clinical response at Day 28 after initiation of antifungal therapy.

  2. 84-Day All-Cause Mortality

    Time frame: Day 84

    All-cause mortality occurring within 84 days after initiation of antifungal therapy.

Secondary outcomes

  1. Mycological Clearance Rate

    Time frame: Day 28

    Proportion of participants with documented clearance of fungal pathogens.

  2. Acute Kidney Injury

    Time frame: Baseline through Day 84

    Occurrence of acute kidney injury during antifungal treatment.

  3. Electrolyte Abnormalities

    Time frame: Baseline through Day 84

    Occurrence of hypokalemia, hypomagnesemia, or other treatment-related electrolyte disturbances.

  4. Liposomal Amphotericin B Plasma Concentration

    Time frame: Baseline through Day 84

    Plasma concentration of liposomal amphotericin B measured during antifungal therapy.

  5. Association Between Liposomal Amphotericin B Exposure and Clinical Response

    Time frame: Baseline through Day 84

    Relationship between liposomal amphotericin B plasma concentration and clinical response.

  6. Association Between Liposomal Amphotericin B Exposure and Adverse Events

    Time frame: Baseline through Day 84

    Relationship between liposomal amphotericin B plasma concentration and treatment-related adverse events, including nephrotoxicity and electrolyte abnormalities.

  7. Breakthrough Fungal Infection

    Time frame: Baseline through Day 84

    Occurrence of breakthrough invasive fungal infection during antifungal therapy.

  8. Antifungal Treatment Discontinuation Due to Adverse Events

    Time frame: Baseline through Day 84

    Permanent discontinuation of antifungal therapy because of treatment-related adverse events.

Study contacts

Contact information is provided by the study sponsor or research team.

Lingai Pan, MD

CONTACT

[email protected]

+86 17708130236

Sponsors and collaborators

Lead sponsor

Sichuan Provincial People's Hospital

Other

Collaborators

  • Beijing Science and Technology Innovation Medical Development Foundation

Registry information

Official study title

A Real-World Observational Study of the Effectiveness, Safety, and Therapeutic Drug Monitoring of Liposomal Amphotericin B in Solid Organ Transplant Recipients With Invasive Fungal Disease

Acronym: LAMB-SOT

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jun 18, 2026
Registry last updated
Jun 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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