RecruitingNCT07185503

Liposomal Amphotericin B Plus Posaconazole/Isavuconazole for Mucormycosis in Hematologic Malignancies: Efficacy and Safety

The Efficacy and Safety of Liposomal Amphotericin B 3-5mg/kg Combined With Posaconazole/Isavuconazole for the Treatment of Mucormycosis in Patients With Hematologic Malignancies


Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Enrollment

60 participants

Start Date

Mar 25, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

This clinical trial, a single-arm prospective study, aims to evaluate the efficacy and safety of liposomal amphotericin B (3-5 mg/kg/day) combined with posaconazole/isavuconazole in treating adult patients with malignant hematological diseases complicated by mucormycosis. The primary objectives are to determine the proportion of patients achieving complete or partial resolution of mucormycosis symptoms and to identify prognostic factors influencing survival outcomes. Participants will receive the combination therapy, undergo regular monitoring of symptoms, adverse events, and disease progression via radiological and laboratory assessments, and complete follow-up visits to track long-term survival. The study will analyze composite response rates, treatment-related adverse events, and survival data to refine therapeutic strategies for this high-risk population.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called liposomal amphotericin B (3-5 mg/kg/day) combined with posaconazole/isavuconazole for people with mucormycosis in hematologic malignancies. The study is currently recruiting participants at 9 locations. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGliposomal amphotericin B (3-5 mg/kg/day) combined with posaconazole/isavuconazole

The intervention in this study is a tailored antifungal regimen combining liposomal amphotericin B (L-AmB) (3-5 mg/kg/day IV) with posaconazole or isavuconazole (300 mg/200 mg daily, oral or IV), designed to optimize efficacy and safety in immunocompromised adults with blood cancers and mucormycosis. Dosing and duration are personalized based on clinical response, immune recovery, and organ function, with a focus on transitioning to oral therapy to reduce hospitalization. The study emphasizes rigorous safety monitoring, prohibited unauthorized antifungal co-medications, and explores prognostic factors to advance treatment strategies for this high-risk population.


Locations(9)

The Second Hospital of Dalian Medical University

Dalian, China

The First Affiliated Hospital of Harbin Medical University

Harbin, China

Shengjing Hospital of China Medical University

Shenyang, China

The First Affiliated Hospital of China Medical University

Shenyang, China

Tianjin First Central Hospital

Tianjin, China

Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College

Tianjin, China

Second Hospital of Tianjin Medical University

Tianjin, China

Tianjin Haihe Hospital

Tianjin, China

Tianjin Union Medical Center of Nankai University

Tianjin, China

View Full Details on ClinicalTrials.gov

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NCT07185503