Liposomal Amphotericin B + Flucytosine for Fungal Infection

(LAmB-FAST Trial)

Not yet recruiting at 10 trial locations
TL
Overseen ByThuy Le, MD, PhD
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: Duke University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to find better ways to treat talaromycosis, a fungal infection, in people with HIV. It will test whether a single dose of liposomal amphotericin B (an antifungal medicine) is more effective than the standard 14-day treatment. The trial will also evaluate if adding flucytosine (another antifungal drug) improves treatment outcomes. Additionally, it will explore whether monitoring HIV levels can guide when to stop itraconazole to prevent the infection's recurrence. People with HIV diagnosed with talaromycosis are suitable candidates for this trial. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking treatment advancements.

Do I need to stop my current medications to join the trial?

The trial information does not specify if you need to stop taking your current medications. However, it does mention that participants should not have received more than 2 doses of conventional amphotericin B, which might imply some restrictions on similar treatments.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that liposomal amphotericin B (LAmB) is generally safe for treating fungal infections. The FDA has approved it for certain infections, indicating it has passed strict safety tests for those uses. Studies suggest that LAmB may be less harmful than an older version, deoxycholate amphotericin B (DAmB). Specifically, LAmB is associated with a 24.8% mortality rate over ten weeks, one of the lowest rates observed in similar research.

Researchers have also studied deoxycholate amphotericin B combined with flucytosine, finding that this combination improves survival rates in fungal infections. However, DAmB can sometimes cause side effects like kidney problems or anemia (a low red blood cell count). Doctors often follow specific procedures to minimize these risks.

Both treatments are used for serious infections, and their safety has been well-documented. For those considering joining a trial, it's important to know that these drugs have been thoroughly studied for safety in humans.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about these treatments because Liposomal Amphotericin B (LAmB) plus Flucytosine (5FC) and Deoxycholate Amphotericin B (DAmB) plus 5FC offer unique approaches to treating fungal infections. Unlike traditional treatments that often require longer durations, LAmB delivers a high dose in a single infusion, potentially reducing treatment time and side effects. Meanwhile, DAmB plus 5FC provides an alternative with a different formulation of Amphotericin B, which might improve patient outcomes by enhancing the effectiveness of the antifungal combination. Both treatments aim to target the fungal infection more effectively, which could lead to quicker recovery and fewer complications for patients.

What evidence suggests that this trial's treatments could be effective for HIV-associated talaromycosis?

Research has shown that a single 10 mg/kg dose of liposomal amphotericin B matches the effectiveness of the traditional 14-day treatment with deoxycholate amphotericin B for fungal infections. This trial evaluates both liposomal and deoxycholate amphotericin B, with some participants receiving flucytosine and others a placebo. Adding flucytosine to amphotericin B can further improve survival rates in patients with severe fungal infections. These treatments have demonstrated good results, especially for widespread fungal infections. Both liposomal and deoxycholate amphotericin B, particularly when combined with flucytosine, effectively clear fungal infections and help patients live longer.23467

Who Is on the Research Team?

TL

Thuy Le, MD, PhD

Principal Investigator

Duke University

Are You a Good Fit for This Trial?

This trial is for individuals with HIV-associated talaromycosis, a fungal infection. Participants must meet certain health criteria to join, but specific inclusion and exclusion details are not provided here.

Inclusion Criteria

I am an adult with HIV, with or without antiretroviral therapy.
My infection has been confirmed by lab tests.

Exclusion Criteria

Known severe allergy to AmB or 5FC
Absolute neutrophil count less than 500 cells
Pregnancy
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Induction Treatment

Participants receive either a single 10 mg/kg dose of liposomal amphotericin B (LAmB) or 14 days of deoxycholate amphotericin B (DAmB), with or without flucytosine (5FC)

14 days
Daily visits for 14 days

Maintenance Therapy

Participants receive itraconazole maintenance therapy, guided by either HIV viral load or CD4 count

12 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

24 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Flucytosine
  • Liposomal Amphotericin B
Trial Overview The LAmB-FAST trial is testing whether a single dose of Liposomal Amphotericin B (LAmB) is more effective than the standard 14-day treatment with Deoxycholate Amphotericin B (DAmB), and if adding Flucytosine (5FC) improves outcomes. It also examines different strategies for stopping maintenance therapy to prevent relapse.
How Is the Trial Designed?
4Treatment groups
Experimental Treatment
Active Control
Group I: Liposomal Amphotericin B (LAmB) plus Flucytosine (5FC) placeboExperimental Treatment2 Interventions
Group II: Liposomal Amphotericin B (LAmB) plus Flucytosine (5FC)Experimental Treatment2 Interventions
Group III: Deoxycholate Amphotericin B (DAmB) plus Flucytosine (5FC)Experimental Treatment2 Interventions
Group IV: Deoxycholate Amphotericin B (DAmB) plus Flucytosine (5FC) placeboActive Control2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Duke University

Lead Sponsor

Trials
2,495
Recruited
5,912,000+

Pham Ngoc Thach University of Medicine

Collaborator

Trials
5
Recruited
2,700+

Maharat Nakhon Ratchasima Hospital

Collaborator

Trials
3
Recruited
3,800+

Chiang Mai University

Collaborator

Trials
136
Recruited
36,800+

Bach Mai Hospital

Collaborator

Trials
10
Recruited
29,300+

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam

Collaborator

Trials
23
Recruited
16,500+

Viatris Inc.

Industry Sponsor

Trials
11
Recruited
5,600+

National Hospital for Tropical Diseases, Hanoi, Vietnam

Collaborator

Trials
12
Recruited
12,500+

Gilead Sciences

Industry Sponsor

Trials
1,150
Recruited
878,000+
Daniel O'Day profile image

Daniel O'Day

Gilead Sciences

Chief Executive Officer since 2019

MBA from Columbia University

Dietmar Berger profile image

Dietmar Berger

Gilead Sciences

Chief Medical Officer

MD and PhD from Albert-Ludwigs University School of Medicine

Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Collaborator

Trials
3
Recruited
10,500+

Published Research Related to This Trial

Lipid formulations of amphotericin B, such as liposomal amphotericin B, show reduced renal toxicity compared to traditional amphotericin B deoxycholate, but no formulation has demonstrated superior efficacy in well-designed studies.
A recent study found that while a standard dose of liposomal amphotericin B showed a numerically better response rate for treating invasive fungal infections compared to a higher loading dose, the increased nephrotoxicity in the loading dose group suggests it should not be used in clinical practice.
[Lipid formulations of amphotericin B in the management of invasive fungal infections].Fohrer, C., Nivoix, Y., Moulin, JC., et al.[2019]

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/38943665/
Comparison of Early Fungicidal Activity and Mortality Between ...Daily liposomal amphotericin B induction demonstrated a similar rate of CSF fungal clearance and 10-week mortality as amphotericin B deoxycholate.
Combination Antifungal Therapy for Cryptococcal MeningitisAmphotericin B plus flucytosine, as compared with amphotericin B alone, is associated with improved survival among patients with cryptococcal meningitis.
Comparison of amphotericin B deoxycholate in combination ...Our results suggest that AmB-D combined with 5FC remains the more efficacious induction regimen compared to AmB-D plus Flu, and that VCZ + 5FC might be a ...
A Substudy of the EnACT Trial Testing Oral AmphotericinThis trial demonstrated that a 1-week regimen of amphotericin B deoxycholate had fewer adverse events than and efficacy similar to a 2-week amphotericin B ...
Toxicity of Amphotericin B Deoxycholate-Based Induction ...Treatment with AmBd at a dose of 1 mg/kg of body weight/day plus 5FC provided the best fungal clearance and 10-week survival rates in a recent phase III trial ( ...
Amphotericin B - StatPearls - NCBI Bookshelf - NIHAmphotericin B lipid complex (ABLC) has received FDA approval for treating invasive fungal infections in patients who have shown resistance to ...
High-Dose Amphotericin B with Flucytosine for the Treatment ...AmB (at 1 mg/kg per day) is commonly used in practice for many fungal infections and has been administered with flucytosine for treatment of CM for the initial ...
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security