Amphotericin B
FDA-approved product (ointment, topical), marketed as Abelcet, Ambisome, Amphotec and 2 more.
- Registered studies
- 50+
- Lab records
- 1
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Aspergillosis
- Candidiasis
- Cryptococcal meningitis
- Cryptococcosis
- Fungal infectious disease
- Histoplasmosis
- Infection
- Mucormycosis
- Sporotrichosis
- Visceral Leishmaniasis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antiinfectives and antiseptics for local oral treatment; Antibiotics
- FDA pharmacologic class
- Lipid-based Polyene Antifungal; Polyene Antifungal FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC A01AB04; WHO ATC A07AA07; WHO ATC G01AA03; WHO ATC J02AA01; FDA class Lipid-based Polyene Antifungal; FDA class Polyene Antifungal
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis and MRSA. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA54.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli39.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae20.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- M. tuberculosis51.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
- K. pneumoniae: measured active in 0 of 1 lab record
Show the 1 laboratory record, with sources
Loading records…
“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Amphotericin B with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- DichlorphenamideExisting use: Glaucoma73.9% AI-predicted activityagainst M. tuberculosisLab records exist2 registered studies
- Tamsulosin HydrochlorideExisting use: Benign prostatic hyperplasia, Prostate carcinoma73.2% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Thiethylperazine MalateExisting use: Allergic disease71.8% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SaquinavirExisting use: HIV infection, HIV-1 infection, Viral disease71.5% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AvacopanExisting use: Anti-neutrophil antibody associated vasculitis, Anti-neutrophil cytoplasmic antibody-associated vasculitis, Granulomatosis with Polyangiitis and 1 more71.3% AI-predicted activityagainst M. tuberculosis26 registered studies
- Lasmiditan SuccinateExisting use: Migraine disorder71.0% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma71.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Vinblastine SulfateExisting use: Classic Hodgkin lymphoma, Fungal infectious disease, Hodgkins lymphoma and 3 more70.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Haloperidol DecanoateExisting use: Conduct disorder, Mental or behavioural disorder, Psychosis and 4 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- HydrochlorothiazideExisting use: Angina pectoris, Cardiovascular disease, Chronic kidney disease and 9 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- TolvaptanExisting use: Autosomal dominant polycystic kidney disease, Cardiovascular disease, Congestive heart failure and 4 more70.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more69.2% AI-predicted activityagainst M. tuberculosis5 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Three Induction Treatments on Cryptococcal Meningitis
NCT04072640 · start 2021-01-25
Registered record
- Registry ID
- NCT04072640
- Conditions
- Cryptococcal Meningitis; HIV/AIDS
- Interventions
- Voriconazole 200mg; amphotericin B deoxycholate (0.4-0.5mg/kg/d); Amphotericin B-deoxycholate (0.7-1.0mg/kg/d)
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Unknown
- Start
- 2021-01-25
- Completion
- 2022-12-01
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCryptococcal Meningitis; HIV/AIDSInterventionVoriconazole 200mg; amphotericin B deoxycholate (0.4-0.5mg/kg/d); Amphotericin B-deoxycholate (0.7-1.0mg/kg/d)PhaseEarly phase 1Registry statusUnknownClinical Effectiveness and Safety of Amphotericin B With Flucytosine-Fluconazole Therapy for Cryptococcal Meningitis
NCT04532463 · start 2020-10-01
Registered record
- Registry ID
- NCT04532463
- Conditions
- Cryptococcal Meningitis
- Interventions
- Amphotericin B 1 mg/kg 1 week & Flucytosine 100 mg/kg 1 week followed by Fluconazole 1200 mg/day 1 week
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2020-10-01
- Completion
- 2022-04-20
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCryptococcal MeningitisInterventionAmphotericin B 1 mg/kg 1 week & Flucytosine 100 mg/kg 1 week followed by Fluconazole 1200 mg/day 1 weekPhaseNot recordedRegistry statusCompletedPharmacokinetics and Safety of AmBisome and DKF-5122
NCT05749380 · start 2020-09-07
Registered record
- Registry ID
- NCT05749380
- Conditions
- Invasive Fungal Infections; Neutropenic Fever
- Interventions
- AmBisome; DKF-5122
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2020-09-07
- Completion
- 2022-01-28
- Enrolment
- 38
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInvasive Fungal Infections; Neutropenic FeverInterventionAmBisome; DKF-5122PhasePhase 1Registry statusCompletedCombined Inhalational With Intravenous Amphotericin B Versus Intravenous Amphotericin B Alone for Pulmonary Mucormycosis
NCT04502381 · start 2020-07-01
Registered record
- Registry ID
- NCT04502381
- Conditions
- Pulmonary Mucormycosis
- Interventions
- Inhaled amp B deoxycholate+intravenous liposomal amp B; Intravenous liposomal amphotericin B alone
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2020-07-01
- Completion
- 2021-12-30
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary MucormycosisInterventionInhaled amp B deoxycholate+intravenous liposomal amp B; Intravenous liposomal amphotericin B alonePhasePhase 2Registry statusCompletedA Pilot Bioequivalence Study Between Amphotericin B Liposome for Injection and AmBisome® in Healthy Subjects
NCT04993222 · start 2020-06-04
Registered record
- Registry ID
- NCT04993222
- Conditions
- Bioequivalence
- Interventions
- Amphotericin B liposome for injection; AmBisome®
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2020-06-04
- Completion
- 2020-11-16
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBioequivalenceInterventionAmphotericin B liposome for injection; AmBisome®PhasePhase 1Registry statusCompletedEffect of Topical Sinonasal Antibiotics
NCT03935828 · start 2019-06
Registered record
- Registry ID
- NCT03935828
- Conditions
- Chronic Rhinosinusitis (Diagnosis); Antibiotic Side Effect
- Interventions
- Oral versus topical antibioitics
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2019-06
- Completion
- 2021-06
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Rhinosinusitis (Diagnosis); Antibiotic Side EffectInterventionOral versus topical antibioiticsPhasePhase 2Registry statusWithdrawnSingle Dose Escalations Study of Amphotericin B Colloidal Dispersion In Healthy Subjects in China
NCT03577509 · start 2018-07-02
Registered record
- Registry ID
- NCT03577509
- Conditions
- Invasive Fungal Disease
- Interventions
- ABCD
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2018-07-02
- Completion
- 2018-09-14
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInvasive Fungal DiseaseInterventionABCDPhasePhase 1Registry statusCompletedLiposomal Amphotericin B (AmBisome) Pharmacokinetics Given as a Single Intravenous Dose to Obese Patients (ASPEN)
NCT02320604 · start 2018-03-22
Registered record
- Registry ID
- NCT02320604
- Conditions
- Morbid Obesity
- Interventions
- Administration of study drug
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2018-03-22
- Completion
- 2018-11-03
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMorbid ObesityInterventionAdministration of study drugPhasePhase 4Registry statusCompletedAn Individualized Administration Research of Voriconazole Based on CYP2C19 Gene Polymorphism and TDM
NCT04004078 · start 2018-03-01
Registered record
- Registry ID
- NCT04004078
- Conditions
- Invasive Fungal Infection
- Interventions
- other antifungal agents,breathing machine
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2018-03-01
- Completion
- 2021-05-01
- Enrolment
- 314
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInvasive Fungal InfectionInterventionother antifungal agents,breathing machinePhaseNot recordedRegistry statusCompletedTopical Liposomal Amphotericin B Gel Treatment for Cutaneous Leishmaniasis
NCT02656797 · start 2018-01-30
Registered record
- Registry ID
- NCT02656797
- Conditions
- Leishmaniasis
- Interventions
- Topical Amphotericin-B 0.4% liposomal gel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2018-01-30
- Completion
- 2021-10-01
- Enrolment
- 13
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLeishmaniasisInterventionTopical Amphotericin-B 0.4% liposomal gelPhasePhase 2Registry statusCompletedSafety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
NCT02971007 · start 2016-11
Registered record
- Registry ID
- NCT02971007
- Conditions
- Vulvovaginitis; Yeast Infection; Yeast Infection Vaginal; Candidiasis, Vulvovaginal
- Interventions
- Oral Encochleated Amphotericin B (CAMB); Fluconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-11
- Completion
- 2017-05
- Enrolment
- 137
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionVulvovaginitis; Yeast Infection; Yeast Infection Vaginal; Candidiasis, VulvovaginalInterventionOral Encochleated Amphotericin B (CAMB); FluconazolePhasePhase 2Registry statusCompletedCAMB/MAT2203 in Patients With Mucocutaneous Candidiasis
NCT02629419 · start 2016-09-27
Registered record
- Registry ID
- NCT02629419
- Conditions
- Candidiasis, Chronic Mucocutaneous
- Interventions
- Amphotericin B
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-09-27
- Completion
- 2022-08-06
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCandidiasis, Chronic MucocutaneousInterventionAmphotericin BPhasePhase 2Registry statusCompletedSingle Dose Liposomal Amphotericin B for Visceral Leishmaniasis
NCT01566552 · start 2014-06
Registered record
- Registry ID
- NCT01566552
- Conditions
- Visceral Leishmaniasis
- Interventions
- AMBISOME
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2014-06
- Completion
- 2017-12
- Enrolment
- 1,300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionVisceral LeishmaniasisInterventionAMBISOMEPhasePhase 4Registry statusUnknownDoes Administration of Antibiotics in Patients Undergoing Surgery for Colorectal Cancer Result in Less Complications and Better Prognosis?
NCT01740947 · start 2013-01
Registered record
- Registry ID
- NCT01740947
- Conditions
- Colorectal Cancer
- Interventions
- Selective decontamination of the digestive tract (SDD) (colistin sulfate, tobramycin, amphotericin B)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2013-01
- Completion
- 2017-03
- Enrolment
- 485
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColorectal CancerInterventionSelective decontamination of the digestive tract (SDD) (colistin sulfate, tobramycin, amphotericin B)PhasePhase 4Registry statusTerminatedAn Bioequivalence Study to Compare Two 2 mg/ml Liposomal Amphotericin B Injections in Healthy Subjects
NCT01652859 · start 2012-02
Registered record
- Registry ID
- NCT01652859
- Conditions
- Normal Healthy Subjects
- Interventions
- Liposomal Amphotericin B; AmBisome
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2012-02
- Completion
- 2012-12
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNormal Healthy SubjectsInterventionLiposomal Amphotericin B; AmBisomePhasePhase 1Registry statusCompleted