Last reviewed · How we verify

liposomal amphotericin B + miltefosine

Drugs for Neglected Diseases · Phase 3 active Small molecule

Liposomal amphotericin B targets fungal cell membranes, while miltefosine targets fungal cell membranes and inhibits sphingosine N-acyltransferase.

Liposomal amphotericin B targets fungal cell membranes, while miltefosine targets fungal cell membranes and inhibits sphingosine N-acyltransferase. Used for Visceral leishmaniasis.

At a glance

Generic nameliposomal amphotericin B + miltefosine
Also known asImpavido, AmBisome
SponsorDrugs for Neglected Diseases
Drug classAntifungal
TargetErgosterol, Sphingosine N-acyltransferase
ModalitySmall molecule
Therapeutic areaInfectious Diseases
PhasePhase 3

Mechanism of action

Liposomal amphotericin B works by binding to ergosterol in the fungal cell membrane, causing cell lysis and death. Miltefosine, on the other hand, inhibits the enzyme sphingosine N-acyltransferase, which is involved in the synthesis of sphingolipids, an essential component of fungal cell membranes. This dual mechanism of action makes liposomal amphotericin B + miltefosine a potent antifungal agent.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: