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Ambisome and Paromomycin

Drugs for Neglected Diseases · Phase 3 active Small molecule

Ambisome (liposomal amphotericin B) disrupts fungal cell membranes by binding ergosterol, while paromomycin is an aminoglycoside antibiotic that inhibits protein synthesis in parasites.

Ambisome (liposomal amphotericin B) disrupts fungal cell membranes by binding ergosterol, while paromomycin is an aminoglycoside antibiotic that inhibits protein synthesis in parasites. Used for Visceral leishmaniasis (kala-azar), Fungal infections in immunocompromised patients.

At a glance

Generic nameAmbisome and Paromomycin
SponsorDrugs for Neglected Diseases
Drug classAntifungal and antiparasitic combination
TargetFungal ergosterol; parasitic 30S ribosomal subunit
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Ambisome is a lipid formulation of amphotericin B that preferentially targets fungal ergosterol in cell membranes, causing membrane disruption and cell death while reducing toxicity to human cells. Paromomycin is an aminoglycoside that binds to the 30S ribosomal subunit of parasites, inhibiting protein synthesis. Together, this combination targets both fungal and parasitic pathogens, particularly in visceral leishmaniasis.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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