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Posaconazole oral suspension

Merck Sharp & Dohme LLC · Phase 3 active Small molecule

Posaconazole oral suspension is a Triazole antifungal Small molecule drug developed by Merck Sharp & Dohme LLC. It is currently in Phase 3 development for Prophylaxis of invasive Aspergillus and Candida infections in high-risk immunocompromised patients, Treatment of oropharyngeal candidiasis, Treatment of invasive fungal infections in immunocompromised patients. Also known as: MK-5592, SCH 056592, Noxafil®.

Posaconazole inhibits fungal cell membrane ergosterol synthesis by blocking lanosterol 14α-demethylase, disrupting fungal cell wall integrity.

Posaconazole inhibits fungal cell membrane ergosterol synthesis by blocking lanosterol 14α-demethylase, disrupting fungal cell wall integrity. Used for Prophylaxis of invasive Aspergillus and Candida infections in high-risk immunocompromised patients, Treatment of oropharyngeal candidiasis, Treatment of invasive fungal infections in immunocompromised patients.

At a glance

Generic namePosaconazole oral suspension
Also known asMK-5592, SCH 056592, Noxafil®
SponsorMerck Sharp & Dohme LLC
Drug classTriazole antifungal
TargetLanosterol 14α-demethylase (CYP51)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

As a triazole antifungal, posaconazole binds to the cytochrome P450-dependent enzyme lanosterol 14α-demethylase in fungi, preventing the conversion of lanosterol to ergosterol. This disrupts the fungal cell membrane structure, leading to cell lysis and fungal death. The oral suspension formulation provides improved bioavailability compared to earlier formulations.

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

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Frequently asked questions about Posaconazole oral suspension

What is Posaconazole oral suspension?

Posaconazole oral suspension is a Triazole antifungal drug developed by Merck Sharp & Dohme LLC, indicated for Prophylaxis of invasive Aspergillus and Candida infections in high-risk immunocompromised patients, Treatment of oropharyngeal candidiasis, Treatment of invasive fungal infections in immunocompromised patients.

How does Posaconazole oral suspension work?

Posaconazole inhibits fungal cell membrane ergosterol synthesis by blocking lanosterol 14α-demethylase, disrupting fungal cell wall integrity.

What is Posaconazole oral suspension used for?

Posaconazole oral suspension is indicated for Prophylaxis of invasive Aspergillus and Candida infections in high-risk immunocompromised patients, Treatment of oropharyngeal candidiasis, Treatment of invasive fungal infections in immunocompromised patients.

Who makes Posaconazole oral suspension?

Posaconazole oral suspension is developed by Merck Sharp & Dohme LLC (see full Merck Sharp & Dohme LLC pipeline at /company/merck).

Is Posaconazole oral suspension also known as anything else?

Posaconazole oral suspension is also known as MK-5592, SCH 056592, Noxafil®.

What drug class is Posaconazole oral suspension in?

Posaconazole oral suspension belongs to the Triazole antifungal class. See all Triazole antifungal drugs at /class/triazole-antifungal.

What development phase is Posaconazole oral suspension in?

Posaconazole oral suspension is in Phase 3.

What are the side effects of Posaconazole oral suspension?

Common side effects of Posaconazole oral suspension include Nausea, Vomiting, Diarrhea, Headache, Abdominal pain, Elevated liver enzymes.

What does Posaconazole oral suspension target?

Posaconazole oral suspension targets Lanosterol 14α-demethylase (CYP51) and is a Triazole antifungal.

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