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Brexafemme (IBREXAFUNGERP CITRATE)

GSK · FDA-approved approved Small molecule Quality 27/100

Brexafemme (generic name: IBREXAFUNGERP CITRATE) is a Triterpenoid Antifungal Small molecule drug developed by GSK. It is currently FDA-approved (first approved 2021) for Candidiasis of vagina, Vulvovaginal candidiasis.

At a glance

Generic nameIBREXAFUNGERP CITRATE
SponsorGSK
Drug classTriterpenoid Antifungal
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved
First approval2021

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Patents

PatentExpiryType

Primary sources

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

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

Competitive intelligence

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Frequently asked questions about Brexafemme

What is Brexafemme?

Brexafemme (IBREXAFUNGERP CITRATE) is a Triterpenoid Antifungal drug developed by GSK, indicated for Candidiasis of vagina, Vulvovaginal candidiasis.

What is Brexafemme used for?

Brexafemme is indicated for Candidiasis of vagina, Vulvovaginal candidiasis.

Who makes Brexafemme?

Brexafemme is developed and marketed by GSK (see full GSK pipeline at /company/gsk).

What is the generic name of Brexafemme?

IBREXAFUNGERP CITRATE is the generic (nonproprietary) name of Brexafemme.

What drug class is Brexafemme in?

Brexafemme belongs to the Triterpenoid Antifungal class. See all Triterpenoid Antifungal drugs at /class/triterpenoid-antifungal.

When was Brexafemme approved?

Brexafemme was first approved on 2021.

What development phase is Brexafemme in?

Brexafemme is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing