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VFEND® I.V., Oral
VFEND® I.V., Oral is an antifungal medication that inhibits the synthesis of ergosterol, an essential component of fungal cell membranes.
VFEND® I.V., Oral is an antifungal medication that inhibits the synthesis of ergosterol, an essential component of fungal cell membranes. Used for Treatment of invasive aspergillosis, invasive candidiasis, and esophageal candidiasis.
At a glance
| Generic name | VFEND® I.V., Oral |
|---|---|
| Sponsor | Pfizer |
| Drug class | Azole antifungal |
| Target | Lanosterol 14α-demethylase |
| Modality | Small molecule |
| Therapeutic area | Infectious Disease |
| Phase | Phase 3 |
Mechanism of action
VFEND® I.V., Oral works by targeting the enzyme lanosterol 14α-demethylase, which is necessary for the conversion of lanosterol to ergosterol. This inhibition disrupts the integrity of the fungal cell membrane, ultimately leading to cell death. As a result, VFEND® I.V., Oral is effective against a wide range of fungal infections.
Approved indications
- Treatment of invasive aspergillosis, invasive candidiasis, and esophageal candidiasis
Common side effects
- Headache
- Nausea
- Vomiting
- Diarrhea
- Abdominal pain
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.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |