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Anidulafungin: A novel echinocandin

*Corresponding author for this work
  • Wayne State University
    ,
  • Henry Ford Health System
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Until recently, the treatment available for serious fungal infections was composed of amphotericin B and azoles, and each class demonstrated significant limitations. Echinocandins are a new class of drugs that have shown promising results in treating a variety of fungal infections. Of these, anidulafungin is a novel echinocandin that appears to have several advantages over existing antifungals. It is unique because it slowly degrades in humans, undergoing a process of biotransformation rather than being metabolized. It has potent in vitro activity against Aspergillus and Candida species, including those resistant to fluconazole or amphotericin B. Results of several clinical trials indicate that anidulafungin is effective in treating esophageal candidiasis, including azole-refractory disease. The results of a recent study comparing fluconazole versus anidulafungin demonstrated the superiority of anidulafungin in the treatment of candidemia and invasive candidiasis (IC). Studies evaluating the concomitant use of anidulafungin and either amphotericin B, voriconazole, or cyclosporine did not demonstrate significant drug-drug interactions or adverse events. To date, anidulafungin appears to have an excellent safety profile. On the basis of early clinical experience, it appears that anidulafungin will be a valuable asset in the management of serious and difficult-to-treat fungal infections.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 215-222 (8 pages)

Journal (Volume, Issue Number)

Clinical Infectious Diseases (Volume 43, Issue 2)

Publication milestones

  • Published - 07/15/2006

Publication status

Published - 07/15/2006

ISSN

1058-4838

Publication IDs

  • Scopus: 33745700391
  • PubMed: 16779750

Publication metrics

Metrics

SciVal
FWCI
3.80
SciVal
Author count
2
SciVal
citations
144
SciVal
Paper percentile
97
SciVal
Top percentile
5
Scopus
citations
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1

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Citation count
184
Captures
66

Funding Details

Potential conflicts of interest. J.A.V. has received recent research funding from Pfizer, Vicuron, Merck, Wyeth, Schering Plough, Cape Cod and Associates, and Fujisawa; has been a consultant for Fujisawa and Schering Plough; and has been on the speakers’ bureaus for Pfizer and Elan. J.D.S. has received recent research funding from Pfizer, has been a consultant for Vicuron and Pfizer, and has been on the speakers’ bureaus for Pfizer and Merck.