Anidulafungin

drug
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Also known as AnidulafunginaAnidulafungineD-70013D70013EcaltaEraxisLY-303366LY303366V-echinocandinVER-002VER002Echinocandin B analogueAnidulaunginly

Summary

Anidulafungin (CHEMBL264241) is an approved small molecule (ATC J02AX06); indicated across 12 conditions including candidemia and infectious peritonitis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J02AX06
  • Indications: 12 conditions
  • Clinical trials: 30
  • Chemistry: 1140.2 Da · C58H73N7O17

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL264241
NameAnidulafungin
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID166548
ChEBICHEBI:55346
ATCJ02AX06
Molecular formulaC58H73N7O17
Molecular weight1140.2
InChIKeyJHVAMHSQVVQIOT-MFAJLEFUSA-N

SMILES: CCCCCOC1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=C(C=C3)C(=O)N[C@H]4C[C@H]([C@H](NC(=O)[C@@H]5[C@H]([C@H](CN5C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]6C[C@H](CN6C(=O)[C@@H](NC4=O)[C@@H](C)O)O)[C@@H]([C@H](C7=CC=C(C=C7)O)O)O)[C@@H](C)O)C)O)O)O

IUPAC name: N-[(3S,6S,9S,11R,15S,18S,20R,21R,24S,25S,26S)-6-[(1S,2S)-1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-11,20,21,25-tetrahydroxy-3,15-bis[(1R)-1-hydroxyethyl]-26-methyl-2,5,8,14,17,23-hexaoxo-1,4,7,13,16,22-hexazatricyclo[22.3.0.09,13]heptacosan-18-yl]-4-[4-(4-pentoxyphenyl)phenyl]benzamide

ChEBI definition: A semisynthetic echinocandin anti-fungal drug. It is active against Aspergillus and Candida species and is used for the treatment of invasive candidiasis.

Also known as: Anidulafungin, Anidulafungina, Anidulafungine, D-70013, D70013, Ecalta, Eraxis, LY-303366, LY303366, V-echinocandin, VER-002, VER002

Parent form; salt/anhydrous children: CHEMBL1275711

Patent coverage: 2,300 distinct patent families (8,634 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Cytochrome P450 2C8.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

12 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
candidemia4MONDO:0044070EFO:1001282
infectious peritonitis4MONDO:0004522EFO:0008588
candidiasis4MONDO:0002026MONDO:0002026
aspergillosis3MONDO:0005657EFO:0007157
candidiasis, invasive3MONDO:0044067EFO:1001283
neuroaspergillosis3MONDO:0005873EFO:0007393
myelodysplastic syndrome2MONDO:0018881EFO:0000198
acute myeloid leukemia2MONDO:0018874EFO:0000222
neoplasm2MONDO:0005070MONDO:0004992
leukemia2MONDO:0005059EFO:0000565
neutropenia1MONDO:0001475MONDO:0001475
fungal infectious disease1MONDO:0002041MONDO:0002041

Clinical trials

Total trials: 30.

Phase distribution

PhaseTrials
PHASE311
PHASE48
PHASE25
PHASE1/PHASE22
Not specified2
PHASE2/PHASE31
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00496197PHASE4COMPLETEDStudy Will Evaluate The Safety And Efficacy Of Anidulafungin In Patients With Candidemia Or Invasive Candidiasis
NCT00548262PHASE4COMPLETEDThis Is An Open-Label, Non-Comparative Study Designed To Evaluate A Short Course Of IV Anidulafungin, Followed Optionally By Oral Voriconazole, For The Treatment Of Candidemia And Invasive Candidiasis
NCT00620074PHASE4TERMINATEDStudy to Test the Combination of Voriconazole and Anidulafungin in Patients Who Have, or Are Thought to Have, Invasive Aspergillosis and Who Are Unable to Take a Common Antifungal Therapy (Polyene)
NCT00841971PHASE4COMPLETEDAnidulafungin Versus Fluconazole for the Prevention of Fungal Infections in Liver Transplant Recipients
NCT00940017PHASE4COMPLETEDA Study To Assess The Anidulafungin And Voriconazole Concentration In Lung Following Intravenous Administration In Healthy Subjects
NCT01303549PHASE4COMPLETEDAnidulafungin vs Amphotericin B Safety in High Risk Hepatic Transplant Recipients
NCT01307930PHASE4COMPLETEDEffect of Weight and/or Obesity on Anidulafungin Drug Concentrations
NCT01734525PHASE4COMPLETEDNegative Beta Glucan in ICU Patients
NCT00037206PHASE2/PHASE3COMPLETEDA Safety & Effectiveness Study of Intravenous Anidulafungin With AmBisome® for Treatment of Invasive Aspergillosis (IA).
NCT00056368PHASE3COMPLETEDThe Safety and Efficacy of Anidulafungin Versus Comparator in Patients With Candidemia and Invasive Candidiasis
NCT00058682PHASE3COMPLETEDAnidulafungin Versus Fluconazole in the Treatment of Candidemia
NCT00531479PHASE3COMPLETEDAnidulafungin Plus Voriconazole Versus Voriconazole For The Treatment Of Invasive Aspergillosis
NCT00537329PHASE3COMPLETEDAnidulafungin In Treatment Of Candidemia In Asian Subjects
NCT00689338PHASE3COMPLETEDAnidulafungin Candidemia/Invasive Candidiasis Intensive Care Study
NCT00761267PHASE3COMPLETEDStudy To Assess Pharmacokinetics, Safety & Efficacy of Anidulafungin When Treating Children With Invasive Candidiasis
NCT00805740PHASE3TERMINATEDAn Evaluation Of The Effectiveness And Safety Of Anidulafungin Compared To Caspofungin For The Treatment Of Deep Tissue Infection Due To Candida
NCT00806351PHASE3TERMINATEDAn Evaluation Of The Effectiveness And Safety Of Anidulafungin Compared To Caspofungin For The Treatment Of Serious Fungal Infection Due To Candida In Patients With A Dysfunctional Immune System
NCT01176058PHASE3TERMINATEDA Study Of The Efficacy And Safety Of Anidulafungin Vs. Fluconazole In The Treatment Of Patients With Candidemia And/Or Other Forms Of Invasive Candidiasis
NCT01188759PHASE3WITHDRAWNVoriconazole And Anidulafungin Combination For Invasive Aspergillosis In Pediatric Subjects
NCT04876716PHASE3TERMINATEDAzole-echinocandin Combination Therapy for Invasive Aspergillosis
NCT00037219PHASE2COMPLETEDThe Safety and Effectiveness of Intravenous Anidulafungin as a Treatment for Patients With Invasive Candidiasis.
NCT00041704PHASE2COMPLETEDThe Safety and Efficacy of Intravenous Anidulafungin as a Treatment for Azole-Refractory Mucosal Candidiasis (FRMC)
NCT00056381PHASE1/PHASE2COMPLETEDSafety, Tolerance and Pharmacokinetics of Anidulafungin in Immunocompromised Children Ages 2-17
NCT00068471PHASE1/PHASE2COMPLETEDAnidulafungin in Treating Immunocompromised Children With Neutropenia
NCT00892359PHASE2UNKNOWNAnidulafungin During Continuous Venovenous Hemofiltration (CVVHF)
NCT00934934PHASE2TERMINATEDCandida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment
NCT01053884PHASE2TERMINATEDAnidulafungin in Patients With Hematologic Malignancies
NCT00734500PHASE1COMPLETEDAnidulafungin PK in Infants and Toddlers
NCT00491426Not specifiedCOMPLETEDAntimicrobial PK in Infants With Suspected or Confirmed Infection
NCT01202253Not specifiedCOMPLETEDEarly Clinical Experience With Anidulafungin In Patients With Liver Disease In The United Kingdom

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).