Anidulafungin
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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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL264241 |
| Name | Anidulafungin |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 166548 |
| ChEBI | CHEBI:55346 |
| ATC | J02AX06 |
| Molecular formula | C58H73N7O17 |
| Molecular weight | 1140.2 |
| InChIKey | JHVAMHSQVVQIOT-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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| candidemia | 4 | MONDO:0044070 | EFO:1001282 |
| infectious peritonitis | 4 | MONDO:0004522 | EFO:0008588 |
| candidiasis | 4 | MONDO:0002026 | MONDO:0002026 |
| aspergillosis | 3 | MONDO:0005657 | EFO:0007157 |
| candidiasis, invasive | 3 | MONDO:0044067 | EFO:1001283 |
| neuroaspergillosis | 3 | MONDO:0005873 | EFO:0007393 |
| myelodysplastic syndrome | 2 | MONDO:0018881 | EFO:0000198 |
| acute myeloid leukemia | 2 | MONDO:0018874 | EFO:0000222 |
| neoplasm | 2 | MONDO:0005070 | MONDO:0004992 |
| leukemia | 2 | MONDO:0005059 | EFO:0000565 |
| neutropenia | 1 | MONDO:0001475 | MONDO:0001475 |
| fungal infectious disease | 1 | MONDO:0002041 | MONDO:0002041 |
Clinical trials
Total trials: 30.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 11 |
| PHASE4 | 8 |
| PHASE2 | 5 |
| PHASE1/PHASE2 | 2 |
| Not specified | 2 |
| PHASE2/PHASE3 | 1 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00496197 | PHASE4 | COMPLETED | Study Will Evaluate The Safety And Efficacy Of Anidulafungin In Patients With Candidemia Or Invasive Candidiasis |
| NCT00548262 | PHASE4 | COMPLETED | This 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 |
| NCT00620074 | PHASE4 | TERMINATED | Study 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) |
| NCT00841971 | PHASE4 | COMPLETED | Anidulafungin Versus Fluconazole for the Prevention of Fungal Infections in Liver Transplant Recipients |
| NCT00940017 | PHASE4 | COMPLETED | A Study To Assess The Anidulafungin And Voriconazole Concentration In Lung Following Intravenous Administration In Healthy Subjects |
| NCT01303549 | PHASE4 | COMPLETED | Anidulafungin vs Amphotericin B Safety in High Risk Hepatic Transplant Recipients |
| NCT01307930 | PHASE4 | COMPLETED | Effect of Weight and/or Obesity on Anidulafungin Drug Concentrations |
| NCT01734525 | PHASE4 | COMPLETED | Negative Beta Glucan in ICU Patients |
| NCT00037206 | PHASE2/PHASE3 | COMPLETED | A Safety & Effectiveness Study of Intravenous Anidulafungin With AmBisome® for Treatment of Invasive Aspergillosis (IA). |
| NCT00056368 | PHASE3 | COMPLETED | The Safety and Efficacy of Anidulafungin Versus Comparator in Patients With Candidemia and Invasive Candidiasis |
| NCT00058682 | PHASE3 | COMPLETED | Anidulafungin Versus Fluconazole in the Treatment of Candidemia |
| NCT00531479 | PHASE3 | COMPLETED | Anidulafungin Plus Voriconazole Versus Voriconazole For The Treatment Of Invasive Aspergillosis |
| NCT00537329 | PHASE3 | COMPLETED | Anidulafungin In Treatment Of Candidemia In Asian Subjects |
| NCT00689338 | PHASE3 | COMPLETED | Anidulafungin Candidemia/Invasive Candidiasis Intensive Care Study |
| NCT00761267 | PHASE3 | COMPLETED | Study To Assess Pharmacokinetics, Safety & Efficacy of Anidulafungin When Treating Children With Invasive Candidiasis |
| NCT00805740 | PHASE3 | TERMINATED | An Evaluation Of The Effectiveness And Safety Of Anidulafungin Compared To Caspofungin For The Treatment Of Deep Tissue Infection Due To Candida |
| NCT00806351 | PHASE3 | TERMINATED | An 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 |
| NCT01176058 | PHASE3 | TERMINATED | A Study Of The Efficacy And Safety Of Anidulafungin Vs. Fluconazole In The Treatment Of Patients With Candidemia And/Or Other Forms Of Invasive Candidiasis |
| NCT01188759 | PHASE3 | WITHDRAWN | Voriconazole And Anidulafungin Combination For Invasive Aspergillosis In Pediatric Subjects |
| NCT04876716 | PHASE3 | TERMINATED | Azole-echinocandin Combination Therapy for Invasive Aspergillosis |
| NCT00037219 | PHASE2 | COMPLETED | The Safety and Effectiveness of Intravenous Anidulafungin as a Treatment for Patients With Invasive Candidiasis. |
| NCT00041704 | PHASE2 | COMPLETED | The Safety and Efficacy of Intravenous Anidulafungin as a Treatment for Azole-Refractory Mucosal Candidiasis (FRMC) |
| NCT00056381 | PHASE1/PHASE2 | COMPLETED | Safety, Tolerance and Pharmacokinetics of Anidulafungin in Immunocompromised Children Ages 2-17 |
| NCT00068471 | PHASE1/PHASE2 | COMPLETED | Anidulafungin in Treating Immunocompromised Children With Neutropenia |
| NCT00892359 | PHASE2 | UNKNOWN | Anidulafungin During Continuous Venovenous Hemofiltration (CVVHF) |
| NCT00934934 | PHASE2 | TERMINATED | Candida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment |
| NCT01053884 | PHASE2 | TERMINATED | Anidulafungin in Patients With Hematologic Malignancies |
| NCT00734500 | PHASE1 | COMPLETED | Anidulafungin PK in Infants and Toddlers |
| NCT00491426 | Not specified | COMPLETED | Antimicrobial PK in Infants With Suspected or Confirmed Infection |
| NCT01202253 | Not specified | COMPLETED | Early 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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).