Table 3.
Antifungal Product Type in the Pipeline, Pathogen, Phase of Clinical Trial and Expected Activity Against Fusarium
Pathogen | Compound (Notes) | Company | Development Status | Antifungal Class | Activity (MIC μg/mL) | Related Ref.s |
---|---|---|---|---|---|---|
Fusarium | Isavuconazole | Astellas Pharma, US, Inc. – License holder Basilea Pharmaceu., Switzerland – outside USA and Canada | FDA approves new antifungal drug Cresemba (Oral/IV) March 6, 2015 | Triazole | Variable from 1 to ≥16 | 70 |
Efinaconazole (KP-103) | JUBLIA® Valeant Pharmaceu., Canada | FDA approval: September 2014 Topical 10% | Triazole | 0.85 | 83 | |
Luliconazole (NND-502) | Nihon Nohyaku Co Ltd (Osaka, Japan) | Approved, USA, Nov 15, 2013 Cream 1%, solution 10% | Imidazole | 0.005 | 83 | |
Lanoconazole | Nihon Nohyaku Co Ltd (Osaka, Japan) | Approved, USA, Nov 15, 2013 Cream 1%, solution 10% | Imidazole | 0.013 | 83 | |
AR-12 celecoxib derivative | Arno Therapeutics, Flemington, NJ, USA) | - | Celecoxib Derivative | 4 | 89 | |
F901318 = Olorofim | F2G, Manchester, UK | Phase 2 Preclinical | Orotomides | 1 to 2 | 93 | |
E1210 Inositol acyltransferase inhibitor Oral | Eisai Co., Japan | Preclinical | - | −0.015–0.25 -0.12 |
94 | |
SCY078 (formerly MK-3118) IV/Oral | Scynexis, Durham, NC, USA | Phase 2 | Triterpene/Enfumafungin derivative | poor activity | 97 | |
T-2307 Arylamidine derivatives | Toyama, Japan | Preclinical | Arylamidine derivatives | 0.125 | 99 | |
MGCD290 Oral histone deacetylase inhibitor | Mirati Therapeu., CA, USA | Phase 2 | Hos2 histone deacetylase inhibitor | Effective in combination | 101 |