P-1194. Activity of manogepix against mould isolates collected from the US in 2023

Abstract Background Manogepix (MGX) is a novel agent targeting the fungal Gwt1 enzyme. This agent is undergoing phase 3 clinical trials for invasive candidiasis and mould infections. Here, we assessed the in vitro activity of MGX against US mould isolates from invasive infections. Methods A total of 94 mould isolates from 12 hospitals in 2023 were tested. Confirmatory identification was performed by MALDI-TOF or 28S sequencing. Isolates were tested by reference broth microdilution method according to CLSI guidelines against MGX, voriconazole (VRC), posaconazole (POS), isavuconazole (ISA), and amphotericin B (AMB). Susceptible, nonsusceptible (NS), wildtype (WT), or nonwildtype (NWT) isolates were identified applying CLSI breakpoints or epidemiological cutoff values (ECV). No breakpoints or ECVs are available for MGX. Results 27 mould species and 11 genera were represented (Figure 1). Source of infection was varied (Figure 2). For 44 Aspergillus fumigatus (AFUM), MGX MEC90 was 0.03 mg/L, 16 to 32-fold lower than MIC90 for azoles (Table 1). 6.8% of AFUM were NS to ISA and 11.4% NS to VRC. For VRC-NS AFUM (n = 5), MGX MECs were 0.008 – 0.03 mg/L. For 9 Aspergillus niger species complex (ANSC), MGX MECs were 0.004-0.015 mg/L, 64 to 500-fold lower than MIC for azoles. All ANSC isolates were WT to VRC and ISA. For 9 Fusarium spp., MGX MECs were 0.004 – 0.03 mg/L while all azoles had limited activity (MICs ≥ 4 mg/L). For 5 Scedosporium/Lomentospora, MGX MECs were 0.008 to 0.03 mg/L, comparator agent MICs were >500-fold higher. For the 8 Zygomycota (5 Rhizopus spp., 2 Mucor spp., and 1 Lichtheimia), MGX MECs ranged from 0.25 to 4 mg/L, which was similar to other comparators. Conclusion MGX has potent in vitro activity against mould isolates collected from invasive infections as part of a worldwide surveillance program. MGX has low MECs for challenging moulds including azole-R or azole-NWT Aspergillus spp. and Fusarium spp. and Scedosporium/Lomentospora spp. with elevated MICs to other agents. MGX is a promising novel antifungal agent for the treatment of invasive mould infections, including those caused by resistant isolates and warrants further development for clinical use. Disclosures Marisa Winkler, MD, PhD, Basilea: Advisor/Consultant|Basilea: Grant/Research Support|GSK: Advisor/Consultant|GSK: Grant/Research Support|Melinta Therapeutics: Advisor/Consultant|Melinta Therapeutics: Grant/Research Support|Mundipharma: Advisor/Consultant|Mundipharma: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Pulmocide: Advisor/Consultant|Pulmocide: Grant/Research Support Mariana Castanheira, PhD, Melinta Therapeutics: Advisor/Consultant|Melinta Therapeutics: Grant/Research Support

Authors

Institutions

Publication Details

Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.1387
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

P-1194. Activity of manogepix against mould isolates collected from the US in 2023

Abby L Klauer, Marisa Winkler, Paul R. Rhomberg, Samuel Edeker et al.
Open Forum Infectious Diseases
Antifungal resistance and susceptibility
article

P-1194. Activity of manogepix against mould isolates collected from the US in 2023

Abby L Klauer, Marisa Winkler, Paul R. Rhomberg, Samuel Edeker, Mariana Castanheira
article en

Abstract

Abstract Background Manogepix (MGX) is a novel agent targeting the fungal Gwt1 enzyme. This agent is undergoing phase 3 clinical trials for invasive candidiasis and mould infections. Here, we assessed the in vitro activity of MGX against US mould isolates from invasive infections. Methods A total of 94 mould isolates from 12 hospitals in 2023 were tested. Confirmatory identification was performed by MALDI-TOF or 28S sequencing. Isolates were tested by reference broth microdilution method according to CLSI guidelines against MGX, voriconazole (VRC), posaconazole (POS), isavuconazole (ISA), and amphotericin B (AMB). Susceptible, nonsusceptible (NS), wildtype (WT), or nonwildtype (NWT) isolates were identified applying CLSI breakpoints or epidemiological cutoff values (ECV). No breakpoints or ECVs are available for MGX. Results 27 mould species and 11 genera were represented (Figure 1). Source of infection was varied (Figure 2). For 44 Aspergillus fumigatus (AFUM), MGX MEC90 was 0.03 mg/L, 16 to 32-fold lower than MIC90 for azoles (Table 1). 6.8% of AFUM were NS to ISA and 11.4% NS to VRC. For VRC-NS AFUM (n = 5), MGX MECs were 0.008 – 0.03 mg/L. For 9 Aspergillus niger species complex (ANSC), MGX MECs were 0.004-0.015 mg/L, 64 to 500-fold lower than MIC for azoles. All ANSC isolates were WT to VRC and ISA. For 9 Fusarium spp., MGX MECs were 0.004 – 0.03 mg/L while all azoles had limited activity (MICs ≥ 4 mg/L). For 5 Scedosporium/Lomentospora, MGX MECs were 0.008 to 0.03 mg/L, comparator agent MICs were >500-fold higher. For the 8 Zygomycota (5 Rhizopus spp., 2 Mucor spp., and 1 Lichtheimia), MGX MECs ranged from 0.25 to 4 mg/L, which was similar to other comparators. Conclusion MGX has potent in vitro activity against mould isolates collected from invasive infections as part of a worldwide surveillance program. MGX has low MECs for challenging moulds including azole-R or azole-NWT Aspergillus spp. and Fusarium spp. and Scedosporium/Lomentospora spp. with elevated MICs to other agents. MGX is a promising novel antifungal agent for the treatment of invasive mould infections, including those caused by resistant isolates and warrants further development for clinical use. Disclosures Marisa Winkler, MD, PhD, Basilea: Advisor/Consultant|Basilea: Grant/Research Support|GSK: Advisor/Consultant|GSK: Grant/Research Support|Melinta Therapeutics: Advisor/Consultant|Melinta Therapeutics: Grant/Research Support|Mundipharma: Advisor/Consultant|Mundipharma: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Pulmocide: Advisor/Consultant|Pulmocide: Grant/Research Support Mariana Castanheira, PhD, Melinta Therapeutics: Advisor/Consultant|Melinta Therapeutics: Grant/Research Support

Open Forum Infectious DiseasesVol. 13(Supplement_1)
JMI Laboratories (US)
Openalex Percentile: Top 91%
Antifungal resistance and susceptibility
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.