New Data on Curetis’ Unyvero LRT Panel for Pneumonia to be Presented at ASM Microbe 2019
- Several scientific conference contributions outline benefits of U.S. FDA-cleared Unyvero LRT Application Cartridge in both endotracheal aspirate and bronchoalveolar lavage samples
- Study shows that Unyvero LRT has potential to support antibiotic stewardship and may reduce time to actionable clinical results by more than two days
Amsterdam, the Netherlands, San Diego, CA, USA, and Holzgerlingen, Germany, June 04, 2019 - Curetis N.V. (the "Company" and, together with Curetis GmbH and Curetis USA Inc. "Curetis"), a developer of next-level molecular diagnostic solutions, today announced that new data on its Unyvero System and LRT Application Cartridge for pneumonia will be presented at the upcoming ASM Microbe Conference, June 20-24, 2019, in San Francisco, CA, USA.
The potential of Unyvero LRT to support antibiotic stewardship and positively impact clinical outcomes is substantiated by several key contributions to the scientific program of ASM Microbe 2019:
- Dr. Joseph M. Campos, PhD, D(ABMM), F(AAM), Children’s National Medical Center, Washington, DC, will present the performance evaluation of the Unyvero LRT panel for pneumonia on bronchoalveolar lavage (BAL) and endotracheal aspirate (ETA) specimens obtained from pediatric patients. The findings highlight that the Unyvero LRT improved the detection of important and difficult-to-treat pathogens such as Pseudomonas and Acinetobacter. They conclude that ‘the qualitative reporting scheme of the Unyvero LRT results was unbiased and straightforward, enabling clinicians to manage patients with early interventions and avoid ineffective antimicrobial therapy.’ This poster is also featured as an oral presentation by Dr. Campos during the symposium "Novel Diagnostics for Pneumonia" on Saturday, June 22.
- Dr. Matthew D. Sims, MD, PhD, Beaumont Health, Royal Oak, MI, will present an evaluation of the Unyvero LRT panel on bronchoalveolar lavage (BAL) specimens obtained from patients suspected of pneumonia. The data demonstrated excellent overall sensitivity (93%) and specificity (98%) compared to microbiology culture, and importantly, Unyvero LRT detected pathogens that were missed by culture. Furthermore, Dr. Sims concludes that ‘Unyvero reduced the time from specimen arrival in the laboratory to actionable results by more than 2 days, providing significant potential to reduce the time to appropriate diagnosis of pneumonia.’
- In addition, in an Industry and Science Workshop hosted by Curetis USA, Dr. David W. Craft, PhD, D(ABMM), Professor of Pathology and Medical Director of Microbiology at Penn State Hershey Medical Center, will share early results from the evaluation of the Unyvero LRT panel on sputum and tracheal aspirates compared against conventional culture methods and will discuss the implications of the rapid test results on conventional diagnostic work-ups and the potential impact on the therapeutic management of patients by reporting these results into the electronic medical record.
“We are delighted about the growing amount of excellent clinical and scientific data on our Unyvero System and LRT Cartridge,” said Faranak Atrzadeh, Senior VP of Scientific Affairs of Curetis. “Most importantly, the recent results confirm that Unyvero may lead to a significantly faster diagnosis and enable informed treatment decisions more than two days earlier than standard microbiology culture.”
The Unyvero LRT Application Cartridge for pneumonia was cleared by the U.S. FDA in April 2018 and launched in the U.S. market at ASM Microbe Conference 2018. Initially cleared for use with tracheal aspirates as a sample type, Curetis is currently in the final stages of preparing a U.S. FDA submission for the clearance of the Unyvero LRT Application Cartridge for bronchoalveolar lavages (BAL), another sample type commonly used in the diagnosis of pneumonia. The submission builds on excellent recent performance data from clinical evaluation studies, which will be presented by Dr. Matthew D. Sims, MD, PhD, in his poster presentation at ASM Microbe 2019.
Curetis at ASM Microbe 2019
Curetis invites ASM Microbe 2019 attendees to visit the Curetis booth (#1236) for a demonstration of Unyvero LRT and discussing its clinical benefits supported by the recent study data and wealth of previous studies.
Unyvero LRT Presentations and Posters at ASM Microbe 2019
Industry and Science Workshop: Evaluation of the Curetis Unyvero Lower Respiratory Tract (LRT) Panel for Pneumonia in the Clinical Microbiology Laboratory of a Tertiary Care Teaching Hospital
D. W. Craft; Penn State Hershey Medical Center, Hershey, PA
June 20, 4:00 – 4:45PM PDT, Room 205/206, The George R. Moscone Convention Center
Poster 4617: Use of a Multiplex PCR Pneumonia Panel for the Microbial Analysis of Lower Respiratory Tract Specimens from Children
J. M. Campos, C. Guray; Children’s National Medical Center, Washington, DC
Session CPHM12 – Molecular Diagnostics Using Multiplex Platforms; Poster Board Number CPHM-951
June 22, 11:00AM – 12:00PM and 4:00 – 5:00PM, Exhibit and Poster Hall
Poster 4899: Evaluation of a Rapid Highly Multiplexed Molecular Diagnostic Lower Respiratory Tract Panel for Use with Bronchoalveolar Lavage Specimens
K. Powell, M. Sims; Beaumont Health, Royal Oak, MI
Session CPHM12 – Molecular Diagnostics Using Multiplex Platforms; Poster Board Number CPHM-953
June 22, 11:00AM – 12:00PM and 4:00 – 5:00PM, Exhibit and Poster Hall
Oral Abstract Presentation: Use of a Multiplex PCR Pneumonia Panel for the Microbial Analysis of Lower Respiratory Tract Specimens from Children
J. M. Campos; Children’s National Medical Center, Washington, DC
Session Symposium – Novel Diagnostics for Pneumonia
June 22, 2:00 – 2:15PM, Room 213/214, The George R. Moscone Convention Center
Curetis N.V.’s (Euronext: CURE) goal is to become a leading provider of innovative solutions for molecular microbiology diagnostics designed to address the global challenge of detecting severe infectious diseases and identifying antibiotic resistances in hospitalized patients.
Curetis’ Unyvero System is a versatile, fast and highly automated molecular diagnostic platform for easy-to-use, cartridge-based solutions for the comprehensive and rapid detection of pathogens and antimicrobial resistance markers in a range of severe infectious disease indications. Results are available within hours, a process that can take days or even weeks if performed with standard diagnostic procedures, thereby facilitating improved patient outcomes, stringent antibiotic stewardship and health-economic benefits. Unyvero in vitro diagnostic (IVD) products are marketed in Europe, the Middle East, Asia and the U.S.
Curetis’ wholly owned subsidiary Ares Genetics GmbH is developing next-generation solutions for infectious disease diagnostics and therapeutics. The ARES Technology Platform combines the presumably most comprehensive database worldwide on the genetics of antimicrobial resistances, ARESdb, with advanced bioinformatics and artificial intelligence.
This document constitutes neither an offer to buy nor an offer to subscribe for securities and neither this document nor any part of it should form the basis of any investment decision in Curetis.
The information contained in this press release has been carefully prepared. However, Curetis bears and assumes no liability of whatever kind for the correctness and completeness of the information provided herein. Curetis does not assume an obligation of whatever kind to update or correct information contained in this press release whether as a result of new information, future events or for other reasons.
This press release includes statements that are, or may be deemed to be, “forward-looking statements.” These forward-looking statements can be identified by the use of forward-looking terminology, including the terms “believes,” “estimates,” “anticipates,” “expects,” “intends,” “targets,” “may,” “will,” or “should” and include statements Curetis makes concerning the intended results of its strategy. By their nature, forward-looking statements involve risks and uncertainties and readers are cautioned that any such forward-looking statements are not guarantees of future performance. Curetis’ actual results may differ materially from those predicted by the forward-looking statements. Curetis undertakes no obligation to publicly update or revise forward-looking statements, except as may be required by law.
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