FDA-Cleared Molecular Test Targets Growing US Cyclospora Outbreak
QIAGEN’s FDA-cleared QIAstat-Dx panel detects Cyclospora cayetanensis, addressing a surge of over 1,600 confirmed US cases since May 2026.
QIAGEN’s FDA-cleared QIAstat-Dx panel detects Cyclospora cayetanensis, addressing a surge of over 1,600 confirmed US cases since May 2026.
The point-of-care assay provides results in 15 minutes and received a waiver for use in decentralized settings.
ARUP Laboratories has launched a dashboard tracking national infectious disease test positivity trends, using deidentified lab data to help clinical labs and medical directors identify emerging patterns and seasonal shifts.
A field-deployable test demonstrates high sensitivity in identifying low-level infections that traditional methods miss, potentially supporting elimination efforts.
The high-throughput host-response assay provides results in approximately 20 minutes to help guide treatment decisions and antimicrobial stewardship.
The PCR test detects 11 bacterial, viral, and parasitic pathogens from a stool sample in approximately 74 minutes.
Research identifies how circulating tumor DNA can inform personalized treatment and surveillance strategies.