FDA Approves Companion Diagnostic to Identify NSCLC Patients Eligible for Tepmetko
The tissue-based test identifies patients with MET exon 14 skipping alterations eligible for treatment with tepotinib.
Read MorePosted by CLP Edit Staff | May 22, 2026 | Lung Cancer, Molecular Diagnostics |
The tissue-based test identifies patients with MET exon 14 skipping alterations eligible for treatment with tepotinib.
Read MorePosted by CLP Edit Staff | May 22, 2026 | Cancer, Company News, Molecular Diagnostics |
The FDA has approved Guardant360 Liquid CDx, a blood-based test that integrates genomic and epigenomic profiling for advanced cancer, offering a broader genomic footprint and faster results.
Read MorePosted by CLP Edit Staff | May 21, 2026 | Accreditation, Company News, Prostate |
Cleveland Diagnostics has received ISO 13485:2016 certification for its IsoPSA Assay, supporting scaled U.S. commercialization following recent FDA approval for prostate cancer risk assessment.
Read MorePosted by CLP Edit Staff | May 18, 2026 | Diabetes & Metabolic Diseases |
As diabetes testing evolves, labs are seeing growing interest in earlier screening, additional biomarkers, and tools that can support more preventive care.
Read MorePosted by CLP Edit Staff | May 14, 2026 | Emerging & Zoonotic Diseases, Infectious Diseases, Molecular Diagnostics |
Eurofins companies are developing molecular and serological tests to monitor a hantavirus outbreak linked to the Andes strain, with 11 cases and three deaths reported as of May 12.
Read More