An Exosome-Based Liquid Biopsy for the Differential Diagnosis of Primary Liver Cancer
NCT06342414
Adenocarcinoma, Carcinoma
Duarte, California, United States
View Trial DetailsNCT Number: NCT02762721
The primary objective of this study is to estimate the frequency of FGFR2 fusions in archived intrahepatic cholangiocarcinoma (iCCA) or mixed hepatocellular-cholangiocarcinoma (HCC-CCA) tumor samples
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Notify Me18 year and older
All sexes
Observational
Rozzano, MI, Italy
This is a non-interventional, observational study of archived human tissue samples; no surgical procedures will be required and no treatment will be provided as part of this study. Approximately 150 archived tissue samples obtained from patients with iCCA or mixed HCC-CCA will be analyzed for somatic alteration status and will include cholangiocarcinoma-specific FGFR2 fusion isoforms.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Archived tumor samples will be collected through study completion, up to 18 months
Archived tumor samples will be collected and analyzed using a Next Generation Sequencing panel.
Time frame: Archived tumor samples will be collected through study completion, up to 18 months
Archived tumor samples will be collected and analyzed using a Next Generation Sequencing panel.
Time frame: Archived tumor samples will be collected through study completion, up to 18 months
Archived tumor samples will be collected and analyzed using a Next Generation Sequencing panel.
ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
Industry
Molecular Analysis of Oncogenes in Tumor Samples From Adult Patients With Intrahepatic Cholangiocarcinoma or Mixed Hepatocellular-Cholangiocarcinoma
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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