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Clinical Trial Summary

The primary objective of this study, sponsored by Travera Inc. in Massachusetts, is to validate whether the mass response biomarker has potential to predict response of patients to specific therapies or therapeutic combinations using isolated tumor cells from various specimen formats including malignant fluids such as pleural effusions and ascites, core needle biopsies, fine needle aspirates, or resections.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Anus Neoplasms
  • Ascites
  • Ascites, Malignant
  • Breast Neoplasms
  • Carcinoma
  • Carcinoma Breast
  • Carcinoma of Esophagus
  • Carcinoma of the Appendix
  • Carcinoma of the Head and Neck
  • Carcinoma of the Oral Cavity
  • Carcinoma of the Oropharynx
  • Carcinoma of the Vulva
  • Carcinoma of Unknown Primary
  • Carcinoma, Hepatocellular
  • Carcinoma, Neuroendocrine
  • Carcinoma, Non-Small-Cell Lung
  • Carcinoma, Ovarian Epithelial
  • Carcinoma, Pancreatic
  • Carcinoma, Pancreatic Ductal
  • Carcinoma, Renal Cell
  • Carcinoma, Small Cell
  • Carcinoma, Thymic
  • Cholangiocarcinoma
  • Esophageal Neoplasms
  • Melanoma
  • Mesothelioma
  • Mesothelioma, Malignant
  • Nasopharyngeal Carcinoma
  • Pancreatic Cancer
  • Pleural Effusion
  • Pleural Effusion, Malignant
  • Thymoma
  • Urinary Bladder Neoplasms
  • Vulvar Neoplasms

NCT number NCT05461430
Study type Observational
Source Travera Inc
Contact Mark Stevens, Phd
Phone 6172999784
Email mstevens@travera.com
Status Recruiting
Phase
Start date July 15, 2022
Completion date July 2026

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