Mass Response of Tumor Cells as a Biomarker for Rapid Therapy Guidance (TraveraRTGx)

NCT05461430 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 72

Last updated 2026-04-13

No results posted yet for this study

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.

Conditions

  • Pleural Effusion, Malignant
  • Ascites, Malignant
  • Carcinoma
  • Carcinoma, Hepatocellular
  • Carcinoma, Renal Cell
  • Carcinoma, Renal
  • Carcinoma, Small Cell
  • Carcinoma, Non-Small-Cell Lung
  • Carcinoma, Pancreatic Ductal
  • Carcinoma, Neuroendocrine
  • Carcinoma, Thymic
  • Carcinoma, Pancreatic
  • Carcinoma Breast
  • Carcinoma, Ovarian
  • Carcinoma Bladder
  • Carcinoma of Unknown Primary
  • Carcinoma of the Head and Neck
  • Carcinoma of the Oropharynx
  • Carcinoma of the Larynx
  • Carcinoma of the Bladder
  • Carcinoma of Esophagus
  • Carcinoma of the Nasopharynx
  • Carcinoma of the Penis
  • Carcinoma of the Cervix
  • Carcinoma of the Anus
  • Carcinoma of the Vulva
  • Carcinoma of the Appendix
  • Carcinoma of the Oral Cavity
  • Cholangiocarcinoma
  • Melanoma
  • Mesothelioma
  • Pancreatic Cancer

Sponsors & Collaborators

  • xCures

    collaborator INDUSTRY
  • Travera Inc

    lead INDUSTRY

Principal Investigators

  • Mark Stevens, Phd · Travera Inc

  • Rob Kimmerling, Phd · Travera Inc

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-15
Primary Completion
2026-03-23
Completion
2026-03-23

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05461430 on ClinicalTrials.gov