Circulating Tumor DNA (ctDNA) for Early Treatment Response Assessment of Solid Tumors

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWashington University School of Medicine

About this trial

Earlier detection of disease recurrence will enable greater treatment options and has strong potential to improve patient outcomes. This project is translational and has the potential to lead to future translational research opportunities, including interventional trials in which therapeutic escalation is offered at the early circulating tumor DNA (ctDNA) molecular residual disease (MRD) detection timepoint. Ultimately, the integration of ctDNA into the clinical workflow has the potential to enhance cancer diagnosis, treatment, surveillance, and prognosis, and guide clinical decision-making in this era of personalized precision medicine.

Eligibility criteria

Qualifiers

Eligible healthy donors will be at least 18 years of age.

Disqualifiers

Healthy donors younger than 18 years of age

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

100 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Washington University School of Medicine

Lead sponsor

Roche Sequencing Solutions

Collaborator

The Foundation for Barnes-Jewish Hospital

Collaborator

National Center for Advancing Translational Sciences (NCATS)

Collaborator

Radiological Society of North America

Collaborator

Skandalaris

Collaborator

The V Foundation for Cancer Research

Collaborator

National Institute of General Medical Sciences (NIGMS)

Collaborator