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NCT Number: NCT03869814

Non-invasive Liquid Biopsy Analysis of Epigenomics Signatures in Multiple Cancer Types

ClearNote Health is developing a test from whole blood for the early detection of multiple cancers. The goal of this study is to employ genomics, epigenomics and proteomics methodology for the detection of cancer signal in the blood of subjects with solid tumors.

Recruiting

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

ClearNote Health, Inc.

San Diego, California, 92121, United States

Location status: Recruiting

Location contact

Melissa Peters, MA, PMP, CCRC

CONTACT

[email protected]

833-258-7827

About this study

Epigenomic changes in cancer cells can provide a rich source of biomarker signals for the detection of disease. As cancer cells manifest their epigenomic changes in blood due to cell death, DNA and protein molecules can be probed using specific molecular analytic approaches. ClearNote Health employs epigenomic technologies to measure dynamic changes in DNA demethylation events via direct measurement of 5-hydroxymethyl-cytosine residues in cfDNA. Companion assays are also run to provide information on cfDNA digestion patterns and protein-based changes in plasma. This information, combined in a machine learning framework, enable the provision of prediction models that report on the presence of cancer and the determination of the tissue of tumor origin. This study will build predictive models and test performance of these models to detect the presence of cancer and tissue of origin in several cancer type by using a matched case-control study design.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects must be between 21-80 years of age at the time of enrollment
  • Patient fully consented
  • Cancer diagnosis OR high clinical suspicion for cancer, based on the participating site's and practitioner's standards of care (SOC)
  • No previous history of cancer and treatment naïve at time of enrollment

Exclusion criteria

  • Age < 21 OR > 80 years of age
  • Any prior cancer diagnosis with or without treatment (with the exception of non-melanoma skin cancers resolved/treated > 1 year prior to enrollment)
  • Receipt of any cancer therapy including chemotherapy, radiation, palliative radiation, hormonal or naturopathic therapies
  • In situ carcinoma without an invasive component
  • Any surgery requiring general anesthesia within 2 months of collection. Anesthesia used in procedures such as colonoscopy and EBUS is acceptable.
  • Receipt of systemic immunomodulation therapy within past 12 months
  • Currently pregnant, or pregnancy within last 12 months
  • Organ transplantation
  • Received dialysis
  • Blood transfusion within 1 month
  • Known HIV/AIDs, Hepatitis A, D, or E, TB, any kind of prion disorder (e.g., CJD) or other infectious pathogens currently present or present in past 5 years.

Treatment and study plan

Blood Draw

Other

Blood Draw

Primary outcomes

  1. Detection of cancer signal in the cancer cohort

    Time frame: Baseline

    Evaluation of genomics, proteomic and epigenomics signals, such as 5-hydroxymethylcytosine (5hmC), contained in plasma, in comparison to these signals in plasma from non-cancer controls

  2. Detection of tissue of origin signal in the cancer cohort

    Time frame: Baseline

    Evaluation of genomics, proteomic and epigenomics signals, such as 5-hydroxymethylcytosine (5hmC), contained in plasma, in comparison to these signals from non-cancer controls

Study contacts

Contact information is provided by the study sponsor or research team.

Melissa Peters, MA, PMP, CCRC

CONTACT

[email protected]

619-277-2160

Sponsors and collaborators

Lead sponsor

ClearNote Health

Industry

Registry information

Important dates

Study start
2018
Primary completion
2029
Study completion
2029
First posted
Mar 11, 2019
Registry last updated
May 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.