Recruiting

Observational Study

Sponsor:

Adela, Inc

Code:

NCT05366881

Conditions

Brain Cancer

Breast Cancer

Bladder Cancer

Cervical Cancer

Colorectal Cancer

Eligibility Criteria

Sex: All

Age: 40+

Healthy Volunteers: Accepted

Study Details

Brief summary:

This is an observational case-control study to train and validate a genome-wide methylome enrichment platform to detect multiple cancer types and to differentiate amongst cancer types. The cancers included in this study are brain, breast, bladder, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatobiliary, leukemia, lung, lymphoma, multiple myeloma, ovarian, pancreatic, prostate, renal, sarcoma, and thyroid. These cancers were selected based on their prevalence and mortality to maximize impact on clinical care.

Additionally, the ability of the whole-genome methylome enrichment platform to detect minimal residual disease after completion of cancer treatment and to detect relapse prior to clinical presentation will be evaluated in lung cancer. This cancer was selected based on the existing clinical landscape and treatment availability.

Conditions

Brain Cancer

Breast Cancer

Bladder Cancer

Cervical Cancer

Colorectal Cancer

Study ID

NCT05366881

Start date

May 3, 2022

Status verified date

Jan, 2026

Completion date

Mar, 2027

Anticipated

Primary completion date

Mar, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 40+

Healthy Volunteers: Accepted

Case Inclusion Criteria:

  • Newly diagnosed (within 120 days) with cancer or a recurrence of a cancer diagnosed >5 years ago of one of the following subtypes: Invasive Brain, Breast, Bladder, Cervical, Colorectal, Endometrial, Esophageal, Gastric, Head and Neck, Hepatobiliary, Lung, Ovarian, Pancreatic, Prostate, Renal, Sarcoma, Thyroid; Leukemia, Lymphoma, Multiple Myeloma
  • Able and willing to provide informed consent
  • ≥40 years of age

Case Exclusion Criteria:

  • Currently receiving any treatment for cancer
  • Currently taking any demethylating agents/DNA hypomethylating agents
  • Simultaneously diagnosed with two or more invasive cancers
  • Diagnosed with any invasive or non-invasive cancer in addition to the index cancer in the last 5 years
  • Currently diagnosed with any chronic hematopoietic cancer (e.g. chronic CLL) in addition to the index cancer
  • Currently diagnosed with any myelodysplastic syndromes and/or precursor hematologic conditions (e.g. MGUS) in addition to the index cancer
  • Women who are known to be pregnant (self-reported)

Control Inclusion Criteria

  • Not diagnosed with any cancer in the last 5 years (non-invasive cancer is allowed)
  • Able and willing to provide informed consent
  • ≥40 years of age

Control Exclusion Criteria

  • Currently receiving any treatment for cancer
  • Currently taking any demethylating agents/DNA hypomethylating agents
  • Women who are known to be pregnant (self-reported)

Study Design

Enrollment

7000 participants

Anticipated

Interventions and Outcome Measures

Arms

Cases

Cases will include participants with newly diagnosed, treatment-naive cancer at the time of enrollment.

Controls

Controls will include participants without known cancer at the time of enrollment.

Primary outcome measure

  • Detection of cancer [ Time Frame: 24 months ]

Central Contacts and Locations

Locations

City of Hope

Recruiting

Duarte, California, United States, 91010

Contacts

Principal Investigator:

Gregory Idos, MD

Miami Cancer Institute

Recruiting

Miami, Florida, United States, 33176

Contacts

Principal Investigator:

Manmeet Ahluwalia, MD

North Georgia Health System

Recruiting

Gainesville, Georgia, United States, 306501

Contacts

Principal Investigator:

Charles Nash, MD

Baptist Floyd

Recruiting

New Albany, Indiana, United States, 47150

Contacts

Principal Investigator:

Amitoj Gill, MD

Baptist Corbin

Recruiting

Corbin, Kentucky, United States, 40701

Contacts

Principal Investigator:

Abigail Byrnes, MD

Baptist Hardin

Recruiting

Elizabethtown, Kentucky, United States, 42701

Contacts

Principal Investigator:

Christopher Burkeen, MD

Baptist Lexington

Recruiting

Lexington, Kentucky, United States, 40503

Contacts

Principal Investigator:

Arvinda Padmanabhan, MD

Allina Health Cancer Institute

Recruiting

Minneapolis, Minnesota, United States, 55407

Contacts

Principal Investigator:

Joleen Hubbard, MD

Mayo Clinic

Recruiting

Rochester, Minnesota, United States, 55902

Contacts

Angela R Emanuel

emanuel.angela@mayo.edu

Principal Investigator:

Lisa A Boardman, MD

Cleveland Clinic

Recruiting

Cleveland, Ohio, United States, 44195

Contacts

Mofetoluwa Oluwasanmi

216-444-0843oluwasm@ccf.org

Principal Investigator:

Peter Mazzone, MD, MPH

Oregon Health Sciences University

Recruiting

Portland, Oregon, United States, 97201

Contacts

Diana Potts

pottsd@ohsu.edu

Principal Investigator:

Nima Nabavizadeh, MD

Medical University of South Carolina

Recruiting

Charleston, South Carolina, United States, 29425

Contacts

Principal Investigator:

Gerard Silvestri, MD

McLeod Health

Recruiting

Florence, South Carolina, United States, 29502

Contacts

Principal Investigator:

Virginia Clyburn-Ipock, MD

Baptist (BHMCC)

Recruiting

Memphis, Tennessee, United States, 38120

Contacts

Principal Investigator:

Philip Lammers, MD

Vanderbilt-Ingram Cancer Center

Recruiting

Nashville, Tennessee, United States, 37203

Contacts

Principal Investigator:

Brian Rini, MD

Elligo Health Research, Inc.

Recruiting

Austin, Texas, United States, 78704

Contacts

Principal Investigator:

Faith Holmes, MD

More Information

Sponsor

Adela, Inc

Last update posted

Jan 20, 2026

Last verified

Jan, 2026

Keywords

  • Multi-cancer early detection
  • Liquid Biopsy
  • Methylome
  • Cancer screening
  • cell-free DNA

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Adela, Inc on 2026-01-20.