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NCT Number: NCT05673018

Galleri® in the Medicare Population.

This multi-center comparative prospective cohort study is designed to assess the real world clinical impact, including safety and test performance, of Galleri®, a blood-based multi-cancer early detection (MCED) test. The study will seek enrollment that is representative of the Medicare population.

Recruiting

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Key information

Conditions

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mercy Health - Fort Smith, Fort Smith, Arkansas, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

For Galleri + UC (Galleri-Tested Arm):

Participants are eligible to be included in the study only if all of the following criteria apply:

  • Aged ≥50 years with Medicare coverage, including Traditional Medicare (Part A & B or Dual Eligibles) or Medicare Advantage.
  • Capable of giving informed consent that is legally effective (consent provided by a legally authorized representative is not permitted in this protocol).

For UC (Not Galleri-tested Arm):

Participants are eligible to be included in the study only if all of the following criteria apply:

  • Aged ≥ 50 years with Medicare coverage, including Traditional Medicare (Part A & B or Dual Eligibles) or Medicare Advantage.
  • Have had ≥ 1 UC visit

Exclusion criteria

For Galleri + UC (Galleri-Tested Arm):

  • Evidence of having had a previous MCED test (including but not limited to the Galleri test, e.g. CancerSeek, PanSeer). Participation in a study such as GRAIL's STRIVE study where results were not returned is not an exclusion criterion.
  • Undergoing clinical evaluation for suspicion of cancer within 6 months prior to enrollment. Personal history of hematologic malignancy and/or invasive solid tumor (excluding non-metastatic basal cell carcinoma and squamous cell carcinoma of the skin):
  • Diagnosed ≤3 years before expected enrollment date and/or
  • Diagnosed >3 years before expected enrollment date and never treated and/or
  • Currently undergoing active cancer management (not including adjuvant hormone therapy for breast or prostate cancer).
  • Current pregnancy.
  • Individuals who are currently inpatients at a participating site.
  • Individuals who are not willing or able to comply with the protocol procedures.
  • Individuals who are not currently registered patients at a participating center.
  • Previous or current employees or contractors of GRAIL.

For UC (Not Galleri-tested Arm):

  • Evidence of having had a previous MCED test (including but not limited to the Galleri test, eg.CancerSeek, PanSeer). Participation in a study such as GRAIL's STRIVE study where results were not returned is not an exclusion criterion.
  • Undergoing clinical evaluation for suspicion of cancer.
  • Personal history of hematologic malignancy and/or invasive solid tumor (not including non-metastatic basal cell carcinoma and squamous cell carcinoma of the skin):
  • Diagnosed ≤3 years before expected enrollment date and/or
  • Diagnosed >3 years before expected enrollment date and never treated and/or
  • Currently undergoing active cancer management (not including adjuvant hormone therapy for breast or prostate cancer).
  • Current pregnancy.
  • Individuals who are currently inpatients at a participating site.

Treatment and study plan

Multi-Cancer Early Detection Test (Galleri®)

Device

Blood collection and multi-cancer early detection testing with return of results.

Primary outcomes

  1. Incidence rates of stage IV cancers

    Time frame: Up to 3 Years

Secondary outcomes

  1. Safety: Number and type of invasive procedures performed to evaluate a cancer signal detected test result

    Time frame: Up to 3 Years

  2. Galleri test performance in the Galleri + UC arm

    Time frame: Up to 3 Years

  3. Adherence to guideline-recommended cancer screening in the Galleri+UC arm and UC arm over time

    Time frame: Up to 3 Years

  4. Healthcare resource utilization associated with cancer diagnostic evaluations in the Galleri+UC arm and UC arm

    Time frame: Up to 3 Years

Study contacts

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

GRAIL Medical Information

CONTACT

[email protected]

833-694-2553

Sponsors and collaborators

Lead sponsor

GRAIL, Inc.

Industry

Registry information

Official study title

REACH Study: Galleri® in the Medicare Population.

Important dates

Study start
2024
Primary completion
2030
Study completion
2030
First posted
Jan 5, 2023
Registry last updated
May 22, 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.

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