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NCT04396808Active, not recruiting

Genomics in Michigan to AdJust Outcomes in Prostate canceR (G-MAJOR) for Men With Newly Diagnosed Favorable Risk Prostate Cancer

Genomics in Michigan to AdJust Outcomes in Prostate canceR (G-MAJOR): A Randomized Multi-center Study for Men With Newly Diagnosed Favorable Risk Prostate Cancer

Source: ClinicalTrials.gov · Last updated 9 Sept 2026

Brief summary (registry, in English)

This study seeks to determine the clinical impact of Gene Expression Classifier (GEC) testing in prostate cancer care while also developing a pragmatic approach for improved GEC clinical use and future study.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
805 (actual)
First submitted
15 May 2020
Start date
5 Nov 2020
Primary completion date
31 Mar 2028
Lead sponsor
University of Michigan Rogel Cancer Center
NCT number
NCT04396808

What you commit to

  • Study type: Interventional
  • Participants enrolled: 805
  • From 5 Nov 2020 to the primary completion date, 31 Mar 2028
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior prostate cancer treatment, including prostatectomy, radiation therapy, or hormone therapy.
  • Prior prostate gene expression classier testing

Other illness

  • Clinical (on digital rectal exam) or radiographic evidence (if MRI performed) of T3 disease
  • Nodal or metastatic prostate cancer (if staging imaging performed)

Who the study is looking for

  • Prostate cancer patients who have undergone diagnostic prostate biopsy in the past 9 months.
  • Prostate biopsy tumor tissue (FFPR block) available for processing
  • Age 18 years or older
  • PSA \<20 ng/ml
  • Grade Group (GG) 1 cancer with \> 2 biopsy cores involved with cancer OR GG2 cancer
  • Ability to understand and the willingness to sign a written informed consent. A subject's legally acceptable representative may sign the consent form.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Michigan Rogel Cancer Center
Coordinator of this site? Confirm its status
Ann ArborUnited StatesUnknown status
University of North Carolina
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status
Sherwood Medical Center
Coordinator of this site? Confirm its status
DetroitUnited StatesUnknown status
Henry Ford Health System
Coordinator of this site? Confirm its status
DetroitUnited StatesUnknown status
Spectrum Health Medical Group
Coordinator of this site? Confirm its status
Grand RapidsUnited StatesUnknown status
Western Michigan Urological Associates
Coordinator of this site? Confirm its status
HollandUnited StatesUnknown status
University of Pennsylvania Perelman School of Medicine
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Montefiore Medical Center
Coordinator of this site? Confirm its status
The BronxUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.