[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

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Adenoma,Colon Cancer,Rectal Diseases,Colon Diseases,Colon Lesion,Colon Neoplasm,Colon Polyp,Colorectal Cancer,Gastrointestinal Tract Cancers,Polyp,Rectal Cancer

Treatment type


Investigational product

Freenome test


Freenome, Inc.

ClinicalTrials.gov identifier


Study number


Understanding clinical trials

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About the study

The PREEMPT CRC study is a prospective multi-center observational study to validate a blood-based test for the early detection of colorectal cancer by collecting blood samples from average-risk participants who will undergo a routine screening colonoscopy.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria
Exclusion criteria
  1. HNPCC) or Lynch syndrome, or familial adenomatous polyposis (
  2. FAP) 2. Personal history 2.1 CRC or colorectal adenoma 2.2 Inflammatory bowel disease (IBD), including chronic ulcerative colitis (
  3. CUC) and crohn's disease (
  4. CD) 2.3 Colonoscopy in the 9 years preceding enrollment 2.4 Stool DNA testing in the 2 years preceding enrollment 2.5 Symptoms of lower gastrointestinal tract disease warranting colonoscopic evaluation 3. A medical condition which, in the opinion of the Investigator, should preclude enrollment in the study 4. Participated or currently participating in a clinical research study in which an experimental medication has been administered during the 60 days up to and including the date of providing informed consent or may be administered through the time of the colonoscopy

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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