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  • Phase 2 Study To Evaluate The Efficacy And Safety Of TPST-1495 In Patients With Familial Adenomatous Polyposis (FAP) Scottsdale/Phoenix, Ariz., Rochester, Minn.

    This open-label phase II trial tests how well TPST-1495 works in reducing the number of polyps in the small bowel and colon in patients with familial adenomatous polyposis (FAP). FAP is an inherited condition in which numerous polyps (growths that protrude from mucous membranes) form on the inside walls of the colon and rectum. It increases the risk for colon cancer. TPST-1495 binds to specific prostaglandin receptors. TPST-1495 is a dual antagonist of the prostaglandin E2 (PGE2) receptor subtypes EP2 and EP4, while sparing the immune-stimulating EP1 and EP3 receptors. TPST-1495 may help reduce the number of polyps in the small bowel and colon in patients with FAP.

Closed for Enrollment

  • A Biobank for Pancreatic Diseases Rochester, Minn.

    To develop a resource (bank) of biospecimens and data collected from individuals with pancreatic diseases to facilitate discovery and development of novel biomarkers of risk and early detection, severity prediction, etiology and response to therapy.

     

  • A Phase IIB Clinical Trial of the Multitargeted Recombinant Adenovirus 5 (CEA/MUC1/Brachyury) Vaccine (TRI-AD5) and IL-15 Superagonist N-803 in Lynch Syndrome Rochester, Minn., Scottsdale/Phoenix, Ariz.

    The purpose of this study is to evaluate if the combination of trivalent adenovirus-5 (Tri-Ad5) vaccines and IL-15 superagonist N-803 reduces the incidence of colorectal neoplasms in patients with Lynch syndrome (LS).

  • Automating Colonoscopy Follow-up to Facilitate Appropriate Colonoscopy Surveillance Rochester, Minn.

    The primary goals of this project will be to standardize and enhance recommendations for colonoscopy surveillance intervals across the divisions of GIH and CRS and throughout the clinic practice

  • CPN1741 T-Cell Receptor Repertoire (TCR) Repertoire Pre- and Post-MUC1 Vaccine Rochester, Minn. Can T cell receptor repertoires serve as a biomarker of T cell response to a MUC1 vaccine?
  • Genomic analyses of pancreatic or hepatobilliary tumors Jacksonville, Fla., Scottsdale/Phoenix, Ariz., Rochester, Minn. This study is designed to identify mutational signatures in cancers arising in patients enrolled in the IRBs 18-000326 and 18-00275. Specifically we will apply advanced genomic analyses including whole genome sequencing, to the tumors arising in patients enrolled in the IRBs 18-000326 and 18-00275. This study, although largely exploratory, aims to better understand genomic changes in cancers arising in patients with germ line variants in genes associated with cancer risk, and evaluate their clinical implications.
  • Mayo Center for Cell Signaling Biobank (C-SiG Biobank) Rochester, Minn.

    The purpose of this study is to facilitate discovery and development of novel biomarkers of risk and early detection, etiologic factors relating to liver disease, and novel targeted therapeutic and chemopreventive strategies for liver disease such as PSC, PBC, PLD, NAFLD, NASH, ASH, HCC, donors (non-diseased and diseased) for liver transplant or non-liver diseased subjects scheduled for surgery will serve as controls.

  • Mayo Clinic Cancer Genomics Service Line Biorepository Rochester, Minn., Eau Claire, Wis., Scottsdale/Phoenix, Ariz., Jacksonville, Fla.

    The goal of the study is to create a database of clinical information and a repository of biological specimens for genetic, molecular and microbiological research to better understand hereditary cancer and help develop new therapies and preventive strategies.

  • Randomized, Double-Blind, Placebo-Controlled Trial of MUC1 Vaccine in Patients With Newly Diagnosed Advanced Adenomas Rochester, Minn. This randomized phase II clinical trial studies how well MUC1 peptide-poly-ICLC adjuvant vaccine works in treating patients with newly diagnosed advanced colon polyps (adenomatous polyps). Adenomatous polyps are growths in the colon that may develop into colorectal cancer overtime. Vaccines made from peptides may help the body build an effective immune response to kill polyp cells. MUC1 peptide-poly-ICLC adjuvant vaccine may also prevent the recurrence of adenomatous polyps and may prevent the development of colorectal cancer.
  • The Circulating Cell-free Genome Atlas Study (CCGA) Rochester, Minn., Jacksonville, Fla., Scottsdale/Phoenix, Ariz.

    GRAIL is using deep sequencing of circulating cell-free nucleic acids (cfNAs) to develop assays to detect cancer early in blood. The purpose of this study is to collect biological samples from donors with a new diagnosis of cancer (blood and tumor tissue) and from donors who do not have a diagnosis of cancer (blood) in order to characterize the population heterogeneity in cancer and non-cancer subjects and to develop models for distinguishing cancer from non-cancer.

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