RECRUITING

The TIOB - Collection of Patients' Biospecimens for Analysis of Immunological and Molecular Biomarkers.

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of the Texas Immuno-Oncology Biorepository (TIOB) is to collect and store well-defined and well-annotated serial biospecimens of tissue, blood, urine and stool in a longitudinal manner from cancer patients who are receiving either standard of care surgical interventions and or FDA approved immunotherapeutics across the largest not-for-profit health system in Texas. Comprehensive clinical and radiological data from a diverse population of patients with different racial, social and ethnic backgrounds matched with serial biospecimens over a patients journey with cancer marks the TIOB as a unique research facility.

Official Title

The Texas Immuno-Oncology Biorepository: Collection of Patients' Biospecimens for Analysis of Immunological and Molecular Biomarkers That Predict Benefit/Resistance to Cancer Therapeutics.

Quick Facts

Study Start:2020-09-11
Study Completion:2052-09-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05371756

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Understand and willingness to sign written informed consent method.
  2. * Patients who are suspected by a physician of being at risk for developing cancer.
  3. * Patients with confirmed or clinically suspected malignancy by a physician. This includes but is not limited to candidates for immunotherapy, surgical candidates, patients receiving Standard of Care drugs, immunotherapy drugs, participating on a clinical trial with immunotherapy drugs, patients who have received immunotherapy drugs in the past, patients with any other approved or investigational disease management.
  1. * Patients unwilling to donate blood
  2. * Patients unwilling to provide informed consent for the collection of fresh or archived tumor tissue.

Contacts and Locations

Study Contact

Sido Oghenevovwero, MS
CONTACT
214-820-6168
corcsolidtumor@BSWHealth.org
Keisha Riser, MBA
CONTACT
214-820-8165
keisha.riser@bswhealth.org

Principal Investigator

Ronan Kelly, MD
PRINCIPAL_INVESTIGATOR
Baylor Scott & White Research Institute

Study Locations (Sites)

Baylor Scott & White Research Institute
Dallas, Texas, 75246
United States

Collaborators and Investigators

Sponsor: Baylor Research Institute

  • Ronan Kelly, MD, PRINCIPAL_INVESTIGATOR, Baylor Scott & White Research Institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-09-11
Study Completion Date2052-09-11

Study Record Updates

Study Start Date2020-09-11
Study Completion Date2052-09-11

Terms related to this study

Keywords Provided by Researchers

  • Biorepository
  • Immuno-Oncology
  • Molecular Biomarkers
  • Benefit & Resistance

Additional Relevant MeSH Terms

  • Cancer