RECRUITING

Compliant Analysis of Patient Samples and Data

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

Patients of scientific interest who have provided a commercial sample to LabCorp or one of its' affiliates will have their de-identified remnant samples and/or data used for research and development. Other commercial patients will be followed up on after informed consent is obtained.

Official Title

Use of Patient Samples and Corresponding Clinical Data for Research and Development Studies And/or Population-based Analysis

Quick Facts

Study Start:2018-03-17
Study Completion:2030-08-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04364503

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. * Arm 1
  2. * All samples and data are de-identified and HIPAA compliant
  3. * Arm 2
  4. * Subject is of scientific interest to the Sponsor or treating physician
  5. * Subject provides written informed consent and has a clinical sample and/or supporting clinical data collected.
  1. * Arm 1
  2. * Subject is from a US state or a country where local law restricts the use of de-identified data and/or remnants of specimens for research and/or development
  3. * Arm 2
  4. * Any medical or mental condition that would interfere with the subjects' ability to willingly give written informed consent

Contacts and Locations

Study Contact

Graham P Senior Director
CONTACT
(858) 202-2000
mclenng@labcorp.com

Principal Investigator

Graham P McLennan
PRINCIPAL_INVESTIGATOR
Sequenom, Inc.

Study Locations (Sites)

Sequenom, Inc
San Diego, California, 92121
United States

Collaborators and Investigators

Sponsor: Sequenom, Inc.

  • Graham P McLennan, PRINCIPAL_INVESTIGATOR, Sequenom, Inc.

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 Date2018-03-17
Study Completion Date2030-08-15

Study Record Updates

Study Start Date2018-03-17
Study Completion Date2030-08-15

Terms related to this study

Additional Relevant MeSH Terms

  • Pregnancy Related
  • Cancer
  • Infectious Disease