Compliant Analysis of Patient Samples and Data
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorSequenom, Inc.
About this trial
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.
Eligibility criteria
Qualifiers
Arm 1
All samples and data are de-identified and HIPAA compliant
Arm 2
Subject is of scientific interest to the Sponsor or treating physician
Disqualifiers
Arm 1
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
Arm 2
Any medical or mental condition that would interfere with the subjects' ability to willingly give written informed consent
Trial design
Treatments tested in this trial
- Multiple interventions depending on diagnostic test being run.
Treatment groups
No treatment groups listed
Sponsors and collaborators
Sequenom, Inc.
Lead sponsor
Laboratory Corporation of America
Collaborator
Source ClinicalTrials.gov