Actively Recruiting
Compliant Analysis of Patient Samples and Data
Led by Sequenom, Inc. · Updated on 2024-10-16
2000
Participants Needed
1
Research Sites
647 weeks
Total Duration
On this page
Sponsors
S
Sequenom, Inc.
Lead Sponsor
L
Laboratory Corporation of America
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Compliant Analysis of Patient Samples and Data
Who Can Participate
Eligibility Criteria
You may qualify if you...
- For Arm 1: All samples and data are de-identified and compliant with HIPAA
- For Arm 2: Subject is of scientific interest to the Sponsor or treating physician
- For Arm 2: Subject provides written informed consent and has a clinical sample and/or supporting clinical data collected
You will not qualify if you...
- For Arm 1: Subject is from a US state or country where local law restricts use of de-identified data or specimen remnants for research or development
- For Arm 2: Any medical or mental condition interfering with the subject's ability to willingly give written informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sequenom, Inc
San Diego, California, United States, 92121
Actively Recruiting
Research Team
G
Graham P Senior Director
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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