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Compliant Analysis of Patient Samples and Data

Recruiting
years of age
Both
Phase N/A

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Overview

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.

Description

Arm 1 - Remnant commercial samples and data that has been de-identified of personal health information in compliance with HIPAA may be used for R&D studies or population-based analysis by LabCorp or affiliates.

Arm 2 - Collection of samples and/or data from commercial test patients requiring follow-up or from subjects of scientific interest after informed consent is obtained.

Eligibility

Inclusion Criteria:

  • 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
  • Subject provides written informed consent and has a clinical sample and/or supporting clinical data collected.

Exclusion Criteria:

  • 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

Study details

Pregnancy Related, Cancer, Infectious Disease

NCT04364503

Sequenom, Inc.

25 January 2024

Step 1 Get in touch with the nearest study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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