Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06222164

The Use of Residual De-identified Specimens and/or Samples From Patients for Clinical Research

Status
Recruiting
Phase
Study type
Observational
Enrollment
2,000 (estimated)
Sponsor
Invivoscribe, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Acquire residual human specimens and/or samples from patient samples which were sent for testing at LabPMM, LLC for Clinical Research

Detailed description

Residual specimen/sample collection study where peripheral blood (PB), bone marrow (BM), genomic (gDNA), and/or formalin-fixed paraffin-embedded tissue (FFPE) specimens/samples are obtained from patient samples sent to LabPMM, LLC for clinical testing. Samples may be used for Clinical Research at LabPMM, LLC or at partner institutions

Conditions

Timeline

Start date
2024-03-30
Primary completion
2027-03-30
Completion
2027-06-30
First posted
2024-01-24
Last updated
2025-05-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06222164. Inclusion in this directory is not an endorsement.

The Use of Residual De-identified Specimens and/or Samples From Patients for Clinical Research (NCT06222164) · Clinical Trials Directory