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RecruitingNCT06222164Updated May 4, 2025

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

An observational study in Hematologic Diseases, sponsored by Invivoscribe, Inc.. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-05-04.

Sponsored by Invivoscribe, Inc. · Observational

From the registry’s dates

  • Started Mar 2024; still recruiting 2 years 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Ages
18 Years and older
Sex
All
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Study summary

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

Read the 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

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Conditions studied

  • Hematologic Diseases

Browse trials for

Keywords

  • residual samples hematologic diseases
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In context

Hematologic Diseases

460 studies on the registry are indexed under Hematologic Diseases; 105 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 228 across 129 observational studies indexed under Hematologic Diseases.

Browse Hematologic Diseases studies →

Lead sponsor

Invivoscribe, Inc. is the lead sponsor of 4 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Specimen/sample, peripheral blood (PB), bone marrow (BM), genomic DNA (gDNA) and/or formalin-fixed paraffin-embedded tissue (FFPE) from patients whose specimens/samples have been sent to LabPMM for clinical testing

Inclusion criteria

  1. Specimen/sample, peripheral blood (PB), bone marrow (BM), genomic DNA (gDNA) and/or formalin-fixed paraffin-embedded tissue (FFPE) from patients whose specimens/samples have been sent to LabPMM for clinical testing
  2. Donor Age ≥ 18 years

Exclusion criteria

Exclusion Criteria:

  1. Sample/specimen has been obtained from a third-party vendor with a Materials Transfer Agreement (MTA) on file with LabPMM
  2. The specimens/samples have previously been enrolled in a clinical study
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Residual Specimens

    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.

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What researchers measure

Primary outcomes

  1. Enrollment

    N=2000

    Time frame: 3 years

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Study locations

1 of 1 sites recruiting
  • LabPMM
    San Diego, California 92121, United States
    Recruiting
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References and documents

Related links

Individual participant data

Plan to share: Undecided — Study uses residual de-identified human samples

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06222164
Lead sponsor
Invivoscribe, Inc.
Responsible party
Sponsor
First posted
Jan 24, 2024
Start date
Mar 30, 2024
Primary completion
Mar 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
May 4, 2025

Study contacts

Andrew Schut
Contact
aschut@invivoscribe.com
+1 858.224.6600

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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