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NCT03884400 Clinical Trial

Distribution of Biospecimens From Biorepositories/Biobanks for Research Use

Healthy Clinical Trial

Official title:
iSpecimen Network Distribution of Biospecimens From Biorepositories/Biobanks for Research Use

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT03884400
Other study ID # ISPC-180828-DISTRIBUTION
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date March 1, 2026

Study information
Verified date November 2022
Source iSpecimen Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This protocol seeks to assist biorepositories/biobanks in distributing their stored specimens and data to researchers that will actually utilize them to advance medicine and technology.

Description:

iSpecimen has built a partner network comprised of supplying institutions that have ethically acquired human biospecimens and created biorepositories/biobanks to store the specimens and data. Many of these biorepositories have protocols allowing for the collection of their samples but require an additional IRB or ethics review for the distribution of their samples. This protocol establishes a method of such supply sites to allow their specimens to be distributed and used for research via iSpecimen's technology and network of research clients.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date March 1, 2026
Est. primary completion date December 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Specimens and/or data from Biorepositories that have enrolled subjects that have provided consent for the specimens and de-identified data to be collected, stored and distributed. - Specimens from biobanks that have collected materials and de-identified data under a waiver of consent - Specimens from a biobank that meet the criteria for non human subject research under the common rule. Exclusion Criteria: - Specimens and/or that have been obtained from subjects without informed consent, nor waiver of consent or that do not meet the criteria for non human subject research under the common rule.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Specimens obtained from surgical, phlebotomy or other non-invasive procedure
Biospecimen Collection

Locations
Country Name City State
United States iSpecimen Lexington Massachusetts

Sponsors (1)
Lead Sponsor Collaborator
iSpecimen Inc

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Distribution of Biospecimens From Biorepositories/Biobanks for Research Use The number of specimens and subjects distributed per disease will be measured and reported. 15 years
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