Distribution of Biospecimens From Biorepositories/Biobanks for Research Use

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2021-01-01

Study Completion Date

2026-03-01

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Cancer Pregnancy Related Gastro-Intestinal Disorder Cardio-Respiratory Distress Women's Health: Endometriosis Autoimmune Diseases Nephritis Healthy Neuro-Degenerative Disease

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Subjects who have provided consent for specimen collection

Re-consent will not be required. This protocol allows distribution of the specimens following the terms agreed to by the subject in the original consent.

Specimens obtained from surgical, phlebotomy or other non-invasive procedure

Intervention Type PROCEDURE

Biospecimen Collection

Interventions

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Specimens obtained from surgical, phlebotomy or other non-invasive procedure

Biospecimen Collection

Intervention Type PROCEDURE

Eligibility Criteria

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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.

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes