"Castlebank": Castleman Disease Collaborative Network Biobank

Sponsor
Castleman Disease Collaborative Network (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02871050
Collaborator
(none)
0
1
24
0

Study Details

Study Description

Brief Summary

The purpose of this study is to create a biobank, which collects, stores, and distributes samples of human tissues, blood, and related health information to qualified scientists, in order to help doctors and researchers better understand why Castleman Disease occurs and develop ways to better treat and prevent it.

Detailed Description

The CDCN proposes to establish a biobank and associated clinical data for Castleman disease. Tissue and fluid (blood and saliva) samples will be collected both prospectively and retrospectively. Blood or saliva samples may also be collected from relatives of Castleman patients. Because of the scarcity of these samples, it will be necessary to make efforts to access all available cases. Many cases will occur at hospitals that do not have an existing relationship with the CDCN and may not have experience with tissue procurement; however, this is the only way to obtain the vast majority of samples. Samples may be used immediately, banked for future use, or further processed into DNA, cell lines, tissue microarrays, etc.

The samples will be stored at Precision for Medicine, a biorepository company that specializes in collection, processing, storage and distribution of biospecimens. Only researchers (US or international) who have applied to the CDCN and have been approved by the Biobank Advisory Board will be eligible to access biospecimens and/or data. The Biobank Advisory Board will be comprised of clinicians and scientists with experience in clinical and investigational practices in Castleman Disease.

Study Design

Study Type:
Observational
Actual Enrollment :
0 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
The Castleman Disease Collaborative Network Biobank: A Collection of Biospecimens and Clinical Data to Facilitate Research
Study Start Date :
Jun 1, 2016
Actual Primary Completion Date :
Jun 1, 2018
Actual Study Completion Date :
Jun 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Castleman Disease Patients

Potential study participants may be of any age, gender, or ethnicity who have been diagnosed with Castleman disease.

Other: Sample Collection
Excess blood sample tubes and/or buccal swabs or saliva will have DNA and RNA extracted and serum and plasma separated out to be stored for future research purposes based on the results of this preliminary research.

Outcome Measures

Primary Outcome Measures

  1. Samples Collected [3 years]

    Number of samples collected across different subgroups (e.g. blood products, lymph node)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

  • Potential study participants may be of any age, gender, or ethnicity who have been diagnosed with Castleman disease

Exclusion Criteria

  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Castleman Disease Collaborative Network Philadelphia Pennsylvania United States 19146

Sponsors and Collaborators

  • Castleman Disease Collaborative Network

Investigators

  • Principal Investigator: David C Fajgenbaum, MD, MBA, MSc, Executive Director of Castleman Disease Collaborative Network

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Castleman Disease Collaborative Network
ClinicalTrials.gov Identifier:
NCT02871050
Other Study ID Numbers:
  • #31132/1
First Posted:
Aug 18, 2016
Last Update Posted:
Jul 31, 2018
Last Verified:
Jul 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Keywords provided by Castleman Disease Collaborative Network
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 31, 2018