Mixed Chimeric Transplantation for Primary Amyloidosis
Primary Purpose
Amyloidosis
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
autologous followed by nonmyeloablative allogeneic transplant
Sponsored by
About this trial
This is an interventional treatment trial for Amyloidosis focused on measuring Amyloidosis, nonmyeloablative, hematopoietic, cell transplantation
Eligibility Criteria
Inclusion Criteria: primary amyloidosis adequate organ function matched sibling donor Exclusion Criteria: evidence of multiple myeloma HIV positive
Sites / Locations
Outcomes
Primary Outcome Measures
Treatment of patients with nonmyeloablative allogeneic transplant for amyloidosis.
Secondary Outcome Measures
Toxicity of therapy
Changes in marrow and serum abnormalities
Improvement in end-organ function.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00186095
Brief Title
Mixed Chimeric Transplantation for Primary Amyloidosis
Official Title
Mixed Chimeric Transplantation for Primary Amyloidosis
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Withdrawn
Why Stopped
Closed, never started.
Study Start Date
December 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Stanford University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To evaluate the role of nonmyeloablative allogeneic transplantation in Amyloidosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amyloidosis
Keywords
Amyloidosis, nonmyeloablative, hematopoietic, cell transplantation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
autologous followed by nonmyeloablative allogeneic transplant
Primary Outcome Measure Information:
Title
Treatment of patients with nonmyeloablative allogeneic transplant for amyloidosis.
Secondary Outcome Measure Information:
Title
Toxicity of therapy
Title
Changes in marrow and serum abnormalities
Title
Improvement in end-organ function.
10. Eligibility
Sex
All
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
primary amyloidosis
adequate organ function
matched sibling donor
Exclusion Criteria:
evidence of multiple myeloma
HIV positive
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keith Stockerl-Goldstein, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Mixed Chimeric Transplantation for Primary Amyloidosis
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