Mixed Chimeric Transplantation for Primary Amyloidosis

This study has been withdrawn prior to enrollment.
(Closed, never started.)
Information provided by:
Stanford University
ClinicalTrials.gov Identifier:
First received: September 13, 2005
Last updated: October 5, 2007
Last verified: October 2007
To evaluate the role of nonmyeloablative allogeneic transplantation in Amyloidosis.

Condition Intervention
Procedure: autologous followed by nonmyeloablative allogeneic transplant

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Mixed Chimeric Transplantation for Primary Amyloidosis

Resource links provided by NLM:

Further study details as provided by Stanford University:

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.

Estimated Enrollment: 45
Study Start Date: December 2000
Estimated Study Completion Date: September 2006

Ages Eligible for Study:   up to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • primary amyloidosis
  • adequate organ function
  • matched sibling donor

Exclusion Criteria:

  • evidence of multiple myeloma
  • HIV positive
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00186095

Sponsors and Collaborators
Stanford University
Principal Investigator: Keith Stockerl-Goldstein, MD Stanford University
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00186095     History of Changes
Other Study ID Numbers: BMT129 
Study First Received: September 13, 2005
Last Updated: October 5, 2007
Health Authority: United States: Institutional Review Board

Keywords provided by Stanford University:
cell transplantation

Additional relevant MeSH terms:
Metabolic Diseases
Proteostasis Deficiencies

ClinicalTrials.gov processed this record on February 10, 2016