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Autologous Peripheral Blood Stem Cell Transplantation With In Vivo Purging as an Alternate Stem Cell Transplantation Program for Pts w/AML in 1st & 2nd Complete Remission w/no HLA Matched Related Donor
This study has been completed.
Sponsor:
King Faisal Specialist Hospital & Research Center
Information provided by (Responsible Party):
King Faisal Specialist Hospital & Research Center
ClinicalTrials.gov Identifier:
NCT00531583
First received: September 17, 2007
Last updated: January 4, 2016
Last verified: January 2016
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Purpose
Autologous peripheral Bld Stem Cell Transplantation with In Vivo Purging as an alternate stem cell transplantation program for pts w/AML in 1st & 2nd complete remission w/no HLA matched related donor
| Condition | Intervention |
|---|---|
| Leukemia, Monocytic, Acute | Drug: Autologous peripheral Bld Stem Cell Transplantation with In Vivo Purging as an alternate stem cell transplantation |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Autologous Peripheral Blood Stem Cell Transplantation With In Vivo Purging as an Alternate Stem Cell Transplantation Program for Pts w/AML in 1st & 2nd Complete Remission w/no HLA Matched Related Donor |
Further study details as provided by King Faisal Specialist Hospital & Research Center:
Primary Outcome Measures:
- Efficacy [ Time Frame: 2009-2015 ]
| Enrollment: | 350 |
| Study Start Date: | March 2001 |
| Study Completion Date: | June 2015 |
| Primary Completion Date: | June 2015 (Final data collection date for primary outcome measure) |
Intervention Details:
-
Drug: Autologous peripheral Bld Stem Cell Transplantation with In Vivo Purging as an alternate stem cell transplantation
Autologous PBSCT
Eligibility| Ages Eligible for Study: | 18 Years to 85 Years (Adult, Senior) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patients with AML in 1st & 2nd complete remission w/no HLA matched related donor
Contacts and Locations
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To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00531583
Please refer to this study by its ClinicalTrials.gov identifier: NCT00531583
Locations
| Saudi Arabia | |
| KFSH&RC | |
| Riyadh, Saudi Arabia, 1211 | |
Sponsors and Collaborators
King Faisal Specialist Hospital & Research Center
Investigators
| Principal Investigator: | Fahad AlMohareb | KFSH&RC |
More Information
| Responsible Party: | King Faisal Specialist Hospital & Research Center |
| ClinicalTrials.gov Identifier: | NCT00531583 History of Changes |
| Other Study ID Numbers: |
RAC#2001-004 |
| Study First Received: | September 17, 2007 |
| Last Updated: | January 4, 2016 |
Keywords provided by King Faisal Specialist Hospital & Research Center:
|
AML in 1st & 2nd complete remission w/no HLA matched related donor |
Additional relevant MeSH terms:
|
Leukemia, Monocytic, Acute Leukemia, Myeloid, Acute Leukemia, Myeloid |
Leukemia Neoplasms by Histologic Type Neoplasms |
ClinicalTrials.gov processed this record on July 24, 2017