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Trial · NCT00579111

Reduced Intensity Preparative Regimen Followed by Stem Cell Transplant (FAB)

NCT00579111, Phase 1, Phase 2, Terminated, Baylor College of Medicine; results first posted 2012-08-09

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Reduced Intensity Preparative Regimen Followed by Stem Cell Transplant (FAB). Trials, record NCT00579111. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00579111

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Reduced Intensity Preparative Regimen Followed by Stem Cell Transplant (FAB)
NCT number
NCT00579111
Status
Terminated
Phases
Phase 1, Phase 2
Enrollment
4 participants, actual
Lead sponsor
Baylor College of Medicine
Conditions
Myelodysplastic and Myeloproliferative Disorders, Acute Myelogenous Leukemia, Acute Lymphoblastic Leukemia, Chronic Myelogenous Leukemia, Multiple Myeloma, Plasma Cell Dyscrasia, Lymphoproliferative Disorders, Hematologic Diseases
Interventions
Campath, Busulfan, Fludarabine, Hematopoietic stem cell infusion, FK-506
First posted
2007-12-21
Last updated
2016-05-04
Results first posted
2012-08-09

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of Patients With Successful Donor Engraftment100 daysEach patient will be classified as a success or failure. A success will be defined as engraftment of at least 35% of cells 100 days after transplant.
SecondaryNumber of Patients With Treatment Related Grade III or IV Non-hematological Toxicity100 days

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Patients With Successful Donor Engraftment100 daysparticipantsNUMBER
SECONDARYNumber of Patients With Treatment Related Grade III or IV Non-hematological Toxicity100 daysparticipantsNUMBER

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Patients With Successful Donor EngraftmentHLA-identical Sibling Transplant2participants
Number of Patients With Successful Donor EngraftmentUnrelated Matched or Single Antigen Mismatched Transplant1participants
Number of Patients With Treatment Related Grade III or IV Non-hematological ToxicityHLA-identical Sibling Transplant1participants
Number of Patients With Treatment Related Grade III or IV Non-hematological ToxicityUnrelated Matched or Single Antigen Mismatched Transplant0participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDHLA-identical Sibling Transplant3
Overall StudySTARTEDUnrelated Matched or Single Antigen Mismatched Transplant1
Overall StudyCOMPLETEDHLA-identical Sibling Transplant1
Overall StudyCOMPLETEDUnrelated Matched or Single Antigen Mismatched Transplant0
Overall StudyNOT COMPLETEDHLA-identical Sibling Transplant2
Overall StudyNOT COMPLETEDUnrelated Matched or Single Antigen Mismatched Transplant1

Adverse events4

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousBlood/Bone Marrow - Other: Engraftment FailureBlood and lymphatic system disordersHLA-identical Sibling Transplant131
seriousBlood/Bone Marrow - Other: Engraftment FailureBlood and lymphatic system disordersUnrelated Matched or Single Antigen Mismatched Transplant010
seriousInfection (documented clinically or microbiologically) with Grade 3 or 4 neutrophils (ANC <1.0 x 10eInfections and infestationsHLA-identical Sibling Transplant132
seriousInfection (documented clinically or microbiologically) with Grade 3 or 4 neutrophils (ANC <1.0 x 10eInfections and infestationsUnrelated Matched or Single Antigen Mismatched Transplant010

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityHLA-identical Sibling Transplant
Total, all-cause mortalityUnrelated Matched or Single Antigen Mismatched Transplant
Total, other adverse eventsHLA-identical Sibling Transplant03
Total, other adverse eventsUnrelated Matched or Single Antigen Mismatched Transplant01
Total, serious adverse eventsHLA-identical Sibling Transplant23
Total, serious adverse eventsUnrelated Matched or Single Antigen Mismatched Transplant01

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons3

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
HLA-identical Sibling Transplant vs Unrelated Matched or Single Antigen Mismatched Transplant: Number of Patients With Successful Donor EngraftmentTrial comparisons
HLA-identical Sibling Transplant vs Unrelated Matched or Single Antigen Mismatched Transplant: Number of Patients With Treatment Related Grade III or IV Non-hematological ToxicityTrial comparisons
HLA-identical Sibling Transplant vs Unrelated Matched or Single Antigen Mismatched Transplant: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00579111

GET https://conductscience.org/api/trials/v1/NCT00579111/registered