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Trial · NCT00587054

Trial of Allogeneic Stem Cell Transplants From HLA Compatible, Related and Unrelated Donors After a Myeloablative Preparative Regimen With Hyperfractionated TBI, Thiotepa and Fludarabine For Adult Patients With Lymphohematopoietic Disorders

NCT00587054, Phase 2, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2017-03-10

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Trial of Allogeneic Stem Cell Transplants From HLA Compatible, Related and Unrelated Donors After a Myeloablative Preparative Regimen With Hyperfractionated TBI, Thiotepa and Fludarabine For Adult Patients With Lymphohematopoietic Disorders. Trials, record NCT00587054. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00587054

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Trial

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

Title
Trial of Allogeneic Stem Cell Transplants From HLA Compatible, Related and Unrelated Donors After a Myeloablative Preparative Regimen With Hyperfractionated TBI, Thiotepa and Fludarabine For Adult Patients With Lymphohematopoietic Disorders
NCT number
NCT00587054
Status
Completed
Phases
Phase 2
Enrollment
129 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Allogeneic Stem Cell Transplant, Leukemia, Non-Hodgkins, Lymphoblastic Lymphoma, Myelodysplastic Syndrome, Paroxysmal Nocturnal Hemoglobinuria (PNH)
Interventions
cytoreductive regimen followed by a CD34+E- selected allogeneic stem cell transplant
First posted
2008-01-07
Last updated
2017-03-10
Results first posted
2017-03-10

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryOverall Survival of Transplant Patientsup to 6 yearsCalculate the median overall survival of transplant patients

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYOverall Survival of Transplant Patientsup to 6 yearsDaysMEDIAN

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Overall Survival of Transplant PatientsTransplant Patients727.5Full Range 12 to 2231Days

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDTransplant Patients129
Overall StudyCOMPLETEDTransplant Patients120
Overall StudyNOT COMPLETEDTransplant Patients9

Adverse events30

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAlkaline phosphataseMetabolism and nutrition disordersTransplant Patients2312923
otherBilirubinMetabolism and nutrition disordersTransplant Patients3112931
otherCreatinineMetabolism and nutrition disordersTransplant Patients1312913
otherHemoglobin (Hgb)Blood and lymphatic system disordersTransplant Patients117129117
otherHyperglycemiaMetabolism and nutrition disordersTransplant Patients5812958
otherHyperkalemiaMetabolism and nutrition disordersTransplant Patients2612926
otherHypocalcemiaMetabolism and nutrition disordersTransplant Patients3512935
otherHypokalemiaMetabolism and nutrition disordersTransplant Patients6012960
otherHyponatremiaMetabolism and nutrition disordersTransplant Patients3512935
otherHypophosphatemiaMetabolism and nutrition disordersTransplant Patients4812948

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityTransplant Patients
Total, other adverse eventsTransplant Patients126129
Total, serious adverse eventsTransplant Patients13129

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 comparisons0

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

None in this release.

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/NCT00587054

GET https://conductscience.org/api/trials/v1/NCT00587054/events?page=2