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Trial · NCT00504764

Treatment of Relapsed Promyelocytic Leukemia With Arsenic Trioxide (ATO)

NCT00504764, Phase 4, Completed, PETHEMA Foundation

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Treatment of Relapsed Promyelocytic Leukemia With Arsenic Trioxide (ATO). Trials, record NCT00504764. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00504764

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Trial

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

Title
Treatment of Relapsed Promyelocytic Leukemia With Arsenic Trioxide (ATO)
NCT number
NCT00504764
Status
Completed
Phases
Phase 4
Enrollment
60 participants, estimated
Lead sponsor
PETHEMA Foundation
Conditions
Acute Promyelocytic Leukemia
Interventions
Arsenic Trioxide, Autologous Transplantation, Allogenic Transplantation, ATRA
First posted
2007-07-20
Last updated
2014-10-28

Source ClinicalTrials.gov

Registered outcomes7

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

ListOutcomeTime frameDescription
PrimaryEvaluate the hematological and molecular remission rate after induction and consolidation with ATO1 year
PrimaryEvaluate the induction mortality with ATO in monotherapy1 year
PrimaryEvaluate the hematological and molecular relapse rate in patients treated with autologous transplantation, allogenic transplantation or ATO + ATRA +/- Mylotarg1 year
SecondaryEvaluate kinetics of the MDR of PML/RARa during and after ATO2 years
SecondaryEvaluate the mortality related with postremission treatment1 year
SecondarySide effects of ATO and the different treatments post-consolidation2 years
SecondaryOverall survival2 years

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

Adverse events0

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

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

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/NCT00504764

GET https://conductscience.org/api/trials/v1/NCT00504764/registered