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Trial · NCT00588536

Study of Sequential Administration of Oral 6-Thioguanine After Methotrexate in Patients With LCH

NCT00588536, Phase 2, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2015-05-04

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study of Sequential Administration of Oral 6-Thioguanine After Methotrexate in Patients With LCH. Trials, record NCT00588536. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00588536

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Trial

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

Title
Study of Sequential Administration of Oral 6-Thioguanine After Methotrexate in Patients With LCH
NCT number
NCT00588536
Status
Completed
Phases
Phase 2
Enrollment
5 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Langerhans Cell Histiocytosis
Interventions
Methotrexate, 6-Thioguanine, Leucovorin Calcium
First posted
2008-01-08
Last updated
2015-05-04
Results first posted
2015-05-04

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
Primary
Determine the Incidence of Complete and Partial Response and the Duration of Response in Patients With Langerhans Cell Histiocytosis (LCH) Treated With Sequential Administration of Oral 6-TG After MTX.
Conclusion of the study

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARY
Determine the Incidence of Complete and Partial Response and the Duration of Response in Patients With Langerhans Cell Histiocytosis (LCH) Treated With Sequential Administration of Oral 6-TG After MTX.
Conclusion of the studyparticipantsNUMBER

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Determine the Incidence of Complete and Partial Response and the Duration of Response in Patients With Langerhans Cell Histiocytosis (LCH) Treated With Sequential Administration of Oral 6-TG After MTX.
MTX, 6-TG and LeucovorinComplete Response2participants
Determine the Incidence of Complete and Partial Response and the Duration of Response in Patients With Langerhans Cell Histiocytosis (LCH) Treated With Sequential Administration of Oral 6-TG After MTX.
MTX, 6-TG and LeucovorinStable Disease1participants
Determine the Incidence of Complete and Partial Response and the Duration of Response in Patients With Langerhans Cell Histiocytosis (LCH) Treated With Sequential Administration of Oral 6-TG After MTX.
MTX, 6-TG and LeucovorinProgression of Disease2participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMTX, 6-TG and Leucovorin5
Overall StudyCOMPLETEDMTX, 6-TG and Leucovorin5
Overall StudyNOT COMPLETEDMTX, 6-TG and Leucovorin0

Adverse events18

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal pain/crampingGastrointestinal disordersMTX, 6-TG and Leucovorin151
otherAnorexiaMetabolism and nutrition disordersMTX, 6-TG and Leucovorin151
otherBlood bilirubin increasedInvestigationsMTX, 6-TG and Leucovorin151
otherBone painMusculoskeletal and connective tissue disordersMTX, 6-TG and Leucovorin151
otherSore throatRespiratory, thoracic and mediastinal disordersMTX, 6-TG and Leucovorin152
otherCreatinine increasedInvestigationsMTX, 6-TG and Leucovorin151
otherDiarrheaGastrointestinal disordersMTX, 6-TG and Leucovorin151
otherHeadacheNervous system disordersMTX, 6-TG and Leucovorin151
otherAnemiaBlood and lymphatic system disordersMTX, 6-TG and Leucovorin4510
otherHypomagnesemiaMetabolism and nutrition disordersMTX, 6-TG and Leucovorin151

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMTX, 6-TG and Leucovorin
Total, other adverse eventsMTX, 6-TG and Leucovorin55
Total, serious adverse eventsMTX, 6-TG and Leucovorin25

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/NCT00588536

GET https://conductscience.org/api/trials/v1/NCT00588536/registered