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Comparison · NCT00071799-e83d4998

Azacitidine vs Conventional Care: Number of Participants Who Died

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Azacitidine vs Conventional Care: Number of Participants Who Died. Trial comparisons, record NCT00071799-e83d4998. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00071799-e83d4998

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.4580.3870.531wilson
Risk in group 20.6310.5590.699wilson
Risk difference, group 1 minus group 2-0.173-0.271-0.0701newcombe hybrid score
Risk ratio, group 1 over group 20.7260.5970.882log
Odds ratio, group 1 over group 20.4940.3240.753log
Number needed to treat, for one fewer participant with the outcome on Azacitidine than on Conventional Care5.773.6914.3from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1AzacitidineAzacitidine, 75 mg/m\^2/day given by subcutaneous injection for 7 days of every 28 day cycle, plus best supportive care.82179OG000
Group 2Conventional CarePhysician choice of low dose cytarabine, standard chemotherapy, or best supportive care (consisting of blood products, growth factors, antibiotics)113179OG001

Outcome

Type
PRIMARY
Title
Number of Participants Who Died
Description
Count of participants who died during the study
Time frame
42 months
Population
Intent to treat population

Source ClinicalTrials.gov

Trial

Title
A Survival Study in Patients With High Risk Myelodysplastic Syndromes Comparing Azacitidine Versus Conventional Care
NCT number
NCT00071799
Phases
PHASE3
Conditions
Myelodysplastic Syndromes
Interventions
Azacitidine, Physician Choice
Lead sponsor
Celgene
Results first posted
2010-07-05

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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