ConductScience.org, home

Comparison · NCT02753530-deaths

Arimoclomol (20 Months) vs Placebo (20 Months): deaths from any cause

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

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

Download JSON
Cite this record

ConductScience Library. Arimoclomol (20 Months) vs Placebo (20 Months): deaths from any cause. Trial comparisons, record NCT02753530-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02753530-deaths

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.01370.002420.0736wilson
Risk in group 20.01280.002270.0691wilson
Risk difference, group 1 minus group 20.000878-0.05650.0617newcombe hybrid score
Risk ratio, group 1 over group 21.070.068116.8log
Odds ratio, group 1 over group 21.070.065717.4log
Number needed to harm, for one more death from any cause on Arimoclomol (20 Months) than on Placebo (20 Months)1,140from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Arimoclomol (20 Months)Arimoclomol base 248 mg 3 times daily for 20 months173EG000
Group 2Placebo (20 Months)Matching placebo 3 times daily for 20 months178EG001

Harm

What it counts
Total, all-cause mortality
Time frame
From first dose of study medication until 14 days following the latest administration of study medication. Assessed monthly for the first 6 months, and then every second month until Month 20.

Source ClinicalTrials.gov

Trial

Title
Study of Arimoclomol in Inclusion Body Myositis (IBM)
NCT number
NCT02753530
Phases
PHASE2
Conditions
Inclusion Body Myositis
Interventions
Arimoclomol, Placebo
Lead sponsor
ZevraDenmark
Results first posted
2023-05-10

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT02753530-deaths