Comparison · NCT00326625-deaths
Glatiramer Acetate 40mg vs Placebo: 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
Cite this record
ConductScience Library. Glatiramer Acetate 40mg vs Placebo: deaths from any cause. Trial comparisons, record NCT00326625-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00326625-deaths
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.12 | 0.0803 | 0.174 | wilson | |
| Risk in group 2 | 0.0934 | 0.0591 | 0.144 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0262 | -0.0383 | 0.0908 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.28 | 0.703 | 2.33 | log | |
| Odds ratio, group 1 over group 2 | 1.32 | 0.675 | 2.57 | log | |
| Number needed to harm, for one more death from any cause on Glatiramer Acetate 40mg than on Placebo | 38.2 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Glatiramer Acetate 40mg | Pre-filled syringe of 40 mg glatiramer acetate (GA) for injection, administered subcutaneously once a day | 22 | 184 | EG000 |
| Group 2 | Placebo | Pre-filled syringe of matching placebo, administered subcutaneously once a day | 17 | 182 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, all-cause mortality
- Time frame
- Baseline up to 96 weeks.
Source ClinicalTrials.gov
Trial
- Title
- Clinical Trial of Glatiramer Acetate in Amyotrophic Lateral Sclerosis (ALS)
- NCT number
- NCT00326625
- Phases
- PHASE2
- Conditions
- Amyotrophic Lateral Sclerosis
- Interventions
- 40 mg glatiramer acetate, Placebo
- Lead sponsor
- Teva Pharmaceutical Industries, Ltd.
- Results first posted
- 2021-10-20
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00326625?tab=results
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.
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GET https://conductscience.org/api/comparisons/v1/NCT00326625-deaths