Comparison · NCT00261833-sae
Zemaira® vs Placebo: serious adverse events
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. Zemaira® vs Placebo: serious adverse events. Trial comparisons, record NCT00261833-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00261833-sae
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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 | 0.301 | 0.217 | 0.401 | wilson | |
| Risk in group 2 | 0.322 | 0.233 | 0.426 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0208 | -0.154 | 0.113 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.935 | 0.606 | 1.44 | log | |
| Odds ratio, group 1 over group 2 | 0.908 | 0.483 | 1.71 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Zemaira® than on Placebo | 48.2 | 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 | Zemaira® | Alpha1-proteinase inhibitor: 60 mg/kg body weight/week intravenous | 28 | 93 | EG000 |
| Group 2 | Placebo | Lyophilized preparation: 60 mg/kg body weight/week intravenous | 28 | 87 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- For the duration of the study (25 months; 1 month screening period, 24 months treatment period).
Source ClinicalTrials.gov
Trial
- Title
- Zemaira in Subjects With Emphysema Due to Alpha1-Proteinase Inhibitor Deficiency
- NCT number
- NCT00261833
- Phases
- PHASE4
- Conditions
- Alpha1-proteinase Inhibitor Deficiency, Emphysema
- Interventions
- Alpha1-proteinase inhibitor, Placebo
- Lead sponsor
- CSL Behring
- Results first posted
- 2015-01-19
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00261833?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.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT00261833-sae