Comparison · NCT04732949-sae
SNG001 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. SNG001 vs Placebo: serious adverse events. Trial comparisons, record NCT04732949-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04732949-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 | 0.126 | 0.0934 | 0.169 | wilson | |
| Risk in group 2 | 0.182 | 0.142 | 0.229 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0553 | -0.113 | 0.00248 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.695 | 0.475 | 1.02 | log | |
| Odds ratio, group 1 over group 2 | 0.652 | 0.416 | 1.02 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on SNG001 than on Placebo | 18.1 | 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 | SNG001 | Patients received SNG001 via inhalation using Ultra nebuliser, once a day for 14 days | 38 | 301 | EG000 |
| Group 2 | Placebo | Patients received Placebo via inhalation using Ultra nebuliser, once a day for 14 days | 55 | 303 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- From the day informed consent is obtained until 28 days after the last administration of the study medication (Day 90).
Source ClinicalTrials.gov
Trial
- Title
- Study to Assess Efficacy and Safety of Inhaled Interferon-β Therapy for COVID-19
- NCT number
- NCT04732949
- Phases
- PHASE3
- Conditions
- Severe Acute Respiratory Syndrome Coronavirus 2, COVID-19
- Interventions
- SNG001, Placebo
- Lead sponsor
- Synairgen Research Ltd.
- Results first posted
- 2023-03-27
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT04732949?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
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GET https://conductscience.org/api/comparisons/v1/NCT04732949-sae