Comparison · NCT04300309-409ff2c3
Cohort 1 vs Cohort 2: Number of Participants With Adverse Events (AEs)
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. Cohort 1 vs Cohort 2: Number of Participants With Adverse Events (AEs). Trial comparisons, record NCT04300309-409ff2c3. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04300309-409ff2c3
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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 | 0.773 | 0.566 | 0.899 | wilson | |
| Risk in group 2 | 0.667 | 0.3 | 0.903 | wilson | |
| Risk difference, group 1 minus group 2 | 0.106 | -0.208 | 0.494 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.16 | 0.63 | 2.13 | log | |
| Odds ratio, group 1 over group 2 | 1.7 | 0.237 | 12.2 | log | |
| Number needed to treat, for one more participant with the outcome on Cohort 1 than on Cohort 2 | 9.43 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Cohort 1 | Infants \>28 days of age treated with artemether-lumefantrine (5 mg:60 mg) twice daily for 3 days | 17 | 22 | OG000 |
| Group 2 | Cohort 2 | Term neonates 1-28 days of age treated with artemether-lumefantrine (5 mg:60 mg) twice daily for 3 days | 4 | 6 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Adverse Events (AEs)
- Description
- Number of participants with adverse events (any AEs regardless of seriousness), including changes in laboratory results qualifying and reported as adverse events.
- Time frame
- From first dose of study treatment until Day 43
- Population
- Safety Set, including all patients who received at least one dose of study treatment
Source ClinicalTrials.gov
Trial
- Title
- Pharmacokinetics, Safety, Tolerability and Efficacy of a New Artemether-lumefantrine Dispersible Tablet in Infants and Neonates <5 kg Body Weight With Acute Uncomplicated Plasmodium Falciparum Malaria
- NCT number
- NCT04300309
- Phases
- PHASE2, PHASE3
- Conditions
- Plasmodium Falciparum Malaria
- Interventions
- artemether:lumefantrine (2.5 mg:30 mg)
- Lead sponsor
- Novartis Pharmaceuticals
- Results first posted
- 2024-10-03
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT04300309?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.
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