Comparison · NCT05168774-sae
Low Dose (20-30mg) vs High Dose (40-60 mg): 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. Low Dose (20-30mg) vs High Dose (40-60 mg): serious adverse events. Trial comparisons, record NCT05168774-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05168774-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 | 0.25 | 0.0715 | 0.591 | wilson | |
| Risk in group 2 | 0.25 | 0.0715 | 0.591 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.385 | 0.385 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1 | 0.183 | 5.46 | log | |
| Odds ratio, group 1 over group 2 | 1 | 0.104 | 9.61 | log | |
| Number needed to harm | from the risk difference interval | the two groups' risks are equal |
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 | Low Dose (20-30mg) | Subjects will receive daily subcutaneous (SC) dosing of Elamipretide (20-30 mg) for 52 weeks~Elamipretide: Elamipretide is a tetra peptide with limited blood brain barrier penetration being developed for use in a variety of mitochondrial disorders, including FRDA, mitochondrial myopathy and Barth Syndrome. | 2 | 8 | EG000 |
| Group 2 | High Dose (40-60 mg) | Subjects will receive daily subcutaneous (SC) dosing of Elamipretide (40-60 mg) for 52 weeks~Elamipretide: Elamipretide is a tetra peptide with limited blood brain barrier penetration being developed for use in a variety of mitochondrial disorders, including FRDA, mitochondrial myopathy and Barth Syndrome. | 2 | 8 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- AE's were assessed for approximately 104 weeks (2 years).
Source ClinicalTrials.gov
Trial
- Title
- FRDA Investigator Initiated Study (IIS) With Elamipretide
- NCT number
- NCT05168774
- Phases
- PHASE1, PHASE2
- Conditions
- Friedreich Ataxia
- Interventions
- Elamipretide
- Lead sponsor
- Children's Hospital of Philadelphia
- Results first posted
- 2025-12-12
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT05168774?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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