Comparison · NCT00575185-65d2b578
Valomaciclovir vs Placebo: Number of Participants Who Experienced Adverse Events During the Study Safety and Tolerability
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. Valomaciclovir vs Placebo: Number of Participants Who Experienced Adverse Events During the Study Safety and Tolerability. Trial comparisons, record NCT00575185-65d2b578. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00575185-65d2b578
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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 | 1 | 0.758 | 1 | wilson | |
| Risk in group 2 | 1 | 0.741 | 1 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.242 | 0.259 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1 | 1 | 1 | log | |
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to treat | from the risk difference interval | the two groups' risks are equal |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Valomaciclovir | Valomaciclovir 2 grams orally twice daily for 21 days~Valomaciclovir: 4 grams orally of valomaciclovir (2 grams BID) for 21 days. | 12 | 12 | OG000 |
| Group 2 | Placebo | placebo 2 tablets twice daily for 21 days~placebo: Placebo tablets orally twice daily for 21 days. | 11 | 11 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants Who Experienced Adverse Events During the Study Safety and Tolerability
- Description
- Assessing adverse events in participants to see if this drug causes more or less side effects
- Time frame
- 15 days
- Population
Source ClinicalTrials.gov
Trial
- Title
- Activity of Valomaciclovir in Infectious Mononucleosis Due to Primary Epstein-Barr Virus Infection
- NCT number
- NCT00575185
- Phases
- PHASE1, PHASE2
- Conditions
- Infectious Mononucleosis
- Interventions
- Valomaciclovir, placebo
- Lead sponsor
- University of Minnesota
- Results first posted
- 2015-03-17
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00575185?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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