Comparison · NCT01700192-2b19f5bf
MK-8237 vs Placebo: Number of Participants Who Discontinue Study Drug Due to an AE
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. MK-8237 vs Placebo: Number of Participants Who Discontinue Study Drug Due to an AE. Trial comparisons, record NCT01700192-2b19f5bf. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01700192-2b19f5bf
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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 | 0.0983 | 0.0789 | 0.122 | wilson | |
| Risk in group 2 | 0.0257 | 0.0165 | 0.0399 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0725 | 0.0485 | 0.0978 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 3.82 | 2.33 | 6.26 | log | |
| Odds ratio, group 1 over group 2 | 4.12 | 2.46 | 6.9 | log | |
| Number needed to treat, for one more participant with the outcome on MK-8237 than on Placebo | 13.8 | 10.2 | 20.6 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | MK-8237 | Participants took MK-8237 12 DU rapidly dissolving tablets administered sublingually q.d. for up to one year. | 73 | 743 | OG000 |
| Group 2 | Placebo | Participants took placebo to MK-8237 rapidly dissolving tablets administered sublingually q.d. for up to one year. | 19 | 738 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Number of Participants Who Discontinue Study Drug Due to an AE
- Description
An AE is defined as any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment.
- Time frame
- Up to 52 weeks
- Population
- The APaT population consists of all randomized participants who received at least 1 dose of study drug (data presented according to actual treatment received).
Source ClinicalTrials.gov
Trial
- Title
- Efficacy and Safety Study of SCH 900237/MK-8237 in Children and Adults With House Dust Mite-Induced Allergic Rhinitis/Rhinoconjunctivitis (P05607)
- NCT number
- NCT01700192
- Phases
- PHASE3
- Conditions
- Rhinitis, Allergic, Perennial, Rhinitis, Allergic, Nonseasonal
- Interventions
MK-8237 tablets, Placebo tablets, Rescue Medication: Self-Injectable Epinephrine, Rescue Medication: Loratadine tablets, Rescue Medication: Olopatadine ophthalmic drops, Rescue Medication: Mometasone furoate nasal spray
- Lead sponsor
- ALK-Abelló A/S
- Results first posted
- 2017-03-03
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01700192?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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