Comparison · NCT03426345-7c6d258b
Relamorelin 10 μg vs Placebo: Number of Participants With a ≥1% Increase in Glycosylated Hemoglobin A1c (HBA1c)
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. Relamorelin 10 μg vs Placebo: Number of Participants With a ≥1% Increase in Glycosylated Hemoglobin A1c (HBA1c). Trial comparisons, record NCT03426345-7c6d258b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03426345-7c6d258b
On this page
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 | 0.735 | 0.66 | 0.799 | wilson | |
| Risk in group 2 | 0.548 | 0.467 | 0.626 | wilson | |
| Risk difference, group 1 minus group 2 | 0.187 | 0.0782 | 0.29 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.34 | 1.13 | 1.6 | log | |
| Odds ratio, group 1 over group 2 | 2.29 | 1.41 | 3.72 | log | |
| Number needed to treat, for one more participant with the outcome on Relamorelin 10 μg than on Placebo | 5.34 | 3.44 | 12.8 | 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 | Relamorelin 10 μg | Following a 2-week placebo run-in, participants received relamorelin 10 μg injected subcutaneously twice daily for up to 12 weeks. | 111 | 151 | OG001 |
| Group 2 | Placebo | Following a 2-week placebo run-in, participants received placebo-matching relamorelin injected subcutaneously twice daily for up to 12 weeks. | 80 | 146 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With a ≥1% Increase in Glycosylated Hemoglobin A1c (HBA1c)
- Description
- Time frame
- Baseline (Day 1) up to 12 weeks
- Population
Safety Population included all participants who received ≥1 administration of double-blind study treatment. Overall number analyzed is the number of participants with non-PCS baseline values and at least one post-baseline assessment.
Source ClinicalTrials.gov
Trial
- Title
- Study to Evaluate the Safety and Efficacy of Relamorelin in Participants With Diabetic Gastroparesis Study 02
- NCT number
- NCT03426345
- Phases
- PHASE3
- Conditions
- Gastroparesis, Diabetes Mellitus
- Interventions
- Placebo, Relamorelin
- Lead sponsor
- Allergan
- Results first posted
- 2021-08-06
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03426345?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
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT03426345-7c6d258b