Comparison · NCT03809429-sae
FE 999049 + GnRH Agonist (GONAPEPTYL) vs FE 999049 + GnRH Antagonist (CETROTIDE): 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. FE 999049 + GnRH Agonist (GONAPEPTYL) vs FE 999049 + GnRH Antagonist (CETROTIDE): serious adverse events. Trial comparisons, record NCT03809429-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03809429-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 | 0.0198 | 0.00773 | 0.0498 | wilson | |
| Risk in group 2 | 0.0294 | 0.0135 | 0.0627 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00961 | -0.045 | 0.0243 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.673 | 0.193 | 2.35 | log | |
| Odds ratio, group 1 over group 2 | 0.667 | 0.185 | 2.4 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on FE 999049 + GnRH Agonist (GONAPEPTYL) than on FE 999049 + GnRH Antagonist (CETROTIDE) | 104 | 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 | FE 999049 + GnRH Agonist (GONAPEPTYL) | FE 999049 + GnRH agonist (GONAPEPTYL): Pre-filled injection pen | 4 | 202 | EG000 |
| Group 2 | FE 999049 + GnRH Antagonist (CETROTIDE) | FE 999049 + GnRH antagonist (CETROTIDE): Powder and solvent for solution for injection | 6 | 204 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events were recorded from signing of the informed consent until end-of-trial (approximately 7 months).
Source ClinicalTrials.gov
Trial
- Title
- Follitropin Delta in Long GnRH Agonist and GnRH Antagonist Protocols (BEYOND)
- NCT number
- NCT03809429
- Phases
- PHASE3
- Conditions
- Infertility, Female
- Interventions
- FE 999049 + GnRH agonist (GONAPEPTYL), FE 999049 + GnRH antagonist (CETROTIDE)
- Lead sponsor
- Ferring Pharmaceuticals
- Results first posted
- 2024-05-13
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03809429?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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