Comparison · NCT01121666-sae
AFOLIA-150 (Follitropin Alfa) vs Gonal-f® (Follitropin Alfa): 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. AFOLIA-150 (Follitropin Alfa) vs Gonal-f® (Follitropin Alfa): serious adverse events. Trial comparisons, record NCT01121666-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01121666-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 | 0.0482 | 0.0278 | 0.0823 | wilson | |
| Risk in group 2 | 0.0244 | 0.00833 | 0.0693 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0238 | -0.0255 | 0.0615 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.98 | 0.568 | 6.87 | log | |
| Odds ratio, group 1 over group 2 | 2.03 | 0.561 | 7.31 | log | |
| Number needed to harm, for one more participant with a serious adverse event on AFOLIA-150 (Follitropin Alfa) than on Gonal-f® (Follitropin Alfa) | 42 | 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 | AFOLIA-150 (Follitropin Alfa) | Follitropin alfa: 150IU per day subcutaneously for a maximum of 16 days | 12 | 249 | EG000 |
| Group 2 | Gonal-f® (Follitropin Alfa) | Follitropin alfa: 150IU per day subcutaneously for a maximum of 16 days | 3 | 123 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Study period + 30 days
Source ClinicalTrials.gov
Trial
- Title
- Multi-centre Study to Compare Efficacy and Safety of AFOLIA and Gonal-f in Women for Assisted Reproductive Treatment
- NCT number
- NCT01121666
- Phases
- PHASE3
- Conditions
- Infertility
- Interventions
- Follitropin alfa
- Lead sponsor
- Finox AG
- Results first posted
- 2016-04-15
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01121666?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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