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Comparison · NCT03296527-sae

FE 000049 (Follitropin Delta) 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

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ConductScience Library. FE 000049 (Follitropin Delta) vs GONAL-F (Follitropin Alfa): serious adverse events. Trial comparisons, record NCT03296527-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03296527-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.06010.04240.0845wilson
Risk in group 20.03530.02240.0551wilson
Risk difference, group 1 minus group 20.0248-0.001720.0524newcombe hybrid score
Risk ratio, group 1 over group 21.70.9623.02log
Odds ratio, group 1 over group 21.750.9623.18log
Number needed to harm, for one more participant with a serious adverse event on FE 000049 (Follitropin Delta) than on GONAL-F (Follitropin Alfa)40.3from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1FE 000049 (Follitropin Delta)
FE 999049 was administered as single daily subcutaneous injections in the abdomen. Participants randomized to FE 999049 had their individual dose determined on the basis of their AMH level at screening and their body weight at randomization. The daily FE 999049 dose was fixed throughout the stimulation period and minimum and maximum allowed daily dose was 6 and 12 μg, respectively. Dosing continued until the criterion for triggering of final follicular maturation was met. Participants could be treated for a maximum of 20 days.
30499EG000
Group 2GONAL-F (Follitropin Alfa)
GONAL-F was administered as single daily subcutaneous injections in the abdomen. The starting dose of GONAL-F was 150 IU and fixed for the first five stimulation days, after which it could be adjusted by 75 IU based on the individual response. The maximum allowed daily dose was 450 IU. Dosing continued until the criterion for triggering of final follicular maturation was met. Participants could be treated for a maximum of 20 days.
18510EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were recorded from screening up to end-of-trial (up to approximately 5.5 months).

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of FE 999049 in Controlled Ovarian Stimulation in Pan-Asian Women
NCT number
NCT03296527
Phases
PHASE3
Conditions
Controlled Ovarian Simulation
Interventions
Follitropin alfa, Follitropin delta
Lead sponsor
Ferring Pharmaceuticals
Results first posted
2021-06-01

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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