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Comparison · NCT04281472-d754b83d

Stage B: Efgartigimod PH20 SC vs Stage B: Placebo PH20 SC: Stage B: Number of Participants With Improved Functional Level Compared to Stage B Baseline

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. Stage B: Efgartigimod PH20 SC vs Stage B: Placebo PH20 SC: Stage B: Number of Participants With Improved Functional Level Compared to Stage B Baseline. Trial comparisons, record NCT04281472-d754b83d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04281472-d754b83d

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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 10.450.3610.543wilson
Risk in group 20.3640.280.457wilson
Risk difference, group 1 minus group 20.0868-0.04220.212newcombe hybrid score
Risk ratio, group 1 over group 21.240.8981.71log
Odds ratio, group 1 over group 21.430.8372.46log
Number needed to treat, for one more participant with the outcome on Stage B: Efgartigimod PH20 SC than on Stage B: Placebo PH20 SC11.5from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Stage B: Efgartigimod PH20 SCParticipants who completed stage A and received efgartigimod PH20 SC in stage B50111OG000
Group 2Stage B: Placebo PH20 SCParticipants who completed stage A and received placebo PH20 SC in stage B40110OG001

Outcome

Type
SECONDARY
Title
Stage B: Number of Participants With Improved Functional Level Compared to Stage B Baseline
Description
Time frame
Up to 48 weeks during the randomized placebo-controlled stage B
Population
mITT (modified intent-to-treat) analysis set; Participants who were randomized in Stage B and who received at least 1 dose or part of a dose of IMP in Stage B.

Source ClinicalTrials.gov

Trial

Title
A Study to Assess the Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod in Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP, an Autoimmune Disorder That Affects the Peripheral Nerves)
NCT number
NCT04281472
Phases
PHASE2
Conditions
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Interventions
efgartigimod PH20 SC in stage B, placebo in stage B
Lead sponsor
argenx
Results first posted
2024-08-20

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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