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Trial · NCT04812925

Registered outcomes28

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
SecondaryPharmacodynamics markers: total IgGUp to 52 weeks
SecondaryPercentage of participants who performed self-administration at home over timeUp to 52 weeks
SecondaryPercentage of caregivers who administered the injection to the patient at home over timeUp to 52 weeks
SecondaryNumber of training visits needed for the participant or caregiver to be competent to start administering efgartigimod PH20 SCUp to 52 weeks
SecondaryPercentage of self- or caregiver-supported administrations at homeUp to 52 weeks
SecondaryIncidence of antibodies to efgartigimodUp to 216 weeks
SecondaryTiters of antibodies to efgartigimodUp to 216 weeks
SecondaryPresence of NAb against efgartigimodUp to 216 weeksNAb : Neutralizing antibodies

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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