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Trial · NCT07262983

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryIncidence of SAEs, AEs requiring study drug discontinuation.Through end of studyTo determine the safety and tolerability of JAK inhibitor treatment (baricitinib) in patients with Job s syndrome with lupus-like disease and/or AD.
SecondaryIncidence of Candida and/or bacterial infections.Through end of studyTo assess changes in Candida and/or bacterial infections
SecondaryMean change in CLASI score from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To evaluate the effect of baricitinib on lupus-like features.
SecondaryMean change in EASI score from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To evaluate the effect of baricitinib on AD.
SecondaryMean change in SLEDAI score from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To evaluate the effect of baricitinib on lupus-like features.
SecondaryMean change in the PGA score from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To evaluate the effect of baricitinib on lupus-like features and AD.
SecondaryMean change in the SF-36 score (adults) from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To investigate the effect of baricitinib on QOL.
SecondaryMean change in the PROMIS score from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To investigate the effect of baricitinib on QOL.
SecondaryMean change in the DLQI score (adults) from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To investigate the effect of baricitinib on QOL.
SecondaryMean change in the CDLQI score (pediatrics) from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To investigate the effect of baricitinib on QOL.
SecondaryMean change in the PedsQL score (pediatrics) from day -90 to day 0 and then from day 0 to days 90 and 180.From day -90 to day 0 and then from day 0 to days 90 and 180To investigate the effect of baricitinib on QOL.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license 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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