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Trial · NCT03650400

Results by group12

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Pharmacokinetics of Fevipiprant by Area Under the Curve From 0 to 24 Hours at Steady State (AUC0-24h,ss), After at Least Four Consecutive Days of DosingCohort A Fevipiprant 75 mg2380Standard Deviation 1880h*ng/mL
Pharmacokinetics of Fevipiprant by Maximum Plasma Concentration at Steady State (Cmax,ss), After at Least Four Consecutive Days of DosingCohort A Fevipiprant 75 mg394Standard Deviation 286ng/mL
Pharmacokinetics of Fevipiprant by Oral Clearance at Steady State (CL/F), After at Least Four Consecutive Days of DosingCohort A Fevipiprant 75 mg48.2Standard Deviation 32L/h
Pharmacokinetics of Fevipiprant by CL/FCohort A Fevipiprant 75 mg48.2Standard Deviation 32.0L/h
Pharmacokinetics of Fevipiprant by Tmax,ssCohort A Fevipiprant 75 mg1.42Standard Deviation 0.916h
Urinary Excretion of FevipiprantCohort A Fevipiprant 75 mg6.61Standard Deviation 4.88L/h
Pharmacokinetics of Fevipiprant by Cmin,ssCohort A Fevipiprant 75 mg28.3Standard Deviation 13.8ng/mL
Pharmacokinetics of the Metabolite CCN362 by AUC0-24h,ssCohort A Fevipiprant 75 mg2760Standard Deviation 1210h*ng/mL
Pharmacokinetics of the Metabolite CCN362 by Cmax,ssCohort A Fevipiprant 75 mg302Standard Deviation 134ng/mL
Pharmacokinetics of the Metabolite CCN362 by Cmin,ssCohort A Fevipiprant 75 mg33.6Standard Deviation 22.6ng/mL
Pharmacokinetics of the Metabolite CCN362 by Tmax,ssCohort A Fevipiprant 75 mg2.69Standard Deviation 1.20h
Urinary Excretion of the Metabolite, CCN362Cohort A Fevipiprant 75 mg5.10Standard Deviation 1.96L/h

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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