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Trial · NCT01386658

Results by group144

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

OutcomeGroupCategoryValueSpreadUnits
Time to Peak Concentration (Tmax) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal0.42Standard Deviation 0.13Hour (h)
Time to Peak Concentration (Tmax) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack0.55Standard Deviation 0.19Hour (h)
Time to Peak Concentration (Tmax) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: Without Acute Attack0.57Standard Deviation 0.17Hour (h)
Maximum Plasma Concentration (Cmax) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal659Standard Deviation 158Nanogram per milliliter (ng/mL)
Maximum Plasma Concentration (Cmax) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack805Standard Deviation 125Nanogram per milliliter (ng/mL)
Maximum Plasma Concentration (Cmax) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: Without Acute Attack761Standard Deviation 133Nanogram per milliliter (ng/mL)
Total Plasma Clearance (CL/F) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal10.8Standard Deviation 4.63Milliliters per minute (mL/min)
Total Plasma Clearance (CL/F) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack13.1Standard Deviation 3.42Milliliters per minute (mL/min)
Total Plasma Clearance (CL/F) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: Without Acute Attack19.3Standard Deviation 4.84Milliliters per minute (mL/min)
Area Under the Plasma Concentration-time Curve From Time Zero to 4 Hours Post-dose (AUC0-4) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal1241Standard Deviation 319Hour*nanogram per milliliter (h*ng/mL)
Area Under the Plasma Concentration-time Curve From Time Zero to 4 Hours Post-dose (AUC0-4) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack1448Standard Deviation 304Hour*nanogram per milliliter (h*ng/mL)
Area Under the Plasma Concentration-time Curve From Time Zero to 4 Hours Post-dose (AUC0-4) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: Without Acute Attack1335Standard Deviation 211Hour*nanogram per milliliter (h*ng/mL)
Area Under the Plasma Concentration-time Curve From Time Zero to 6 Hours Post-dose (AUC0-t) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal1289Standard Deviation 325h*ng/mL
Area Under the Plasma Concentration-time Curve From Time Zero to 6 Hours Post-dose (AUC0-t) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack1573Standard Deviation 372h*ng/mL
Area Under the Plasma Concentration-time Curve From Time Zero to 6 Hours Post-dose (AUC0-t) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: Without Acute Attack1398Standard Deviation 225h*ng/mL
Area Under the Plasma Concentration-time Curve From Time Zero to Infinity (AUC0-inf) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal1243Standard Deviation 244h*ng/mL
Area Under the Plasma Concentration-time Curve From Time Zero to Infinity (AUC0-inf) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack1710Standard Deviation 569h*ng/mL
Area Under the Plasma Concentration-time Curve From Time Zero to Infinity (AUC0-inf) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: Without Acute Attack1416Standard Deviation 229h*ng/mL
Volume of Distribution (Vz/F) of a Single Subcutaneous (SC) Dose of IcatibantPrepubertal12.5Standard Deviation 5.28Liters (L)
Volume of Distribution (Vz/F) of a Single Subcutaneous (SC) Dose of IcatibantPubertal/Postpubertal: With Acute Attack23.5Standard Deviation 13.9Liters (L)

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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