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Trial · NCT01095497

Results by group165

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

OutcomeGroupCategoryValueSpreadUnits
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Intravenous (IV) CINRYZENumber of subjects with adverse events120.019Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Subcutaneous (SC) CINRYZE Dose 1Number of subjects with adverse events100.027Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.SC CINRYZE Dose 2Number of subjects with adverse events110.010Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Intravenous (IV) CINRYZENumber of subjects with injection site reactions10.033Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Subcutaneous (SC) CINRYZE Dose 1Number of subjects with injection site reactions100.032Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.SC CINRYZE Dose 2Number of subjects with injection site reactions110.010Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Intravenous (IV) CINRYZENumber of subjects who discontinued study drug1Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Subcutaneous (SC) CINRYZE Dose 1Number of subjects who discontinued study drug0Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.SC CINRYZE Dose 2Number of subjects who discontinued study drug0Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Intravenous (IV) CINRYZENumber of subjects who withdrew from the study1Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.Subcutaneous (SC) CINRYZE Dose 1Number of subjects who withdrew from the study1Participants
Incidence and Severity of Adverse Events, Number of Subjects With Local Injection Site Reactions, and Number of Subjects Who Discontinue Study Drug or Withdraw From the Study.SC CINRYZE Dose 2Number of subjects who withdrew from the study0Participants
Mean Change C1 Inhibitor (C1INH)Intravenous (IV) CINRYZE1 hour (h) post Dose 10.075Standard Deviation 0.023g/L
Mean Change C1 Inhibitor (C1INH)Subcutaneous (SC) CYNRYZE Dose 11 hour (h) post Dose 1-0.002Standard Deviation 0.008g/L
Mean Change C1 Inhibitor (C1INH)SC Dose 21 hour (h) post Dose 1-0.001Standard Deviation 0.006g/L
Mean Change C1 Inhibitor (C1INH)Intravenous (IV) CINRYZE2 h post Dose 10.070Standard Deviation 0.021g/L
Mean Change C1 Inhibitor (C1INH)Subcutaneous (SC) CYNRYZE Dose 12 h post Dose 1-0.002Standard Deviation 0.008g/L
Mean Change C1 Inhibitor (C1INH)SC Dose 22 h post Dose 1-0.001Standard Deviation 0.004g/L
Mean Change C1 Inhibitor (C1INH)Intravenous (IV) CINRYZE3 h post Dose 10.070Standard Deviation 0.023g/L
Mean Change C1 Inhibitor (C1INH)Subcutaneous (SC) CYNRYZE Dose 13 h post Dose 1-0.002Standard Deviation 0.007g/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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