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Trial · NCT00438815

Results by group21

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

OutcomeGroupCategoryValueSpreadUnits
Number of Hereditary Angioedema (HAE) Attacks Treated With C1INH-nfOpen-label C1INH-nfConservative Analysis609attacks
Number of Hereditary Angioedema (HAE) Attacks Treated With C1INH-nfOpen-label C1INH-nfLess Conservative Analysis598attacks
Time to Beginning of Substantial Relief of the Defining SymptomOpen-label C1INH-nf0.7595% Confidence Interval 0.50 to 1.00hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 11.5095% Confidence Interval 0.75 to 4.00hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 20.5095% Confidence Interval 0.25 to 2.50hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 30.5095% Confidence Interval 0.50 to 0.75hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 40.5095% Confidence Interval 0.25 to 1.00hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 50.7595% Confidence Interval 0.50 to 1.25hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 60.5095% Confidence Interval 0.25 to 1.25hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 70.7595% Confidence Interval 0.50 to 0.75hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 80.5095% Confidence Interval 0.25 to 0.75hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 90.2595% Confidence Interval 0.25 to 0.50hours
Time to Beginning of Substantial Relief of the Defining Symptom for Subjects Who Received Multiple TreatmentsOpen-label C1INH-nfAttack number 100.5095% Confidence Interval 0.25 to 0.75hours
Antigenic C1 Inhibitor (C1INH) Serum LevelsOpen-label C1INH-nfPre-infusion10.7Standard Deviation 13.91mg/dL
Antigenic C1 Inhibitor (C1INH) Serum LevelsOpen-label C1INH-nfIncrease at 1 hour post-infusion9.6Standard Deviation 12.98mg/dL
Functional C1INH Serum LevelsOpen-label C1INH-nfPre-infusion27.0Standard Deviation 19.30percent of functional C1INH
Functional C1INH Serum LevelsOpen-label C1INH-nfPercent increase at 1 hour post-infusion39.2Standard Deviation 18.04percent of functional C1INH
Complement C4 Serum LevelsOpen-label C1INH-nfPre-infusion5.3Standard Deviation 5.41mg/dL
Complement C4 Serum LevelsOpen-label C1INH-nfChange at 1 hour post-infusion-0.2Standard Deviation 1.51mg/dL
Percent of HAE Attacks With Substantial Relief of the Defining SymptomOpen-label C1INH-nfConservative Analysis87percent of attacks

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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