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Trial · NCT00457015

Results by group14

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Mean Symptom Complex Severity (MSCS) Score at 4 Hours Post-doseKALBITOR (Ecallantide)MSCS Score at baseline2.2Standard Deviation 0.50units on a scale
Change From Baseline in Mean Symptom Complex Severity (MSCS) Score at 4 Hours Post-dosePlaceboMSCS Score at baseline2.0Standard Deviation 0.35units on a scale
Change From Baseline in Mean Symptom Complex Severity (MSCS) Score at 4 Hours Post-doseKALBITOR (Ecallantide)MSCS Score at 4 hours post-dose1.4Standard Deviation 0.75units on a scale
Change From Baseline in Mean Symptom Complex Severity (MSCS) Score at 4 Hours Post-dosePlaceboMSCS Score at 4 hours post-dose1.6Standard Deviation 0.77units on a scale
Change From Baseline in Mean Symptom Complex Severity (MSCS) Score at 4 Hours Post-doseKALBITOR (Ecallantide)Change from baseline in MSCS at 4 hours post-dose-0.8Standard Deviation 0.63units on a scale
Change From Baseline in Mean Symptom Complex Severity (MSCS) Score at 4 Hours Post-dosePlaceboChange from baseline in MSCS at 4 hours post-dose-0.4Standard Deviation 0.82units on a scale
Treatment Outcome Score at 4 Hours Post-DoseKALBITOR (Ecallantide)53.4Standard Deviation 49.70units on a scale
Treatment Outcome Score at 4 Hours Post-DosePlacebo8.1Standard Deviation 63.18units on a scale
Patients With Significant Improvement in Overall ResponseKALBITOR (Ecallantide)22participants
Patients With Significant Improvement in Overall ResponsePlacebo12participants
Patients With a Successful Response at 4 Hours Post-dosing, Based on the Change From Baseline in the MSCS ScoreKALBITOR (Ecallantide)45participants
Patients With a Successful Response at 4 Hours Post-dosing, Based on the Change From Baseline in the MSCS ScorePlacebo28participants
Proportion of Patients Maintaining a Significant Improvement in Overall Response Through 24 HoursKALBITOR (Ecallantide)21participants
Proportion of Patients Maintaining a Significant Improvement in Overall Response Through 24 HoursPlacebo10participants

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.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT00457015/results