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Disease · MONDO_0019623

Comparisons in its trials14

Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
KALBITOR (Ecallantide) vs Placebo: Patients With Significant Improvement in Overall Response22 of 4812 of 4896NCT00457015Trial comparisons
KALBITOR (Ecallantide) vs Placebo: serious adverse events0 of 483 of 4896NCT00457015Trial comparisons
KALBITOR (Ecallantide) vs Placebo: Proportion of Patients Maintaining a Significant Improvement in Overall Response Through 24 Hours21 of 4810 of 4795NCT00457015Trial comparisons
KALBITOR (Ecallantide) vs Placebo: Patients With a Successful Response at 4 Hours Post-dosing, Based on the Change From Baseline in the MSCS Score45 of 4828 of 4795NCT00457015Trial comparisons
C1INH-nf vs Placebo: serious adverse events0 of 710 of 1283NCT00289211Trial comparisons
rhC1INH vs Placebo (Saline): serious adverse events1 of 560 of 1874NCT01188564Trial comparisons
C1INH-nf vs Placebo: Number of Subjects With Beginning of Substantial Relief of the Defining Symptom21 of 3514 of 3368NCT00289211Trial comparisons
Prepubertal vs Pubertal/Postpubertal: Number of Participants With Adverse Events (AEs)2 of 1111 of 2132NCT01386658Trial comparisons
Prepubertal vs Pubertal/Postpubertal: Number of Participants With Clinically Significant Changes in Clinical Laboratory Evaluations0 of 110 of 2132NCT01386658Trial comparisons
Prepubertal vs Pubertal/Postpubertal: Number of Participants With Clinically Significant Changes in Reproductive Hormones0 of 110 of 2132NCT01386658Trial comparisons
Prepubertal vs Pubertal/Postpubertal: Number of Participants With Clinically Significant Changes in Vital Signs0 of 110 of 2132NCT01386658Trial comparisons
Prepubertal vs Pubertal/Postpubertal: Number of Participants Who Reported Presence of Anti-icatibant Antibodies0 of 110 of 2132NCT01386658Trial comparisons
Prepubertal vs Pubertal/Postpubertal: Number of Participants With Clinically Significant Changes in Electrocardiograms (ECGs)0 of 110 of 2132NCT01386658Trial comparisons
Subcutaneous (SC) CINRYZE With Recombinant Human Hyaluronidase ph20 (rHuPH20) Dose Level 1 vs SC CINRYZE With rHuPH20 Dose Level 2: serious adverse events0 of 60 of 612NCT01426763Trial comparisons

diseases-2026-09-18-0.1.0

Sources 6

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
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
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/diseases/v1/MONDO_0019623/comparisons