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Trial · NCT05460325

Results by group67

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)Lanadelumab 300 mgTEAEs: Non-Angioedema Attack15Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)Lanadelumab 300 mgTEAEs: Angioedema Attack3Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)Lanadelumab 300 mgSAEs: Non-Angioedema Attack1Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)Lanadelumab 300 mgSAEs: Angioedema Attack0Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)Lanadelumab 300 mgAESIs: Non-Angioedema Attack0Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)Lanadelumab 300 mgAESIs: Angioedema Attack0Participants
Number of Participants With Clinically Meaningful Changes in Clinical Laboratory ParametersLanadelumab 300 mg0Participants
Number of Participants With Clinically Meaningful Changes in Vital Sign AbnormalitiesLanadelumab 300 mg0Participants
Number of Participants With Clinically Meaningful Changes in Electrocardiogram (ECG)Lanadelumab 300 mg0Participants
Number of Participants With Clinically Significant Physical Examination Abnormalities on Day 182Lanadelumab 300 mgDermatologic System2Participants
Number of Participants With Clinically Significant Physical Examination Abnormalities on Day 182Lanadelumab 300 mgExtremities1Participants
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 07.64Standard Deviation 24.096nanograms per milliliter (ng/mL)
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 14: Pre-dose12336.47Standard Deviation 4531.386nanograms per milliliter (ng/mL)
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 56: Pre-dose24857.89Standard Deviation 6950.725nanograms per milliliter (ng/mL)
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 98: Pre-dose24170.00Standard Deviation 7260.426nanograms per milliliter (ng/mL)
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 140: Pre-dose23821.05Standard Deviation 8808.870nanograms per milliliter (ng/mL)
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 182: Pre-dose24610.00Standard Deviation 6599.673nanograms per milliliter (ng/mL)
Plasma Concentrations of LanadelumabLanadelumab 300 mgDay 21012048.00Standard Deviation 3268.807nanograms per milliliter (ng/mL)
Plasma Kallikrein (pKal) ActivityLanadelumab 300 mgDay 010256.419Standard Deviation 3311.3810ng/mL
Plasma Kallikrein (pKal) ActivityLanadelumab 300 mgDay 14: Pre-dose4904.964Standard Deviation 1350.4121ng/mL

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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