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Trial · NCT05208866

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Who Develop Serum ALT Levels >3 × ULN During the Lixivaptan Re-titration or Maintenance Treatment Periods Assessed to be Related to Lixivaptan and Resulted in Discontinuation of Lixivaptan Treatment
All Enrolled Participants0Participants
Number of Participants Who Develop Serum ALT Levels >5 x ULN During the Lixivaptan Re-titration or Maintenance Treatment Periods Assessed to be Related to Lixivaptan and Resulted in Discontinuation of Lixivaptan Treatment
All Enrolled Participants0Participants
Number of Participants Who Develop Serum ALT Values >3 × ULN During the Lixivaptan Re-titration or Maintenance Treatment Periods Assessed to be Related to Lixivaptan and Resulted in Dose Reduction of Lixivaptan Treatment
All Enrolled Participants0Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs)All Enrolled ParticipantsLixivaptan Re-titration and Maintenance Treatment Periods1Participants
Number of Participants With Treatment-emergent Adverse Events (TEAEs)All Enrolled ParticipantsFollow-up Period0Participants
Number of Participants With Potentially Clinically Important Clinical Laboratory FindingsAll Enrolled ParticipantsLixivaptan Re-titration and Maintenance Treatment Periods0Participants
Number of Participants With Potentially Clinically Important Clinical Laboratory FindingsAll Enrolled ParticipantsFollow-up Period0Participants
Number of Participants With Potentially Clinically Important Vital Signs FindingsAll Enrolled ParticipantsLixivaptan Re-titration and Maintenance Treatment Periods0Participants
Number of Participants With Potentially Clinically Important Vital Signs FindingsAll Enrolled ParticipantsFollow-up Period0Participants
Number of Participants With Potentially Clinically Important 12-lead Electrocardiogram (ECG) FindingsAll Enrolled ParticipantsLixivaptan Re-titration and Maintenance Treatment Periods0Participants
Number of Participants With Potentially Clinically Important 12-lead Electrocardiogram (ECG) FindingsAll Enrolled ParticipantsFollow-up Period0Participants
Annualized Change in Estimated Glomerular Filtration Rate (eGFR) From Baseline to Final AssessmentAll Enrolled Participants14.6Standard Deviation 0.0mL/min/1.73m^2

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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