ConductScience.org, home

Trial · NCT03226678

Results by group108

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

OutcomeGroupCategoryValueSpreadUnits
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 270 mgAll TEAEs5Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 360 mgAll TEAEs5Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 2 CAD - 270 mgAll TEAEs7Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 2 CAD - 360 mgAll TEAEs6Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart B: Cohort 1 wAIHA - 1080 mgAll TEAEs5Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart B: Cohort 2 CAD - 1080 mgAll TEAEs9Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 270 mgTreatment related TEAEs4Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 360 mgTreatment related TEAEs4Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 2 CAD - 270 mgTreatment related TEAEs5Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 2 CAD - 360 mgTreatment related TEAEs4Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart B: Cohort 1 wAIHA - 1080 mgTreatment related TEAEs4Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart B: Cohort 2 CAD - 1080 mgTreatment related TEAEs5Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 270 mgSerious AEs3Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 360 mgSerious AEs2Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 2 CAD - 270 mgSerious AEs3Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 2 CAD - 360 mgSerious AEs2Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart B: Cohort 1 wAIHA - 1080 mgSerious AEs2Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart B: Cohort 2 CAD - 1080 mgSerious AEs6Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 270 mgTEAEs leading to study drug discontinuation1Participants
Number of Subjects With Treatment Emergent Adverse Events (TEAEs) Including by SeverityPart A: Cohort 1 wAIHA - 360 mgTEAEs leading to study drug discontinuation2Participants

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

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03226678/results