ConductScience.org, home

Trial · NCT01930890

Results by group44

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 3 mg/kg (211LE202)Any event4participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 3 mg/kg (211LE201) to BIIB023 3 mg/kg (211LE202)Any event23participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 20 mg/kg (211LE202)Any event7participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 20 mg/kg (211LE201) to BIIB023 20 mg/kg (211LE202)Any event19participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 3 mg/kg (211LE202)Moderate or severe event2participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 3 mg/kg (211LE201) to BIIB023 3 mg/kg (211LE202)Moderate or severe event12participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 20 mg/kg (211LE202)Moderate or severe event3participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 20 mg/kg (211LE201) to BIIB023 20 mg/kg (211LE202)Moderate or severe event6participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 3 mg/kg (211LE202)Severe event0participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 3 mg/kg (211LE201) to BIIB023 3 mg/kg (211LE202)Severe event4participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 20 mg/kg (211LE202)Severe event1participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 20 mg/kg (211LE201) to BIIB023 20 mg/kg (211LE202)Severe event3participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 3 mg/kg (211LE202)Event related to dose-blinded treatment1participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 3 mg/kg (211LE201) to BIIB023 3 mg/kg (211LE202)Event related to dose-blinded treatment5participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 20 mg/kg (211LE202)Event related to dose-blinded treatment1participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 20 mg/kg (211LE201) to BIIB023 20 mg/kg (211LE202)Event related to dose-blinded treatment4participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 3 mg/kg (211LE202)Event related to MMF2participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 3 mg/kg (211LE201) to BIIB023 3 mg/kg (211LE202)Event related to MMF8participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)Placebo (211LE201) to BIIB023 20 mg/kg (211LE202)Event related to MMF2participants
Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)BIIB023 20 mg/kg (211LE201) to BIIB023 20 mg/kg (211LE202)Event related to MMF9participants

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/NCT01930890/results