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Trial · NCT03398148

Adverse events1,305

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 1: Double-blind Placebo IV2592
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 1: Double-blind Risankizumab 600mg IV0620
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 1: Double-blind Risankizumab 1200mg IV2613
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 1: Double-blind Risankizumab 1800mg IV1581
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 1: Openlabel Risankizumab 1800mg IV1234112
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 2: Double-blind Risankizumab 1800mg IV Pbo0360
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 2: Double-blind Risankizumab 1800mg IV1371
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 2: Double-blind Risankizumab 180mg SC1711
otherANAEMIABlood and lymphatic system disordersSubstudy 1, Induction Period 2: Double-blind Risankizumab 360mg SC1711
otherANAEMIABlood and lymphatic system disordersSubstudy 2, Induction Period 1: Double-blind Placebo IV1932421
otherANAEMIABlood and lymphatic system disordersSubstudy 2, Induction Period 1: Double-blind Risankizumab 1200mg IV2165321
otherANAEMIABlood and lymphatic system disordersSubstudy 2, Induction Period 2: Double-blind Risankizumab 1200mg IV Pbo51745
otherANAEMIABlood and lymphatic system disordersSubstudy 2, Induction Period 2: Double-blind Risankizumab 1200mg IV1681
otherANAEMIABlood and lymphatic system disordersSubstudy 2, Induction Period 2: Double-blind Risankizumab 180mg SC2712
otherANAEMIABlood and lymphatic system disordersSubstudy 2, Induction Period 2: Double-blind Risankizumab 360mg SC6716
otherCOLITIS ULCERATIVEGastrointestinal disordersSubstudy 1, Induction Period 1: Double-blind Placebo IV5596
otherCOLITIS ULCERATIVEGastrointestinal disordersSubstudy 1, Induction Period 1: Double-blind Risankizumab 600mg IV1621
otherCOLITIS ULCERATIVEGastrointestinal disordersSubstudy 1, Induction Period 1: Double-blind Risankizumab 1200mg IV3613
otherCOLITIS ULCERATIVEGastrointestinal disordersSubstudy 1, Induction Period 1: Double-blind Risankizumab 1800mg IV1581
otherCOLITIS ULCERATIVEGastrointestinal disordersSubstudy 1, Induction Period 1: Openlabel Risankizumab 1800mg IV1234112

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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