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Trial · NCT02513550

Participant flow42

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Double Blind Treatment PeriodSTARTED80 mg Ixekizumab Q4W310
Double Blind Treatment PeriodSTARTED80 mg Ixekizumab Q4W/Q2W306
Double Blind Treatment PeriodSTARTED80 mg Ixekizumab Q2W611
Double Blind Treatment PeriodSTARTED80 mg Ixekizumab Q4W Maximum Extended Enrollment Cohort9
Double Blind Treatment PeriodSTARTED80 mg Ixekizumab Q4W/Q2W Maximum Extended Enrollment Cohort5
Double Blind Treatment PeriodSTARTED80 mg Ixekizumab Q2W Maximum Extended Enrollment Cohort16
Double Blind Treatment PeriodReceived at Least One Dose of Study Drug80 mg Ixekizumab Q4W310
Double Blind Treatment PeriodReceived at Least One Dose of Study Drug80 mg Ixekizumab Q4W/Q2W306
Double Blind Treatment PeriodReceived at Least One Dose of Study Drug80 mg Ixekizumab Q2W609
Double Blind Treatment PeriodReceived at Least One Dose of Study Drug80 mg Ixekizumab Q4W Maximum Extended Enrollment Cohort9
Double Blind Treatment PeriodReceived at Least One Dose of Study Drug80 mg Ixekizumab Q4W/Q2W Maximum Extended Enrollment Cohort5
Double Blind Treatment PeriodReceived at Least One Dose of Study Drug80 mg Ixekizumab Q2W Maximum Extended Enrollment Cohort16
Double Blind Treatment PeriodCOMPLETED80 mg Ixekizumab Q4W274
Double Blind Treatment PeriodCOMPLETED80 mg Ixekizumab Q4W/Q2W268
Double Blind Treatment PeriodCOMPLETED80 mg Ixekizumab Q2W537
Double Blind Treatment PeriodCOMPLETED80 mg Ixekizumab Q4W Maximum Extended Enrollment Cohort9
Double Blind Treatment PeriodCOMPLETED80 mg Ixekizumab Q4W/Q2W Maximum Extended Enrollment Cohort4
Double Blind Treatment PeriodCOMPLETED80 mg Ixekizumab Q2W Maximum Extended Enrollment Cohort15
Double Blind Treatment PeriodNOT COMPLETED80 mg Ixekizumab Q4W36
Double Blind Treatment PeriodNOT COMPLETED80 mg Ixekizumab Q4W/Q2W38

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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GET https://conductscience.org/api/trials/v1/NCT02513550/flow