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Trial · NCT02603172

Participant flow72

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

PeriodMilestoneGroupParticipantsUnits counted
Part A (Approximately 16 Weeks)STARTEDGSK3039294 200 mg + GSK3039294 600 mg7
Part A (Approximately 16 Weeks)STARTEDGSK3039294 200 mg + GSK3039294 600 mg/GSK3039294 600 mg QD1
Part A (Approximately 16 Weeks)STARTEDGSK3039294 600 mg +GSK3039294 1200 mg8
Part A (Approximately 16 Weeks)STARTEDGSK3039294 600 mg +GSK3039294 1200 mg/GSK3039294 600 mg QD1
Part A (Approximately 16 Weeks)STARTEDGSK3039294 600 mg QD0
Part A (Approximately 16 Weeks)STARTEDGSK3039294 (Cohort 4a)0
Part A (Approximately 16 Weeks)STARTEDGSK3039294 (Cohort 4b)0
Part A (Approximately 16 Weeks)STARTEDPart C: GSK30392940
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 200 mg + GSK3039294 600 mg7
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 200 mg + GSK3039294 600 mg/GSK3039294 600 mg QD1
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 600 mg +GSK3039294 1200 mg7
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 600 mg +GSK3039294 1200 mg/GSK3039294 600 mg QD1
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 600 mg QD0
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 (Cohort 4a)0
Part A (Approximately 16 Weeks)COMPLETEDGSK3039294 (Cohort 4b)0
Part A (Approximately 16 Weeks)COMPLETEDPart C: GSK30392940
Part A (Approximately 16 Weeks)NOT COMPLETEDGSK3039294 200 mg + GSK3039294 600 mg0
Part A (Approximately 16 Weeks)NOT COMPLETEDGSK3039294 200 mg + GSK3039294 600 mg/GSK3039294 600 mg QD0
Part A (Approximately 16 Weeks)NOT COMPLETEDGSK3039294 600 mg +GSK3039294 1200 mg1
Part A (Approximately 16 Weeks)NOT COMPLETEDGSK3039294 600 mg +GSK3039294 1200 mg/GSK3039294 600 mg QD0

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/NCT02603172/flow