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Trial · NCT04603495

Participant flow22

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPelabresib + Ruxolitinib (Experimental Arm)214
Overall StudySTARTEDPlacebo + Ruxolitinib (Control Arm)216
Overall StudyModified Intent-to-Treat (mITT) Analysis SetPelabresib + Ruxolitinib (Experimental Arm)212
Overall StudyModified Intent-to-Treat (mITT) Analysis SetPlacebo + Ruxolitinib (Control Arm)214
Overall StudySafety Analysis SetPelabresib + Ruxolitinib (Experimental Arm)212
Overall StudySafety Analysis SetPlacebo + Ruxolitinib (Control Arm)214
Overall StudyPer-Protocol Set (PP Set)Pelabresib + Ruxolitinib (Experimental Arm)196
Overall StudyPer-Protocol Set (PP Set)Placebo + Ruxolitinib (Control Arm)194
Overall StudyPharmacokinetic (PK) Analysis SetPelabresib + Ruxolitinib (Experimental Arm)212
Overall StudyPharmacokinetic (PK) Analysis SetPlacebo + Ruxolitinib (Control Arm)211
Overall StudyBiomarker Analysis SetPelabresib + Ruxolitinib (Experimental Arm)212
Overall StudyBiomarker Analysis SetPlacebo + Ruxolitinib (Control Arm)214
Overall StudyOngoing on Double-blind TreatmentPelabresib + Ruxolitinib (Experimental Arm)154
Overall StudyOngoing on Double-blind TreatmentPlacebo + Ruxolitinib (Control Arm)160
Overall StudyDiscontinued Double-blind TreatmentPelabresib + Ruxolitinib (Experimental Arm)58
Overall StudyDiscontinued Double-blind TreatmentPlacebo + Ruxolitinib (Control Arm)54
Overall StudyOn PFS/OS Follow-upPelabresib + Ruxolitinib (Experimental Arm)22
Overall StudyOn PFS/OS Follow-upPlacebo + Ruxolitinib (Control Arm)30
Overall StudyCOMPLETEDPelabresib + Ruxolitinib (Experimental Arm)181
Overall StudyCOMPLETEDPlacebo + Ruxolitinib (Control Arm)193

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/NCT04603495/flow