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Trial · NCT00726232

Participant flow80

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

PeriodMilestoneGroupParticipantsUnits counted
Initial Phase (Dose-finding)STARTEDPolycythemia Vera (PV): Ruxolitinib 10 mg BID19
Initial Phase (Dose-finding)STARTEDPV: Ruxolitinib 25 mg BID8
Initial Phase (Dose-finding)STARTEDPV: Ruxolitinib 50 mg QD7
Initial Phase (Dose-finding)STARTEDEssential Thrombocythemia (ET): Ruxolitinib 10 mg BID8
Initial Phase (Dose-finding)STARTEDET: Ruxolitinib 25 mg BID22
Initial Phase (Dose-finding)STARTEDET: Ruxolitinib 50 mg QD9
Initial Phase (Dose-finding)STARTEDPV: Ruxolitinib All Doses Combined- Expansion Phase0
Initial Phase (Dose-finding)STARTEDET: Ruxolitinib All Doses Combined-expansion Phase0
Initial Phase (Dose-finding)Safety Evaluable ParticipantsPolycythemia Vera (PV): Ruxolitinib 10 mg BID19
Initial Phase (Dose-finding)Safety Evaluable ParticipantsPV: Ruxolitinib 25 mg BID8
Initial Phase (Dose-finding)Safety Evaluable ParticipantsPV: Ruxolitinib 50 mg QD7
Initial Phase (Dose-finding)Safety Evaluable ParticipantsEssential Thrombocythemia (ET): Ruxolitinib 10 mg BID8
Initial Phase (Dose-finding)Safety Evaluable ParticipantsET: Ruxolitinib 25 mg BID22
Initial Phase (Dose-finding)Safety Evaluable ParticipantsET: Ruxolitinib 50 mg QD9
Initial Phase (Dose-finding)Safety Evaluable ParticipantsPV: Ruxolitinib All Doses Combined- Expansion Phase0
Initial Phase (Dose-finding)Safety Evaluable ParticipantsET: Ruxolitinib All Doses Combined-expansion Phase0
Initial Phase (Dose-finding)ITT ParticipantsPolycythemia Vera (PV): Ruxolitinib 10 mg BID19
Initial Phase (Dose-finding)ITT ParticipantsPV: Ruxolitinib 25 mg BID8
Initial Phase (Dose-finding)ITT ParticipantsPV: Ruxolitinib 50 mg QD7
Initial Phase (Dose-finding)ITT ParticipantsEssential Thrombocythemia (ET): Ruxolitinib 10 mg BID8

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/NCT00726232/flow