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Trial · NCT01609556

Participant flow112

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

PeriodMilestoneGroupParticipantsUnits counted
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule A (Mirvetuximab Soravtansine 3.3 mg/kg Q3W)9
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule A (Mirvetuximab Soravtansine 5.0 mg/kg Q3W)18
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule A (Mirvetuximab Soravtansine 6.0 mg/kg Q3W)7
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule A (Mirvetuximab Soravtansine 7.0 mg/kg Q3W)5
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule B (Mirvetuximab Soravtansine 1.1 mg/kg Weekly)5
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule B (Mirvetuximab Soravtansine 1.8 mg/kg Weekly)4
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule B (Mirvetuximab Soravtansine 2.0 mg/kg Weekly)9
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Escalation: Schedule B (Mirvetuximab Soravtansine 2.5 mg/kg Weekly)7
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Expansion: Cohort 1 (Mirvetuximab Soravtansine Q3W)0
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Expansion: Cohort 2 (Mirvetuximab Soravtansine Q3W)0
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Expansion: Cohort 3 (Mirvetuximab Soravtansine Q3W)0
Dose Escalation: Maximum 101.3 WeeksReceived at Least 1 Dose of Study DrugDose Expansion: Cohort 5 (Mirvetuximab Soravtansine Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 0.15 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 0.5 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 1.0 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 2.0 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 3.3 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 5.0 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 6.0 mg/kg Q3W)0
Dose Escalation: Maximum 101.3 WeeksCOMPLETEDDose Escalation: Schedule A (Mirvetuximab Soravtansine 7.0 mg/kg Q3W)0

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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