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Trial · NCT02606305

Results by group969

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Bevacizumab 15 mg/kgAny TEAE3Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + Bevacizumab 15 mg/kgAny TEAE126Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Carboplatin AUC4Any TEAE4Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Carboplatin AUC5Any TEAE4Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + Carboplatin AUC5Any TEAE10Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + PLD 30 mg/m^2Any TEAE4Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + PLD 40 mg/m^2Any TEAE4Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + PLD 40 mg/m^2Any TEAE7Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Pembrolizumab 200 mgAny TEAE4Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + Pembrolizumab 200 mgAny TEAE56Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine + Bevacizumab + CarboplatinAny TEAE41Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Bevacizumab 15 mg/kgSAEs2Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + Bevacizumab 15 mg/kgSAEs49Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Carboplatin AUC4SAEs2Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Carboplatin AUC5SAEs4Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + Carboplatin AUC5SAEs3Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + PLD 30 mg/m^2SAEs1Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + PLD 40 mg/m^2SAEs2Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 6 mg/kg + PLD 40 mg/m^2SAEs3Participants
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)Mirvetuximab Soravtansine 5 mg/kg + Pembrolizumab 200 mgSAEs2Participants

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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