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Trial · NCT01137006

Results by group29

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

OutcomeGroupCategoryValueSpreadUnits
Maximum Tolerated Dose (MTD) of IMC-20D7SIMC-20D7S20mg/kg q2w
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 1A (5 mg/kg, q2w)SAEs1participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 2A (10 mg/kg, q2w)SAEs1participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 3A (20 mg/kg, q2w)SAEs5participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 4A (30 mg/kg, q2w)SAEs2participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 1B (10 mg/kg, q3w)SAEs0participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 2B (20 mg/kg, q3w)SAEs4participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 3B (30 mg/kg, q3w)SAEs0participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 1A (5 mg/kg, q2w)Other Non-Serious AEs3participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 2A (10 mg/kg, q2w)Other Non-Serious AEs3participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 3A (20 mg/kg, q2w)Other Non-Serious AEs8participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 4A (30 mg/kg, q2w)Other Non-Serious AEs3participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 1B (10 mg/kg, q3w)Other Non-Serious AEs2participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 2B (20 mg/kg, q3w)Other Non-Serious AEs4participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 3B (30 mg/kg, q3w)Other Non-Serious AEs3participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 1A (5 mg/kg, q2w)Deaths0participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 2A (10 mg/kg, q2w)Deaths0participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 3A (20 mg/kg, q2w)Deaths0participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 4A (30 mg/kg, q2w)Deaths0participants
Number of Participants With Serious Adverse Events (SAEs), Other Non-Serious Adverse Events (AEs), or DeathCohort 1B (10 mg/kg, q3w)Deaths0participants

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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