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Trial · NCT03319940

Registered outcomes17

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of participants with dose limiting toxicities (DLT) for all indications6 months
PrimaryNumber of participants with treatment-emergent adverse events (AEs) for all indications4 years
PrimaryNumber of participants with treatment-related AEs for all indications4 years
PrimaryNumber of participants with clinically significant changes in vital signs for all indications4 years
PrimaryNumber of participants with significant changes in electrocardiogram (ECG) for all indications4 years
PrimaryNumber of participants with significant changes in physical examinations for all indications4 years
PrimaryNumber of participants with significant changes in clinical laboratory tests for all indications4 years
SecondaryMaximum observed concentration (Cmax) following intravenous administration for all indications4 years
SecondaryMinimum observed concentration (Cmin) following intravenous administration for all indications4 years
SecondaryArea under the concentration-time curve (AUC) over the 2 week dosing interval for all indications4 years
SecondaryAccumulation following multiple dosing for all indications4 years
SecondaryHalf-life (t1/2) following intravenous administration for all indications4 years
SecondaryObjective Response (OR) per modified Response Evaluation Criteria in Solid Tumors (RECIST) 1.14 yearsOnly for parts A, D, E, F, and G
SecondaryDuration of Response (DOR) for all indications4 years
SecondaryTime to Response (TTR)4 years
Secondary9-month Progression-Free Survival (PFS) for all indications9 months
Secondary9-month Overall Survival (OS) for all indications9 months

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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