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Trial · NCT02723955

Results by group19,265

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

1 to 20 of 19,265Pages stop at row 10,000

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OutcomeGroupCategoryValueSpreadUnits
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Feladilimab (Fela) 0.001 Milligram/Kilogram (mg/kg)Any AEs1Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.003 mg/kgAny AEs1Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.010 mg/kgAny AEs2Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.030 mg/kgAny AEs7Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.100 mg/kgAny AEs22Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.300 mg/kgAny AEs24Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 1.000 mg/kgAny AEs13Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 3.000 mg/kgAny AEs21Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 10.000 mg/kgAny AEs6Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Feladilimab (Fela) 0.001 Milligram/Kilogram (mg/kg)Any SAEs0Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.003 mg/kgAny SAEs0Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.010 mg/kgAny SAEs1Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.030 mg/kgAny SAEs2Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.100 mg/kgAny SAEs6Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 0.300 mg/kgAny SAEs8Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 1.000 mg/kgAny SAEs4Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 3.000 mg/kgAny SAEs12Participants
Part 1A: Number of Participants With Any Adverse Event(s) (AEs) and Serious Adverse Event(s) (SAEs)Part 1A: Fela 10.000 mg/kgAny SAEs1Participants
Part 1A: Number of Participants With Dose Limiting Toxicity (DLT)Part 1A: Feladilimab (Fela) 0.001 Milligram/Kilogram (mg/kg)0Participants
Part 1A: Number of Participants With Dose Limiting Toxicity (DLT)Part 1A: Fela 0.003 mg/kg0Participants

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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