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Trial · NCT04101331

Results by group30

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

OutcomeGroupCategoryValueSpreadUnits
Overall Response Rate Assessed by Independent Review Committee Based on PET-CTCohort A32.495% Confidence Interval 23.7 to 42.1percentage
Overall Response Rate Assessed by Investigator Based on PET-CTCohort A32.495% Confidence Interval 23.7 to 42.1percentage
Overall Response Rate Assessed by Investigator Based on CTCohort A30.695% Confidence Interval 22.1 to 40.2percentage
Complete Response Rate and Partial Response Rate Assessed by Independent Review Committee Based on PET-CTCohort AComplete response rate (CR rate)12.095% Confidence Interval 6.6 to 19.7percentage
Complete Response Rate and Partial Response Rate Assessed by Independent Review Committee Based on PET-CTCohort APartial response rate (PR rate)20.495% Confidence Interval 13.2 to 29.2percentage
Complete Response Rate, Partial Response Rate and Overall Response Rate Assessed by Independent Review Committee Based on CTCohort AOverall response rate (ORR)25.095% Confidence Interval 17.2 to 34.3percentage
Complete Response Rate, Partial Response Rate and Overall Response Rate Assessed by Independent Review Committee Based on CTCohort AComplete response rate (CR rate)7.495% Confidence Interval 3.3 to 14.1percentage
Complete Response Rate, Partial Response Rate and Overall Response Rate Assessed by Independent Review Committee Based on CTCohort APartial response rate (PR rate)17.695% Confidence Interval 10.9 to 26.1percentage
Duration of Overall Response Assessed by Independent Review Committee Based on PET-CTCohort A2.395% Confidence Interval 1.9 to 8.7months
Duration of Overall Response Assessed by Independent Review Committee Based on CTCohort A5.395% Confidence Interval 1.9 to 6.9months
Duration of Overall Response Assessed by Investigator Based on PET-CTCohort A3.395% Confidence Interval 1.9 to 8.7months
Duration of Overall Response Assessed by Investigator Based on CTCohort A6.395% Confidence Interval 2.0 to 8.7months
Number of Subjects With Treatment Related Adverse EventCohort A105Participants
Maximum Measured Concentration (Cmax) of AFM13Cohort ACycle 1 - day 126232Geometric Coefficient of Variation 270Nanogram/milliliter
Maximum Measured Concentration (Cmax) of AFM13Cohort ACycle 1 - day 2924435Geometric Coefficient of Variation 364Nanogram/milliliter
Area Under the Concentration-Time Curve of AFM13 From 0 to Infinity (AUC 0-∞)Cohort ACycle 1 - day 1612361Geometric Coefficient of Variation 60.3nanogram*hour/milliliter
Area Under the Concentration-Time Curve of AFM13 From 0 to Infinity (AUC 0-∞)Cohort ACycle 1 - day 29749717Geometric Coefficient of Variation 35nanogram*hour/milliliter
Volume of Distribution at Steady State (Vss) of AFM13Cohort A5.1Geometric Coefficient of Variation 58.4Liter
The Terminal Half-life (t1/2) of AFM13Cohort ACycle 1 - day 120.7Geometric Coefficient of Variation 35.9hour
The Terminal Half-life (t1/2) of AFM13Cohort ACycle 1 - day 2919.6Geometric Coefficient of Variation 47.4hour

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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