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Trial · NCT04297995

Registered outcomes13

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

ListOutcomeTime frameDescription
PrimaryPart1: Efficacy-ORRat 16 weeks after first doseObjective Response Rate (ORR)
PrimaryPart1: Safety-adverse event profileup to one yearThe proportion of patients suffered from drug related toxicities.
PrimaryPart2: Efficacy-ORR (IRRC)at 3 months after first doseObjective Response Rate (ORR) assessed by the Independent Radiological Review Committee (IRRC) per RECIST v1.1.
SecondaryEfficacy-Best ORRup to one yearBest response rate (Best ORR)
SecondaryEfficacy-PFSup to one yearProgression-free survival (PFS)
SecondaryEfficacy-OSup to one yearOverall survival (OS)
SecondaryThe number of presence patients that develop of anti-durg antibody (immunogenicity).up to one year
Secondarymaximum concentration (Cmax)up to one year
Secondarytrough concentration (Ctrough)up to one year
Secondaryhalf-life (T1/2)up to one year
Secondaryclearance rate (CL)up to one year
Secondaryvolume of distribution (Vss)up to one year
Secondaryarea under concentration (AUC0-tau)up to one year

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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GET https://conductscience.org/api/trials/v1/NCT04297995/registered