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Trial · NCT02697630

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryObjective Response Rate (ORR)From first dose up to 24 monthsThe proportion of patients that have a best overall response of complete response (CR) or partial response (PR), as assessed by RECIST 1.1.
SecondaryClinical benefit rate (CBR)18 weeks from first dose
SecondaryProgression free survival (PFS)From first dose up to 24 months
SecondaryOverall Survival (OS)From first dose up to 24 months
SecondaryBest overall response (BOR)From first dose up to 24 months
SecondaryTime To Response (TTR)From first dose up to 24 months
SecondaryDuration of objective response (DOR)From first dose up to 24 months
SecondaryAdverse Events (AEs) and Serious Adverse Events (SAEs).From first dose up to 24 monthsIncidence and severity
SecondaryEastern Cooperative Oncology Group (ECOG) Performance status (PS)18 weeks from first dose
SecondaryQuality of Life (QoL) assessed by FACT-GFrom first dose up to 24 months
SecondaryQuality of Life (QoL) assessed by EQ5D-3LFrom first dose up to 24 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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GET https://conductscience.org/api/trials/v1/NCT02697630/registered