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Trial · NCT01574716

Results by group18

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

OutcomeGroupCategoryValueSpreadUnits
Part 2: Radiologic Progression-free Survival (PFS)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel18.795% Confidence Interval 11.6 to 27.4weeks
Part 2: Radiologic Progression-free Survival (PFS)Part 2: Placebo + Gemcitabine/Docetaxel24.195% Confidence Interval 11.1 to 36.1weeks
Part 2: Symptomatic Progression-free SurvivalPart 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel18.195% Confidence Interval 11.3 to 24.0weeks
Part 2: Symptomatic Progression-free SurvivalPart 2: Placebo + Gemcitabine/Docetaxel24.095% Confidence Interval 10.7 to 36.1weeks
Part 2: Overall Survival (OS)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel18.395% Confidence Interval 16.2 to 21.1months
Part 2: Overall Survival (OS)Part 2: Placebo + Gemcitabine/Docetaxel21.195% Confidence Interval 14.2 to NAmonths
Part 2: Overall Response Rate (ORR)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel19.4percentage of participants
Part 2: Overall Response Rate (ORR)Part 2: Placebo + Gemcitabine/Docetaxel20.0percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel12 weeks57.6percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: Placebo + Gemcitabine/Docetaxel12 weeks61.8percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel24 weeks43.3percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: Placebo + Gemcitabine/Docetaxel24 weeks51.0percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel48 weeks24.5percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: Placebo + Gemcitabine/Docetaxel48 weeks25.2percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel52 weeks20.8percentage of participants
Part 2: Radiologic Progression-free Survival Rate (PFR)Part 2: Placebo + Gemcitabine/Docetaxel52 weeks21.4percentage of participants
Part 2: Number of Participants Who Had Relationship Between MORAb-004 Exposures and Biomarker LevelsPart 2: MORAb-004 8.0 mg/kg + Gemcitabine/Docetaxel0participants
Part 2: Number of Participants Who Had Relationship Between MORAb-004 Exposures and Biomarker LevelsPart 2: Placebo + Gemcitabine/Docetaxel0participants

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.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01574716/results