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Trial · NCT01360840

Results by group65

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

OutcomeGroupCategoryValueSpreadUnits
Progression Free Survival (PFS) TimePlacebo + SoC3.395% Confidence Interval 2.8 to 4.8months
Progression Free Survival (PFS) TimeEMD 525797 750 mg + SoC3.495% Confidence Interval 2.8 to 5.6months
Progression Free Survival (PFS) TimeEMD 525797 1500 mg + SoC4.395% Confidence Interval 2.8 to 6.6months
Overall SurvivalPlacebo + SoCNA95% Confidence Interval 14.8 to NAmonths
Overall SurvivalEMD 525797 750 mg + SoCNA95% Confidence Interval 12.9 to NAmonths
Overall SurvivalEMD 525797 1500 mg + SoCNA95% Confidence Interval 14.4 to NAmonths
Time to Tumor ProgressionPlacebo + SoC3.395% Confidence Interval 2.8 to 5.4months
Time to Tumor ProgressionEMD 525797 750 mg + SoC3.495% Confidence Interval 2.8 to 5.6months
Time to Tumor ProgressionEMD 525797 1500 mg + SoC4.695% Confidence Interval 2.8 to 6.9months
Number of Subjects With Presence of Tumor Response and Disease Control (DC) in Soft Tissue LesionsPlacebo + SoCTumor response1Subjects
Number of Subjects With Presence of Tumor Response and Disease Control (DC) in Soft Tissue LesionsEMD 525797 750 mg + SoCTumor response0Subjects
Number of Subjects With Presence of Tumor Response and Disease Control (DC) in Soft Tissue LesionsEMD 525797 1500 mg + SoCTumor response1Subjects
Number of Subjects With Presence of Tumor Response and Disease Control (DC) in Soft Tissue LesionsPlacebo + SoCDisease control2Subjects
Number of Subjects With Presence of Tumor Response and Disease Control (DC) in Soft Tissue LesionsEMD 525797 750 mg + SoCDisease control3Subjects
Number of Subjects With Presence of Tumor Response and Disease Control (DC) in Soft Tissue LesionsEMD 525797 1500 mg + SoCDisease control4Subjects
Number of Subjects With New Bone Lesions Compared to BaselinePlacebo + SoC40Subjects
Number of Subjects With New Bone Lesions Compared to BaselineEMD 525797 750 mg + SoC34Subjects
Number of Subjects With New Bone Lesions Compared to BaselineEMD 525797 1500 mg + SoC34Subjects
Number of Subjects With Presence of DC in Bone LesionsPlacebo + SoCWeek 134Subjects
Number of Subjects With Presence of DC in Bone LesionsEMD 525797 750 mg + SoCWeek 137Subjects

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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