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Trial · NCT05361655

Results by group31

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

OutcomeGroupCategoryValueSpreadUnits
Overall Survival (OS) in Postmenopausal Female or Male Participants With Metastatic Breast CancerPalbociclib + Aromatase Inhibitor49.195% Confidence Interval 45.2 to 57.7Months
Overall Survival (OS) in Postmenopausal Female or Male Participants With Metastatic Breast CancerAromatase Inhibitor43.295% Confidence Interval 37.6 to 48.0Months
Real-World Progression Free Survival (rwPFS) in Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase Inhibitor19.395% Confidence Interval 17.5 to 20.7Months
Real-World Progression Free Survival (rwPFS) in Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase Inhibitor13.995% Confidence Interval 12.5 to 15.2Months
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase InhibitorComplete response163Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase InhibitorComplete response86Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase InhibitorPartial response569Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase InhibitorPartial response300Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase InhibitorStable disease350Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase InhibitorStable disease273Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase InhibitorProgressive disease155Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase InhibitorProgressive disease260Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase InhibitorIndeterminate response26Participants
Number of Participants According to Real-World Tumor Responses (rwTR): Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase InhibitorIndeterminate response69Participants
Real-World Response Rate (rwTR) in Postmenopausal Female or in Male Participants With Metastatic Breast CancerPalbociclib + Aromatase Inhibitor57.98Percentage of participants
Real-World Response Rate (rwTR) in Postmenopausal Female or in Male Participants With Metastatic Breast CancerAromatase Inhibitor39.04Percentage of participants
Number of Participants According to Initial Dose of Palbociclib: Palbociclib + Aromatase Inhibitor Arm OnlyPalbociclib + Aromatase InhibitorPalbociclib 75 mg/day48Participants
Number of Participants According to Initial Dose of Palbociclib: Palbociclib + Aromatase Inhibitor Arm OnlyPalbociclib + Aromatase InhibitorPalbociclib 125 mg/day1110Participants
Number of Participants According to Initial Dose of Palbociclib: Palbociclib + Aromatase Inhibitor Arm OnlyPalbociclib + Aromatase InhibitorPalbociclib 100 mg/day144Participants
Number of Participants According to Initial Dose of Palbociclib: Palbociclib + Aromatase Inhibitor Arm OnlyPalbociclib + Aromatase InhibitorMissing22Participants

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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