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Trial · NCT03150056

Results by group430

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg+Abiraterone 1000 mgAny AEs10Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg Alternate+Abiraterone 1000 mgAny AEs6Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 40 mg+Abiraterone 1000 mgAny AEs4Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 80 mg+Enzalutamide 160 mgAny AEs10Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg+Enzalutamide 160 mgAny AEs22Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg Alternate+Enzalutamide 160 mgAny AEs21Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg+Abiraterone 1000 mgAny SAEs4Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg Alternate+Abiraterone 1000 mgAny SAEs2Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 40 mg+Abiraterone 1000 mgAny SAEs0Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 80 mg+Enzalutamide 160 mgAny SAEs1Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg+Enzalutamide 160 mgAny SAEs6Participants
Number of Participants With Any Adverse Events (AEs) and Serious Adverse Events (SAEs)GSK525762 60 mg Alternate+Enzalutamide 160 mgAny SAEs7Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 60 mg+Abiraterone 1000 mgDose reduction4Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 60 mg Alternate+Abiraterone 1000 mgDose reduction1Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 40 mg+Abiraterone 1000 mgDose reduction0Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 80 mg+Enzalutamide 160 mgDose reduction7Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 60 mg+Enzalutamide 160 mgDose reduction10Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 60 mg Alternate+Enzalutamide 160 mgDose reduction7Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 60 mg+Abiraterone 1000 mgDose delay5Participants
Number of Participants With AEs Leading to Any Dose Reduction or DelaysGSK525762 60 mg Alternate+Abiraterone 1000 mgDose delay2Participants

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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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03150056/results