Treatment of participants with positive cancer for HRRm or HRD.
Conditions
Brief summary
Objective Response Rate (ORR)
Detailed description
Duration of Response (DOR), Overall Survival (OS), Progression Free Survival (PFS), Number of Participants Experiencing an Adverse Event (AE), Number of Participants Discontinuing Study Treatment due to an Adverse Event (AE), Objective Response Rate (ORR) in Participants with HRRm or HRD Positive Cancer, Time to Earliest Progression by Cancer Antigen-125 (CA-125), Prostate-specific Antigen (PSA) Response Rate in Participants with Prostate Cancer, Progression-Free Survival After Next-Line Treatment in Participants with sBRCAm Breast Cancer
Interventions
Sponsors
Eligibility
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Objective Response Rate (ORR) | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of Response (DOR), Overall Survival (OS), Progression Free Survival (PFS), Number of Participants Experiencing an Adverse Event (AE), Number of Participants Discontinuing Study Treatment due to an Adverse Event (AE), Objective Response Rate (ORR) in Participants with HRRm or HRD Positive Cancer, Time to Earliest Progression by Cancer Antigen-125 (CA-125), Prostate-specific Antigen (PSA) Response Rate in Participants with Prostate Cancer, Progression-Free Survival After Next-Line Treatment in Participants with sBRCAm Breast Cancer | — |
Countries
Denmark, France, Ireland, Italy, Romania, Spain