Efficacy and Safety of the Combination of Rucaparib (PARP Inhibitor) and Atezolizumab (Anti-PD-L1 Antibody) in Patients With DNA Repair-deficient or Platinum-sensitive Solid Tumors
- Registration Number
- NCT04276376
- Lead Sponsor
- Gustave Roussy, Cancer Campus, Grand Paris
- Brief Summary
The primary objective of the trial is to evaluate the antitumor activity of atezolizumab and rucaparib in patients with selected advanced solid tumors as measured by the Overall Response Rate
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- SUSPENDED
- Sex
- All
- Target Recruitment
- 130
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cohort 1A-D Atezolizumab Molecularly selected cohorts that harbor DNA repair deficiency, defined as bi-allelic loss-of-function alteration (mutation and/or deletion) in at least one of the following genes: ATM, BARD1, BRCA1, BRCA2, BRIP1, CDK12, CHEK2, PALB2, RAD51C, RAD51D, FANCA, NBN, RAD51, RAD54L. 1.A - Non-Small Cell Lung Cancer 1.B - Urothelial Bladder Cancer 1.C - metastatic Castration Resistant Prostate Cancer 1.D - others: any histology, excepted breast cancer or serous ovarian cancer Cohort 4 Atezolizumab Clear Cell Renal Cell Carcinoma Cohort 2A-C Atezolizumab Platinum-sensitive disease 2.A - Non-Small Cell Lung Cancer 2.B - Urothelial Bladder Cancer 2.C - Gastric or gastro-esophageal junction adenocarcinoma Cohort 1A-D Rucaparib Molecularly selected cohorts that harbor DNA repair deficiency, defined as bi-allelic loss-of-function alteration (mutation and/or deletion) in at least one of the following genes: ATM, BARD1, BRCA1, BRCA2, BRIP1, CDK12, CHEK2, PALB2, RAD51C, RAD51D, FANCA, NBN, RAD51, RAD54L. 1.A - Non-Small Cell Lung Cancer 1.B - Urothelial Bladder Cancer 1.C - metastatic Castration Resistant Prostate Cancer 1.D - others: any histology, excepted breast cancer or serous ovarian cancer Cohort 3 Rucaparib Metastatic Castration Resistant Prostate Cancer (mCRPC) Cohort 4 Rucaparib Clear Cell Renal Cell Carcinoma Cohort 2A-C Rucaparib Platinum-sensitive disease 2.A - Non-Small Cell Lung Cancer 2.B - Urothelial Bladder Cancer 2.C - Gastric or gastro-esophageal junction adenocarcinoma Cohort 3 Atezolizumab Metastatic Castration Resistant Prostate Cancer (mCRPC)
- Primary Outcome Measures
Name Time Method Overall Response Rate at 12 weeks
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the synergy of PARP inhibition and PD-L1 blockade in DNA repair-deficient tumors?
How does the rucaparib and atezolizumab combination compare to standard-of-care therapies in platinum-sensitive solid tumors?
Which biomarkers are most predictive of response to PARP and PD-L1 dual inhibition in advanced solid cancers?
What are the most common adverse events associated with rucaparib-atezolizumab combination therapy and their management strategies?
Are there alternative DNA repair-targeting agents being tested with anti-PD-L1 antibodies in similar tumor subtypes?
Trial Locations
- Locations (1)
Gustave Roussy
🇫🇷Villejuif, Val De Marne, France
Gustave Roussy🇫🇷Villejuif, Val De Marne, France