Clinical trial
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Phase
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Study objective
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Germline mutations
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Somatic mutations
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Outcomes
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Olaparib with chemotherapy and targeted therapy
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NCT00515866 [36]
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Phase I
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Evaluate the safety and MTD of olaparib with gemcitabine versus gemcitabine alone in patients with locally advanced/metastatic pancreatic cancer
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Unselected for mutations
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Out of 66 patients treated, olaparib 100 mg twice daily with gemcitabine 600 mg/m2 was the most tolerable combination.
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NCT01296763 [37]
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phase I
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Dose escalation trial evaluating olaparib in combination with irinotecan, cisplatin, and mitomycin C in patients with advanced pancreatic cancer
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Known BRCA-mutated or Jewish ancestry patients and those with familial and sporadic pancreatic cancer were included
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Early closure due to toxicity
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NCT03682289 [38]
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phase II
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Studying the efficacy of ATR kinase inhibitor AZD6738 alone versus combination with olaparib in patients with advanced renal cell, urothelial and pancreatic cancers
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N/A
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BAF250a-positive received AZD6738 with olaparib and BAF250a-negative or ATM-mutant received AZD6738 only
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Currently recruiting
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NCT02498613 [39]
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Phase II
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Study evaluating cediranib maleate combined with olaparib in advanced breast, non-small-cell and small-cell lung cancer, and pancreatic cancer patients
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Identification of DNA repair genes in tumors using the BROCA panel with a plan to correlate tumor regression with mutations status
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Currently recruiting
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NCT03205176 [40]
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Phase I
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Study evaluating MTD and preliminary antitumor activity of AZD5153 in relapsed/refractory malignant solid tumor, including lymphoma patients as a single agent or in combination with olaparib.
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Patients are included regardless of BRCA status. Planned to collect BRCA and HRD gene mutational status
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Currently recruiting
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NCT04005690 [41]
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Phase II window of opportunity trial
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Evaluating cobimetinib or olaparib response in patients with resectable pancreatic cancer by comparing pretreatment biopsy samples with posttreatment resection specimens
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N/A
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Currently recruiting
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Olaparib with immunotherapy
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NCT03851614 (DAPPER) [42]
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Phase II
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Evaluating changes in genomic and immune biomarkers in tumor, peripheral blood, and stool; changes in radiomic profiles, with the combination of durvalumab with olaparib or cediranib
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Patients with germline or somatic DDR genes will be evaluated retrospectively but is not an eligibility criteria
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Currently recruiting
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