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Study identifier: NCT07667751 Synced from ClinicalTrials.gov · July 29, 2026
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An Exploratory Study on the Use of Ipalotinib (Tislelizumab) Combined With Sunitinib and Olaparib for Neoadjuvant Therapy in HRD-positive Advanced Ovarian Cancer

Condition: Ovary Cancer  ·  Sponsor: Bai-Rong Xia

PhasePhase 2
Planned participants35
Who can joinFemale, 18 Years to 75 Years
Healthy volunteersNo

About this study

The R0 resection rate in neoadjuvant chemotherapy for advanced ovarian cancer remains below 50%, indicating unmet clinical needs. Tyrosine kinase inhibitors (TKIs) can induce immune microenvironment remodeling and exhibit synergistic effects with immune checkpoint inhibitors. To further evaluate the efficacy and safety of epalolide combined with torvolumab plus sunitinib and olaparib as neoadjuvant therapy in HRD-positive untreated patients with advanced ovarian cancer, a prospective, multicenter, single-arm exploratory study is proposed. This study will enroll 35 untreated HRD-positive advanced ovarian cancer patients who will receive neoadjuvant treatment with epalolide plus torvolumab combined with sunitinib and olaparib. Patients achieving CR/PR/SD after neoadjuvant therapy will undergo intermediate tumor cytoreductive surgery, followed by 6 cycles of adjuvant chemotherapy and 1 year of maintenance therapy with the etoricoxib-drug combination antibody regimen. The primary endpoint is R0 resection rate, aiming to provide valuable insights into neoadjuvant treatment strategies for advanced ovarian cancer patients.

This description comes directly from the study's public registry record.

Talk to the study team

Bai-Rong Xia, MD  ·  18604516165  ·  xiabairong9999@126.com

Yao Chen  ·  cyao49446@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Anhui Cancer HospitalHefei, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07667751