Clin2
NCT07604766Possibly a fitRecruiting

Rina-S for platinum-resistant ovarian cancer in China

Platinum-resistant Ovarian Cancer

Treatments studied

Part of Cancer, Hormones & metabolism, Women’s health & pregnancy clinical trials.

This study tests a new cancer drug called Rina-S (an antibody-drug conjugate, which is a targeted therapy that delivers medicine directly to cancer cells) compared to standard treatment options for ovarian cancer that has returned or worsened after platinum chemotherapy. The trial is specifically for patients in China whose cancer is resistant to platinum drugs.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
82 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Diagnosed with high-grade serous or endometrioid ovarian cancer, primary peritoneal cancer, or fallopian tube cancer confirmed by tissue biopsy
  • Previously received 1 to 4 lines of cancer treatment, with cancer that has grown back after the most recent treatment
  • Must have received platinum chemotherapy in the past; if bevacizumab was standard in your region, you should have received it (unless you couldn't tolerate it); if you have a BRCA gene mutation and responded well to platinum therapy, you should have received PARP inhibitor maintenance treatment
  • Have 'platinum-resistant' disease, meaning cancer progressed 92–183 days after your first platinum therapy, or within 183 days if you've had multiple lines of platinum therapy
  • No eye problems that would make you ineligible for mirvetuximab soravtansine (such as corneal transplant, uncontrolled glaucoma, wet macular degeneration, or vision in only one eye)
  • No severe fluid buildup in the abdomen or around the lungs that requires draining more than every 4 weeks, and no bowel obstruction in the past 3 months

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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