Condition: Cervical Cancer · Sponsor: Fujian Cancer Hospital
Cadonilimab, a PD-1/CTLA-4 bi-specific antibody, is being developed by Akeso, Inc. for the treatment of a range of solid tumors, including cervical cancer, lung cancer, gastric/gastroesophageal junction cancer, liver cancer and nasopharyngeal cancer. Cadonilimab was approved in China in June 2022 for use in patients with relapsed or metastatic cervical cancer who have progressed on or after platinum-based chemotherapy. The clinicopathological data of patients with persistent, recurrent or metastatic cervical cancer treated with Cadonilimab were collected, and medical images (magnetic resonance, CT, etc.) before and after treatment were followed up, and the efficacy was evaluated according to RECIST standards. The incidence and severity of adverse events and clinically significant abnormal laboratory test results were collected to evaluate the safety of the drug. Survival benefit analysis is conducted based on the patient's survival time and medical expenses.
This description comes directly from the study's public registry record.
Yang Sun, Master · 15959028989 · doctorsunyang@sina.com
Jian Chen · 15806030009 · marsz3@126.com
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| No. 420 Fuma Road, Jin'an District, Fuzhou City, Fujian Province | Fuzhou, Fujian, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06140589