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Clinical Trial Summary

The purpose is to evaluate the effectiveness and safety of Surufatinib in patients with osteosarcoma and soft tissue sarcoma after Standard chemotherapy therapy.


Clinical Trial Description

The study population is patients with advanced osteosarcoma and soft tissue sarcoma who have failed in standard chemotherapy treatment. Surufatinib 300 mg once a day (QD) will be orally administrated on a 21-day cycle. Investigators will evaluate the clinical tumor response to Surufatinib, and if investigators determine that the patient can benefit from the continuation of treatment, the patient will continue the Surufatinib treatment. The duration of study will be 2 years. At the time of study completion, if investigators believe patients can continue to benefit from the investigational product, patients may be provided with Surufatinib with the agreement of the sponsor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05106777
Study type Interventional
Source Sun Yat-sen University
Contact Xing Zhang, professor
Phone 020-87343383
Email zhangxing@sysucc.org.cn
Status Recruiting
Phase Phase 2
Start date December 10, 2021
Completion date December 10, 2023

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