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Clinical Trial Summary

This is a prospective, multicenter, open label Phase II Clinical Trial. 30 advanced poorly differentiated thyroid carcinoma patients who were histopathologically confirmed inoperable were enrolled in this study.


Clinical Trial Description

Subjects will receive the treatment regimen as follow:

intravenous infusion of liposomal doxorubicin 35 mg/m2, d1; cisplatin 75 mg/m2, drip, total dose should be carried out on d1-3; once every 21days, for 6 cycles. Stop the treatment if the patients have progressed or intolerated to the toxicity. The primary endpoint is disease control rate(DCR), the secondary endpoint is overall survival (OS), progression-free survival (PFS), safety and quality of life assessment(QoL). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03387943
Study type Interventional
Source CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Contact jiandong nie, doctor
Phone 0311-66575708
Email niejd@mail.ecspc.com
Status Recruiting
Phase Phase 2
Start date March 6, 2017
Completion date December 31, 2019