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Clinical Trial Summary

This is a single-center, open-label, cohort clinical study to investigate the efficacy and safety of surufatinib with or without immunotherapy in patients with advanced colorectal cancer who failed front-line anti-angiogenic TKI therapy. Patients have to received at least a second-line standard therapy or cannot tolerate other treatments, and have previously failed anti-angiogenic TKIs therapy(including but not limited to: fruquintinib/regorafenib/anlotinib) / apatinib, and are resistant to treatment, disease progression, intolerable toxicity or no continued benefit as assessed by investigator after therapy). Patients who met the eligibility criteria are randomized 1:2 into two cohorts (cohort 1: surufatinib, cohort 2: surufatinib plus immunotherapy) to receive treatment until disease progression, death, unacceptable toxicity, withdrawal of consent by the patient, or decision by the treating physician that discontinuation would be in the patient's best interest. The primary study endpoint was PFS(progression free survival).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05372198
Study type Interventional
Source Hubei Cancer Hospital
Contact Xu Huiting, M.D.
Phone +86-15307176219
Email 2891533@qq.com
Status Recruiting
Phase Phase 2
Start date March 30, 2022
Completion date December 2024

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