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180
3 进行中
药物批准
16
批准总数
监管机构
2
监管机构数
成立时间
1984
进行中(未招募)
1.1%
已完成
151
83.9%
尚未招募
1
0.6%
招募中
5
2.8%
终止
18
10.0%
撤回
3
1.7%
NMPA
National Medical Products Administration
FDA
Food and Drug Administration
14
- The checkpoint inhibitor refractory cancer market is expected to grow significantly by 2036, driven by rising resistance to immune checkpoint inhibitors and demand for next-generation therapies. - Approximately 40–60% of patients with melanoma, NSCLC, renal cell carcinoma, urothelial carcinoma, and head and neck cancers experience primary resistance to PD-1/PD-L1 inhibitor therapy. - Promising investigational therapies include Sitravatinib + Nivolumab, TAVO + Pembrolizumab, Botensilimab + Balstilimab, and ICT01, which aim to overcome resistance and restore antitumor immunity. - The United States accounted for the largest checkpoint inhibitor refractory cancer treatment market size in the 7MM in 2025.