Iparomlimab (QL1604) in patients with microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) unresectable or metastatic solid tumors: a pivotal, single-arm, multicenter, phase II trial

Though several anti-PD-1/PD-L1 antibodies approved for monotherapy in microsatellite instability-high or mismatch repair-deficient unresectable/metastatic solid tumors, novel immunotherapy with better anti-tumor activity is needed in clinic. In this single-arm, multicenter, pivotal, phase II study,...

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Veröffentlicht in:Journal of hematology and oncology 2024-11, Vol.17 (1), p.109-5, Article 109
Hauptverfasser: Bi, Feng, Dong, Jian, Jin, Chuan, Niu, Zuoxing, Yang, Wenhui, He, Yifu, Yu, Dajun, Sun, Meili, Wang, Teng, Yin, Xianli, Zhang, Ruixing, Chen, Kehe, Wang, Keming, Wang, Zhiwu, Li, Wei, Zhang, Zhongtao, Zhang, Hangyu, Guo, Qunyi, Wang, Xin, Han, Lei, Zhang, Xizhi, Shen, Wei, Zhang, Liangming, Ying, Jieer, Wu, Miao, Hu, Weiguo, Li, Zeng, Li, Xiaofen, Feng, Wenlei, Zhang, Baihui, Li, Lingyan, Kang, Xiaoyan, Guo, Weijian
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Sprache:eng
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Zusammenfassung:Though several anti-PD-1/PD-L1 antibodies approved for monotherapy in microsatellite instability-high or mismatch repair-deficient unresectable/metastatic solid tumors, novel immunotherapy with better anti-tumor activity is needed in clinic. In this single-arm, multicenter, pivotal, phase II study, patients received iparomlimab (a novel humanized anti-PD-1 mAb, 200 mg or 3 mg/kg for patients with body weight 
ISSN:1756-8722
1756-8722
DOI:10.1186/s13045-024-01627-5