Condition: PCNSL · Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University
This is a prospective, multicenter, single-arm, open Phase Ib/II clinical study to explore the safety and efficacy of pomadomide in combination with rituximab and methotrexate (RPM) in newly diagnosed primary central nervous system lymphoma (PCNSL) subjects. The Phase I study is a dose escalation study, in which rituximab and methotrexate are fixed doses, and pomadomide is set into 3 dose groups: 3mg/d, 4mg/d and 5mg/d. In strict accordance with the "3+3" dose escalation principle, 3-6 subjects are to be recruited in each dose group, and each subject is to be observed for 1 cycle after treatment to determine MTD. Phase II study: RP2D is planned to be determined based on the Phase Ib study, with an additional 25 active participants enrolled to further evaluate efficacy and safety. Subjects with initial treatment of PCNSL who met the inclusion/exclusion criteria were screened, and after signing the informed consent letter, they received 4 courses of PRM regimen. The patients achieving CR or PR were consolidated by autologous transplantation consolidation regimen or the original regimen for 2 courses, and then were given pomadomide maintenance therapy for 12 cycles. Follow-ups should be taken up to the first 3 years.
This description comes directly from the study's public registry record.
Xianggui Yuan, Doctor · +8613989883884 · yuanxg@zju.edu.cn
Wenbin Qian · +8613605801032 · qianwb@zju.edu.cn
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| 2nd Affiliated Hospital, School of Medicine, Zhejiang University | Hanzhou, Zhejiang, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06554561