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Phase II clinical study of RMPD for initial treatment of PCNSL

A prospective, single-arm, multicenter, Phase II clinical study of pomadomide combined with rituximab, methotrexate, dexamethasone regimen for the treatment of primary central nervous system lymphoma

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093682
Enrollment
Unknown
Registered
2024-12-10
Start date
2024-12-10
Completion date
Unknown
Last updated
2024-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary central nervous system lymphoma

Interventions

experimental group:Pomadomide combined with rituximab, methotrexate, dexamethasone regimen

Sponsors

Chongqing University Affiliated Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18-70 years old, male or female, expected survival time: 3 months or more 2. Patients with primary central nervous system lymphoma diagnosed as CD20 positive by pathology without prior treatment 3. Signed an informed consent form before performing any specific operation 4. The patient has sufficient organ function, including: blood routine: ANC>=1 × 10 ^ 9/L, Hb>=80g/L, PLT>=75 × 109/L; Liver function results (total bilirubin40ml/min 5. At least one measurable lesion; 6. Researchers determine that patients with an expected life expectancy of at least 3 months

Exclusion criteria

Exclusion criteria: 1. If there is an allergic reaction to pomalidomide capsules or any excipients 2. Merge other uncontrolled malignant tumors 3. Severe heart failure (NYHA grade 3-4) 4. Accompanied by uncontrolled cardiovascular and cerebrovascular diseases 5. Adopt other anti-tumor treatments outside of this research protocol 6. Pregnant or lactating women 7. There are clinical situations where other researchers consider it inappropriate to participate in this study

Design outcomes

Primary

MeasureTime frame
Complete response rate in the induced remission phase;Total response rate during induced remission phase;

Countries

China

Contacts

Public ContactYao Liu

chongqing university cancer hospital

648283926@qq.com+86 23 65079270

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026