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Intrathecal Dual Checkpoint Inhibitor (PD-1 and CTLA-4) in Combination With Pemetrexed for Leptomeningeal Metastasis
RECRUITINGPhase 1/2Sponsored by Guangzhou Medical University
Actively Recruiting
PhasePhase 1/2
SponsorGuangzhou Medical University
Started2025-03-17
Est. completion2026-06-01
Eligibility
Age21 Years – 75 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06809530
Summary
This phase I/II study is to evaluate the recommended dose, safety, feasibility, and therapeutic response of intrathecal dual checkpoint inhibitor (targeting PD-1 and CTLA-4 with QL1706) in combination with pemetrexed in patients with leptomeningeal metastasis.
Eligibility
Age: 21 Years – 75 YearsHealthy volunteers accepted
Inclusion Criteria: 1. Histologically or cytologically confirmed diagnosis of solid tumors; Cerebrospinal fluid cytopathology is positive. 2. Male or female aged between 21 and 75 years; Normal liver and kidney function; WBC≥4000/mm3, Plt≥100000/mm3. 3. No history of severe nervous system disease; No severe dyscrasia. Exclusion Criteria: 1. Any evidence of nervous system failure, including severe encephalopathy, grade 3 or 4 leukoencephalopathy on imaging, and Glasgow Coma Score less than 11. 2. Any evidence of extensive and lethal progressive systemic diseases without effective treatment. 3. A history of HIV or AIDS, acute or chronic hepatitis B or C infection, previous anti-PD1 therapy-induced pneumonitis, or have ongoing \>Grade 2 adverse events of such therapy; or ongoing autoimmune disease that required systemic treatment in the past 2 years. 4. Patients with poor compliance or other reasons that were unsuitable for this study.
Conditions6
CTLA4CancerLeptomeningeal MetastasisPD-1 InhibitorPemetrexedSolid Tumors
Interventions2
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Actively Recruiting
PhasePhase 1/2
SponsorGuangzhou Medical University
Started2025-03-17
Est. completion2026-06-01
Eligibility
Age21 Years – 75 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06809530