drugset / Trial / NCT03746223

Intravitreal Methotrexate and R2(Rituximab & Lenalidomide) Regimen in Newly-diagnosed Primary Vitreoretinal Lymphoma

NCT03746223 ↗

Phase 2 Unknown 42 enrolled Peking Union Medical College Hospital
NaSingle-groupOpen-labelTreatment

Summary

This is a prospective single arm phase II study, and the purpose of this study is to evaluate the efficiency of R2 regimen (rituximab \& lenalidomide) combined with intravitreal methotrexate and followed by lenalidomide maintenance in newly-diagnosed primary intraocular lymphoma. Progression free survival (PFS) of the cohort is the primary endpoint.

Timeline

Start
2018-11-15
Primary completion
2020-11-15
Completion
2025-10-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 25 mg Oral
Subject Methotrexate Small molecule 400 ug Intravitreal
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications