drugset / Trial / NCT04516655

A Phase II Trail of Chidamide ,Rituximab and Methotrexate in Lymphoma Patients

NCT04516655 ↗

Phase 2 Unknown 51 enrolled Fudan University
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy, safety and patient reported outcomes of chidamide 20 mg biw PO day1-14 and rituximab 375 mg/m2 IV given on day 1 and methotrexate 3.5g/m2 IV given on day 2 of every 21-day cycle for 6 cycles in untreated patients with primary central nervous system lymphoma. The primary study endpoint will be complete response (CR) rate as assessed by the investigator. The hypothesis is previously untreated patients with primary central nervous system lymphoma could achieve a CR rate of 80% with C-R-HDMTX.

Timeline

Start
2020-09-01
Primary completion
2021-09-01
Completion
2023-08-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Methotrexate Small molecule 3.5 g Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Subject Tucidinostat Small molecule 20 mg —