drugset / Trial / NCT06293716

CVL237 Tablets for APDS/PASLI

NCT06293716 ↗

Phase 2/3 Unknown 35 enrolled Convalife (Shanghai) Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study was designed to evaluate the efficacy and safety of CVL237 tablets in patients with APDS/PASLI (activated phosphoinositol 3-kinase δ syndrome /p110 delta-activated mutation leading to senescent T cells, lymphadenopathy, and immune deficiency).

Timeline

Start
2024-03-30
Primary completion
2025-12-29
Completion
2026-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject CVL237 Unknown 100 mg Oral
Subject CVL237 Unknown 200 mg Oral