drugset / Trial / NCT06504420

The Safety and Efficiency of Sirolimus in Primary Antiphospholipid Syndrome: a Randomized Control Study

NCT06504420 ↗

Phase 2 Not yet recruiting 70 enrolled Peking University People's Hospital
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is an Investigator initiated, randomized, multicenter, double-blind, placebo-control study. The aim of this study is to evaluate the safety and efficiency of Sirolimus for primaty antiphospholipid syndrome patients at week 24 and week 48.

Timeline

Start
2024-10-15
Primary completion
2026-12-30
Completion
2027-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirolimus Small molecule 1.5 mg Oral