drugset / Trial / NCT03987152

Treatment of Congenital Vascular Malformations Using Sirolimus: Improving Quality of Life

NCT03987152

Phase 3 Unknown 75 enrolled Radboud University Medical Center
NaSequentialOpen-labelTreatment

Summary

Congenital vascular anomalies are uncommon and belong to the group of rare diseases.These vascular malformations can cause serious complications including obstruction of vital organs and their function, recurrent infection and significantly reduced quality of life of persons affected.Treatment options range from conservative to surgical extirpation or intralesional embolisation/sclerosis. Unfortunately, this is often not enough. Many patients still have complaints like severe pain and invalidation due to the lymphatic or venous malformation making a normal functional life impossible. Recent case reports mention the positive effects of refractory patients with Sirolimus. Sirolimus, also known as rapamycin, is currently the only FDA-approved mammalian target of rapamycin (mTOR) inhibitor.

Timeline

Start
2017-09-18
Primary completion
2021-09-18
Completion
2023-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirolimus Small molecule

Indications