Safety and Durability of Sirolimus for Treatment of LAM

Recruiting now

Conditions studied: Lymphangioleiomyomatosis

In brief

The MIDAS study aims to follow male and female LAM patients who are currently taking, have previously failed or been intolerant of, or may (at some time in the future) take mTOR inhibitors (sirolimus or everolimus) as part of their clinical care. Adult female TSC patients may also enroll, with or without lung cysts.

Key facts

Study ID
NCT02432560
Run by
University of Cincinnati
People needed
600
Starts
2015-03-01
Expected to finish
2025-07-31
Last updated by the study team
2024-12-24

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.