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Safety and Durability of Sirolimus for Treatment of LAM

RECRUITINGSponsored by University of Cincinnati
Actively Recruiting
SponsorUniversity of Cincinnati
Started2015-03
Est. completion2025-07-31
Eligibility
Age18 Years+
SexFEMALE
Healthy vol.Accepted
Locations20 sites

Summary

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.

Eligibility

Age: 18 Years+Sex: FEMALEHealthy volunteers accepted
Inclusion Criteria:

* Female or male, age 18 or over
* Diagnosis of LAM based on ATS/JRS criteria
* Signed and dated informed consent
* On chronic therapy, newly treated or may be considered for therapy with mTOR inhibitors or previously intolerant of or having failed mTOR inhibitor therapy

Exclusion Criteria:

* Inability to attend at least one RLD Clinic visit per year
* Inability to give informed consent
* Inability or unwillingness to perform pulmonary function testing

Conditions3

CancerLung CancerLymphangioleiomyomatosis

Locations20 sites

Stanford University Medical Center
Stanford, California, 94305
Stephen Ruoss, MD650-723-6381ruoss@stanford.edu
National Jewish Health
Denver, Colorado, 80206
Gregory Downey, MD303-398-1436gregory.downey@gmail.com
Mayo Clinic Jacksonville
Jacksonville, Florida, 32224
Charles Burger, MD904-953-2381charles.burger@mayo.edu
Emory University School of Medicine
Atlanta, Georgia, 33136
Sirhari Veeraraghavan, MDveeraraghavan@emory.edu
Loyola University Medical Center, Chicago
Maywood, Illinois, 60153

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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