Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING

Safety and Durability of Sirolimus for Treatment of LAM

NCT02432560 · View on ClinicalTrials.gov ↗

Study 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.

Conditions Studied

Interventions

  • DRUG Sirolimus
  • DRUG Everolimus

Study Locations (20)

Ohio

  • University of Cincinnati — Cincinnati
  • Cleveland Clinic — Cleveland

Texas

  • University of Texas Southwestern Medical Center — Dallas
  • University of Texas Health Center — Houston

California

  • Stanford University Medical Center — Stanford

Colorado

  • National Jewish Health — Denver

Florida

  • Mayo Clinic Jacksonville — Jacksonville

Georgia

  • Emory University School of Medicine — Atlanta

Illinois

  • Loyola University Medical Center, Chicago — Maywood

Massachusetts

  • Brigham and Women's Hospital — Boston

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2015-03
Est. Completion 2025-07-31

Sponsor

University of Cincinnati

179 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02432560

The ClinicalTrials.gov registry entry for NCT02432560 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Cincinnati, which has 179 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Lymphangioleiomyomatosis appearing as the primary indexed condition, and to 2 interventions — of which Sirolimus is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02432560 reports 20 study locations spanning 18 distinct geographic areas — top geographies include Ohio, Texas, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02432560 about?

NCT02432560 is a clinical study titled "Safety and Durability of Sirolimus for Treatment of LAM". 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 wi...

What is the current status of trial NCT02432560?

This trial is currently recruiting. The enrollment target is 600 participants. The study started on 2015-03. Estimated completion is 2025-07-31.

What conditions does trial NCT02432560 study?

This clinical trial studies the following conditions: Lymphangioleiomyomatosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02432560?

The interventions under investigation include: Sirolimus (DRUG), Everolimus (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02432560?

This trial is sponsored by University of Cincinnati, which has 179 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02432560 being conducted?

This trial has 20 study locations across California, Colorado, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial