Clin2
NCT01799538Possibly a fitRecruiting

Inhaled albuterol for lung disease LAM

Lymphangioleiomyomatosis

Part of Blood & lymphatic, Cancer, Immune system & allergy clinical trials.

This Phase 1/2 study tests whether breathing in albuterol can improve symptoms or lung function in people with lymphangioleiomyomatosis (LAM). It’s mainly about safety and early signs of benefit by targeting airflow problems.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
100 people
Ages
18 years to 100 years
Study type
Interventional

Who can take part

  • You have a confirmed diagnosis of LAM (or LAM linked to tuberous sclerosis), based on medical testing or evidence in lungs/other organs
  • You are 18 years or older
  • Your breathing test shows airflow blockage (low FEV1 and a low FEV1/VC ratio)
  • You are not allergic to albuterol (or its ingredients)
  • You do not have moderate or large fluid around the lung (pleural effusion)
  • You can stop certain breathing medicines for 24 hours before the study (and, if relevant, stop some other specific drugs for at least 7 days)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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