H01 in Adults With Interstitial Lung Disease (The SOLIS Study)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-100
SponsorNational Institute of Environmental Health Sciences (NIEHS)

About this trial

Background:

Interstitial lung disease affects the tissues that aid the transfer of oxygen and carbon dioxide between the air and the bloodstream. The disease can cause fibrosis, a thickening and scarring of lung tissue. Fibrosis often continues getting worse, and most people with this disease die in 3 to 5 years.

Objective:

To test a study drug (hymecromone) in people with interstitial lung disease or lung fibrosis.

Eligibility:

People aged 18 years and older with interstitial lung disease or lung fibrosis.

Design:

Participants will have at least 7 clinic visits over 5 months.

Participants will have screening and baseline visits. They will have blood tests and tests of their heart function. They will give a sputum sample. Other tests will include:

Spirometry: Participants will breathe in and out through a mouthpiece to measure how much air they can hold in their lungs and how hard they can breathe.

Diffusion capacity of lungs for carbon monoxide: Participants will breathe in a gas that contains a small amount of carbon monoxide. Then they will breathe through a mouthpiece. This test measures how well oxygen moves from the air into the blood.

Resting energy expenditure. Participants will lie still for 30 minutes with a clear dome over their head. This test measures the calories their body burns at rest.

6-minute walk test. Participants will walk at their normal pace for 6 minutes. Their vital signs and blood oxygen levels will be checked.

Hymecromone is a tablet taken by mouth. Participants will take 2 tablets every morning and 2 tablets every night for 12 weeks. Tests will be repeated at study visits.

Eligibility criteria

Qualifiers

Ability of subject to understand, and the willingness to sign a written informed consent document and comply with requirements of the study

Stated willingness to comply with all study procedures and availability for the duration of the study

Male or Female participants ages >18 years

MD diagnosis of Idiopathic Pulmonary Fibrosis or other progressive ILD as defined previously

Disqualifiers

Active on lung transplantation list

On supplemental oxygen at rest

Evidence of an acute respiratory infection or exacerbation of pulmonary fibrosis

Known diagnosis of celiac disease or wheat or gluten allergies

Trial design

Treatments tested in this trial

  • hymecromone

Treatment groups

37 Participants
are divided into 1 treatment group