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

National Institutes of Health (NIH)

Status and phase

Enrolling

Phase 2

Conditions

Lung Diseases, Interstitial

Idiopathic Pulmonary Fibrosis

Interstitial Lung Disease

Treatments

Drug: hymecromone

Study type

Interventional

Funder types

NIH

Identifiers

NCT06325696

001577-E

10001577

Details and patient eligibility

About

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.

Full description

Study Description:

Phase 2a, open-label, study to evaluate the safety, tolerability, and efficacy of H01 in adults with progressive interstitial lung disease. Up to 37 participants will be enrolled.

Objectives:

Primary Objective: Evaluate the efficacy of H01 in reducing hyaluronan levels in participants with progressive interstitial lung disease.

Secondary Objectives:

Evaluate the safety and tolerability of oral H01 in participants with progressive interstitial lung disease.
Evaluate the change in clinical and functional measures in participants with progressive interstitial lung disease treated with H01.
Evaluate biomarkers of fibrosis in participants with progressive interstitial lung disease treated with H01.
Evaluate pharmacokinetic changes from baseline in participants with progressive interstitial lung disease treated with H01

Endpoints:

Primary Endpoint: Serum HA levels before and after initiation of treatment with H01 over a period of 12 weeks.

Secondary Endpoints:

Safety and tolerability (according to Common Terminology Criteria for Adverse Events)
Change in sputum hyaluronan levels
Change in 6-minute walk test (6MWT)
Change in pulmonary function test (PFT) including: FVC, DLCO
Change in symptom score on Saint George s Respiratory Questionnaire (SGRQ) and King s Brief Interstitial Lung Disease (KBILD) Questionnaire
Change in right ventricular (RV) pressures in echocardiography before treatment and after 12 weeks of H01 treatment
RV Systolic Pressure, Right Atrial Pressure, presence of pericardial effusion, RV size and function via Tricuspid Annular Plane Systolic Excursion /RV Fractional Area Change, Left Ventricular function and Ejection Fraction

Exploratory:

Markers of fibrosis (e.g., monocyte count, monocyte/lymphocyte ratio, cytokine analysis (other, e.g., circulating fibrocytes)
Pharmacokinetic changes from baseline to study visits and study follow-up for H01 and active metabolite (4-MU, and 4-MUG)

Enrollment

37 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

INCLUSION CRITERIA:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

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
DLCO>30% and FVC>45%
Subjects in reproductive age who are heterosexually active must use an acceptable method of contraception: condoms (male or female) with or without a spermicidal agent, diaphragm or cervical cap with spermicide, IUD, or Hormone-based contraceptive
Agreement to adhere to Lifestyle Considerations throughout study duration

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

Active on lung transplantation list
On supplemental oxygen at rest
Evidence of an acute respiratory infection or exacerbation of pulmonary fibrosis at any time during enrollment or study
Known diagnosis of celiac disease or wheat or gluten allergies
Cirrhosis or active viral or non-viral hepatitis: Bilirubin, AST and ALT values higher than twice the upper range of normal, or a Child-Pugh score of 7 or more
Subjects with history of active Inflammatory Bowel Disease, dysphagia, achalasia, or difficulty swallowing capsules, tablets or pills
Subjects with significant renal impairment defined as eGFR lower than 60 ml/min.
Subjects with a baseline corrected Fridericia's QT interval (QTcF) >450ms or baseline ECG abnormalities which, in the opinion of the study physician, are clinically significant and would place the participant at increased risk for adverse effects.
Subjects with ongoing alcohol or illegal drug use disorder
Subjects who are pregnant, lactating or attempting to conceive
- Participants able to become pregnant (have not completed menopause, had a hysterectomy and/or both tubes and/or both ovaries removed) must use effective birth control methods to try and not become pregnant while participant in this study. Methods include (a) partner vasectomy, (b) bilateral tubal ligation, (c) intrauterine devices (IUDs), (d) hormonal implants (such as Implanon), or (e) other hormonal methods (birth control pills, injections, patches, vaginal rings).
- Male participants able to father children with a partner able to become pregnant must agree to use effective birth control (listed above) to participate in this study.
Known allergy to hymecromone or any component thereof
Chronic therapy with medications that are known potent human UDPglucuronosyltransferase inhibitors: canagliflozin, temazepam, tacrolimus.
Physician concern that participant may not adhere to the study protocol
Current participation in another clinical treatment trial for ILD. May participate after 12 weeks from conclusion of another treatment trial.
Changing dose of other ILD medications over the 3 months prior to baseline
Any condition(s) or diagnosis, both physical or psychological, or physical exam finding that place the participant at increased risk for adverse effects, as determined by the study physician.