Nebulized Human Amniotic Fluid in Patients With Interstitial Lung Disease (HAF ILD)

Maule Stem Cell Research Institute, Inc.

Status and phase: Enrolling; Phase 1

Conditions: Lung Diseases, Interstitial

Treatments: Biological: Matrix

Study type: Interventional

Funder types: Other

Identifiers

NCT07372989

2025-MSCRI-001

Details and patient eligibility

About

This is a Phase I, pilot clinical trial designed to evaluate the safety and exploratory efficacy of nebulized diluted amniotic fluid, Matrix (HAF-Matrix) in adults with interstitial lung disease (ILD). ILDs are progressive fibrotic disorders characterized by aberrant wound-healing responses, chronic inflammation, and dysregulated fibroblast activation, ultimately leading to impaired gas exchange and respiratory failure. Current treatments, such as antifibrotic agents (pirfenidone and nintedanib), slow disease progression but do not reverse existing fibrosis or restore lung function. This pilot study will generate critical safety and preliminary efficacy data to inform future larger-scale trials and optimize dosing strategies for nebulized HAF-based therapeutics in ILD.

Full description

This pilot study will generate critical safety and preliminary efficacy data to inform future larger-scale trials and optimize dosing strategies for nebulized EV-based therapeutics in ILD.

Two-part seamless design:

Dose Escalation Approach with a 3+3 (Cohort A = 3, Cohort B = 3) Total of 6 Participants Design with Staggered Dosing:

1. Cohort Enrollment and Initial Dosing

• At each prespecified dose level, three (3) subjects will be enrolled and dosed.

The first subject in each cohort will be dosed initially, followed by the second and third subjects according to planned staggered intervals, ensuring careful monitoring of early safety signals.

Post 3x3 run-in phase, The Phase 1(open label) will begin:

• 2 Cohorts of 22 participants per cohort:
• Doses 1.0 ml and 1.5 ml of Matrix via mesh nebulizer:

Cohort A, n=22: 1×10^9 particles Cohort B, n=22: 1×10^12 particles (Dose range anchored to inhaled-EV clinical experience.)

Enrollment: 50 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

In order to participate in this study, a patient MUST:

• Provide written informed consent.
• Subjects age > 40 and < 90 years at the time of signing the Informed Consent Form.
• Have a clinical diagnosis of ILD prior to screening in accordance with the guidelines of the American Thoracic Society/European Respiratory Society.
• FVC ≥ 45% predicted and DLCO ≥30% (corrected for hemoglobin but not alveolar volume).
• Resting SpO₂ ≥ 92% on ≤ 3 L/min O₂.
• RVSP < 50 mmHg, as documented by Doppler echo or right heart catheterization.
• Female subjects must be surgically sterile or post-menopausal (>1 year).

Exclusion criteria

In order to participate in this study, a patient MUST NOT:

• CT and/or surgical lung biopsy results inconsistent with the diagnosis of IPF.
• Inability to perform any of the assessments required for endpoint analysis (report safety or tolerability concerns, perform PFTs or CT, undergo blood draws, read and respond to questionnaires.)
• Currently receiving (or received within four weeks of screening) any medication, treatment, or experimental agents for the treatment of ILD, except for patients receiving non-drug therapies will include oxygen saturation therapy (oxygen supplementation) and pulmonary rehabilitation.
• Active listing (or expected future listing) for transplant of any organ.
• Clinically important abnormal screening laboratory values, including but not limited to: hemoglobin <8 g/dl, white blood cell count <3000/mm3, platelets <80,000/mm3, INR > 1.5, aspartate transaminase, alanine transaminase, or alkaline phosphatase > 2 times upper limit of normal, total bilirubin > 1.5 mg/dl.
• Serious comorbid illness that, in the opinion of the investigator, may compromise the safety or compliance of the patient or preclude successful completion of the study. Including, but not limited to: HIV, advanced liver or renal failure, class III/IV congestive heart failure, myocardial infarction, unstable angina, or cardiac revascularization within the last six months, or severe obstructive ventilatory defect.
• Any other condition that, in the opinion of the investigator, may compromise the safety or compliance of the patient or preclude successful completion of the study.
• Be an organ transplant recipient.
• Have a clinical history of malignancy within 2.5 years (i.e., patients with prior malignancy must be disease free for 2.5 years), except curatively treated basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma.
• Have a non-pulmonary condition that limits lifespan to < 1 year.
• Have a history of drug or alcohol abuse within the past 24 months.
• Be serum positive for HIV, hepatitis BsAg or Viremic hepatitis C.
• Be currently participating (or participated within the previous 30 days) in an investigational therapeutic or device trial.
• Be a female who is pregnant, nursing, or of childbearing potential while not practicing effective contraceptive methods. Female patients must undergo a blood or urine pregnancy test at screening and within 36 hours prior to injection.
• Female subjects must have an FSH < 25.8 IU/L
• Subject with hypersensitivity to dimethyl sulfoxide (DMSO)
• Saturated oxygen (SpO2 of < 93% (room air [sea level] at rest). SpO2 of < 88% (room air [>5,000 feet above sea level (1524 meters) at rest).

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

Cohort A

Experimental group

Description:

1.0 mL of Matrix (Exosomes)

Treatment:

Biological: Matrix

Cohort B

Experimental group

Description:

1.5 mL of Matrix (Exosomes)

Treatment:

Biological: Matrix