RecruitingNCT06917196

PROOF OF CONCEPT STUDY ON THE EFFICACY OF INHALATORY TARGETED IMATINIB NANOFORMULATIONS IN PULMONARY HYPERTENSION AND POST-INFLAMMATORY FIBROSIS.


Sponsor

Fondazione IRCCS Policlinico San Matteo di Pavia

Enrollment

16 participants

Start Date

Dec 4, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

The PROMPTLY study is a proof-of-concept research project evaluating the efficacy of XHALIP, an innovative inhalable formulation of Imatinib, in treating pulmonary arterial hypertension (PAH) and post-inflammatory fibrosing lung diseases (LFD). Main Objective To demonstrate the ability of XHALIP to improve the prognosis of PAH and LFD by reducing pulmonary fibrosis and vascular remodeling. Key Research Questions Is XHALIP effectively absorbed by pathological lung cells? Does it have a beneficial biological effect on cell proliferation and extracellular matrix deposition? Study Plan Preclinical phase: In vitro tests on cells obtained from patients with PAH and LFD. Absorption and distribution analysis: In vitro lung tissue models to assess drug penetration and effectiveness. Biological activity assessment: Evaluating XHALIP's ability to inhibit epithelial-mesenchymal transition and cell proliferation. Participants Patients aged ≥ 18 years diagnosed with PAH or LFD, either candidates for or recipients of lung transplantation. Biological samples (bronchoalveolar lavage and explanted lung tissues). Methodology Confocal microscopy and flow cytometry to analyze absorption. RT-PCR and Western Blot to assess biological efficacy. Alveolo-capillary models to test drug release and distribution. The study aims to translate preclinical findings into a potential future clinical trial for the development of XHALIP as a novel inhalation-based therapeutic strategy for rare lung diseases.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This proof-of-concept study is testing an inhaled form of imatinib (a drug normally taken as a pill) delivered as tiny nanoparticles directly into the lungs. Researchers want to see if this targeted delivery approach can treat pulmonary arterial hypertension (high blood pressure in the lungs) and lung fibrosis (scarring). **You may be eligible if...** - You are 18 or older - You have been diagnosed with a fibrosing lung disease, obliterative bronchiolitis (airway scarring), or pulmonary arterial hypertension (PAH) - You are a candidate for or have already undergone a lung transplant - You have provided informed consent **You may NOT be eligible if...** - You have suspected or confirmed lung cancer Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Fondazione IRCCS Policlinico San Matteo

Pavia, Pavia, Italy

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NCT06917196


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