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Pulmonary Vascular
Pulmonary Vascular Disease Inhalation / Device Combination
Sustained Release


Pulmonary Arterial Hypertension (PAH)


PAH refers to the condition where the pulmonary arteries in the lungs narrow, thicken, or stiffen, leading to high pressure in the pulmonary blood vessels. This requires the right ventricle of the heart to contract with increased force in order to pump blood from the right ventricle through the narrowed arteries to the lungs. Over time, this condition leads to right-sided heart enlargement and eventually right ventricular failure, which can be fatal. The primary cause of idiopathic pulmonary arterial hypertension is usually of unknown cause and it is a rare disease that progresses rapidly. According to data from the US National Institutes of Health (NIH), untreated patients with pulmonary arterial hypertension have an average survival rate of approximately 2.8 years.


Since pulmonary arterial hypertension cannot be cured, lifelong medication is necessary to slow down the progression of the disease. Currently, the main treatment approach involves using targeted drugs that act on the prostacyclin pathway, along with other supportive medications, to control symptoms. In later stages, medications with different mechanisms or lung transplantation may be considered. However, the side effects of existing medications include limitations on the dosage and inability to adjust to a higher dosage based on the individual’s condition. Furthermore, high frequency of use also affects patients’ daily lives.


The L606 formulation is designed to encapsulate prostacyclin drugs in liposomes, providing localized and sustained release characteristics. It also reduces the frequency of daily dosing and allows for dosage adjustments based on the disease progression, significantly improving patients' quality of life.


Based on market strategy planning, the treatment of pulmonary arterial hypertension with L606 will prioritize the North American market.



Interstitial Lung Disease-Associated Pulmonary Hypertension (PH-ILD)


Interstitial lung disease-associated pulmonary hypertension refers to pulmonary hypertension caused by lung diseases or chronic hypoxia. Interstitial lung disease leads to the continuous formation of scar tissue in the alveoli, resulting in lung stiffness or fibrosis and triggering pulmonary hypertension. This is an irreversible disease. As the condition worsens, patients experience difficulty breathing, eventually leading to right ventricular failure and respiratory failure.


The current treatment approach focuses on providing symptom relief, improving quality of life, and slowing disease progression. The latest targeted medications are inhaled prostacyclin analogs, which require dosing regimen of four times a day. Inhaling high concentration of quick-releasing medication can cause discomfort in the respiratory tract, and drug administration during sleep can be challenging, hence affecting medication efficacy.


The L606 formulation is designed to encapsulate prostacyclin drugs in liposomes, providing a stable drug release rate that reduces side effects and the frequency of administration. It also effectively reduces respiratory tract irritation during inhalation.


The priority market for the treatment of interstitial lung disease-associated pulmonary hypertension with L606 is North America, followed by expansion into Europe and Asia.