A Single Dose, Dose Escalation Clinical Trial on the Safety, Tolerability and Efficacy of Lyophilized Powder for Inhalation of Recombinant Human Keratinocyte Growth Factor-2 (Rh-KGF-2) in The Treatment of Patients With Acute Respiratory Distress Syndrome

Prior treatment

• History of severe allergic reaction, or known allergy or hypersensitivity to any component of the investigational product.
• Participation in any drug clinical trial within 3 months prior to enrollment.

Other illness

• Expected survival \< 3 months due to causes other than respiratory failure.
• Any other condition that, in the opinion of the investigator, makes the subject unsuitable for participation in this study.

Lab values

• Cerebrovascular or cardiovascular events within 3 months prior to study drug administration, including unstable angina, congestive heart failure, myocardial infarction within the past 12 months, hemodynamic instability, known left ventricular ejection fraction (LVEF) \< 40%, or clinically significant arrhythmia or conduction abnormality.
• Inability to tolerate single-use bronchoscopic imaging catheter examination, including but not limited to the following: active massive hemoptysis; severe hypertension and arrhythmia; myocardial infarction or unstable angina within 4-6 weeks prior to screening; severe cardiac dysfunction; uncorrectable bleeding tendency (platelet count \< 60 × 10⁹/L), such as severe coagulation disorders, uremia, or severe pulmonary hypertension; severe superior vena cava syndrome; suspected aortic aneurysm; multiple pulmonary bullae.

Other

• Use of inhaled pulmonary vasodilators (e.g., nitric oxide or prostaglandins).
• Current receipt or planned receipt of extracorporeal membrane oxygenation (ECMO) during the study period.
• Breastfeeding or pregnant women.

• Aged ≥18 years and \<80 years, male or female.
• Definite diagnosis of acute respiratory distress syndrome (ARDS) according to the Berlin Definition.
• Patients with PaO₂/FiO₂ \< 200 mmHg and receiving invasive mechanical ventilation via endotracheal intubation.
• Diagnosis of ARDS confirmed no more than 72 hours prior to enrollment.
• No plan for parenthood within 1 year and agree to take effective contraceptive measures during the study period. Female participants of childbearing potential must have a negative serum pregnancy test.
• The subject fully understands the purpose of the study, as well as the nature, methods, and potential reactions of the investigational drug. The subject voluntarily signs the informed consent form to participate in the study and agrees to comply with the requirements of the study protocol. If the subject is unable to provide consent or has limited capacity to consent, consent must be obtained from the subject's legal guardian.
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