A Safety/Efficacy Study of Alprostadil Liposomes for Injection to Treat Lower Extremity Arteriosclerosis Obliterans

This is an interventional treatment trial for Arteriosclerosis Obliterans focused on measuring Arteriosclerosis Obliterans, Atherosclerotic Occlusive Disease of the Lower Extremities, Intermittent Claudication Read More

Inclusion Criteria:

• An established clinical history of Atherosclerotic Occlusive Disease of the Lower Extremities in accordance with the definition by Chinese Medical Association(2015).
• Age>40
• Atherosclerotic Occlusive Disease of the Lower Extremities diagnosis
• Arterial ischemia of the lower extremities pulsation has been weakened or disappeared.
• Ankle brachial index(ABI) less than or equal to 0.9
• Diagnosis of artery stenosis or occlusion with imaging tests,including Doppler ultrasonography,CT angiogram(CTA),magnetic resonance angiography (MRA) or digital subtraction angiography(DSA) within 1 month prior to Screening.
• Fontaine stage classification:Stage II
• Distance of asymptomatic disease and claudication between 50m to 800m(The treadmill setting:pace at 3 km/h,incline at 12%).Subjects have intermittent claudication twice within 1 week prior to enrollment visit(Baseline is defined as the first measurement.Change from baseline in P-values less than or equal to 25%).
• Age:80 years old or younger.
• Intermittent claudication has been in stable condition in the last 6 months.And there was no history of exacerbations within 3 months prior to enrollment visit.
• Informed Consent:A signed and dated written informed consent prior to study participation.

Exclusion Criteria:

• Subjects who have cardiac disease including caradiac failure,arrhythmias,coronary disease,mitral or aortic stenosis.Subjects with a recent history of myocardial infarction within the past 6 months are to be excluded.
• Subjects who have pneumonedema,pulmonary infiltrates,interstitial pneumonia,severe chronic obstructive airway disorders or respiratory insufficiency confirmed by clinical examination.
• Liver:Subjects with abnormal liver function tests defined as aspartate aminotransferase(AST) or alanine aminotransferase(ALT) greater than equal to 1.5 times upper limit of normal,as well as a diagnosis of primary liver disease will be excluded.
• Renal:Subjects with abnormal kidney function tests defined as Creatinine clearance rate(SCr) greater than or equal to upper limit of normal.
• Clinically Uncontrolled Hypertension:Subjects who have clinically significant uncontrolled hypertension(Systolic blood pressure:greater than or equal to 180mmHg;Or diastolic blood pressure:greater than or equal to 110mmHg).
• Ankle systolic pressure is less than or equal to 50mmHg.
• Subjects with affected limbs surgery or endovascular treatment within 3 months prior to Screening.Subjects who received Prostanoids within the past 1 week are to be excluded.
• Subjects who received walking rehabilitation training successfully within the past 6 months.
• Subjects with a diagnosis of other diseases such as lower limb joint disorder,spinal lesions,neuropathy,serious lung and heart conditions which may impact intermittent claudication will be excluded.
• Subjects who have inflammation of the vascular disease including Takayasu's arteritis,edema perivascular.
• Subjects with active peptic ulcerease or bleeding tendency will be excluded.
• Glaucoma:Subjects with a diagnosis of glaucoma or high intraocular pressure will be excluded.
• Subjects who are medically unable to withhold their vasodilator including naftidrofuryl,pentoxy,buflomedil or cilostazol will be excluded.
• Subjects who received any powerful analgesic within 1 month perior to Screening.
• Subjects with a history of psychiatric disease or Alzheimer's Disease.
• Cancer:Subjects with a diagnosis of cancer will be excluded.
• Drug Allergy:Subjects who have a history of any componet of Alprostadil Injection.
• Previous Participation:Subjects who were previously enrolled in any clinical trial within 1 month period to Screening.
• Pregnancy:Women who are pregnant or lactating or women of childbearing potential who are not using an acceptable method of contraception.
• Subjects,who in the opinion of the Investigator,will not be fit for this study.