| Eligibility |
Inclusion Criteria:
1. Written informed consent obtained before any trial-related activities voluntarily,
understanding the procedures and methods of this study, and be willing to strictly
follow the trial protocol;
2. Males or females, aged 18-75 years (both inclusive);
3. Diagnosed with type 1 or type 2 diabetes for more than 6 months, hemoglobin Alc
(HbA1c) between 7% and 10% at screening, fasting plasma glucose (FPG) <11.1 mmol/L,
and the glucose-lowering treatment has been stable for at least 30 days and is
expected to remain unchanged throughout the study;
4. According to the «China Type 2 Diabetes Prevention and Cure Guidelines (2020
edition)», those diagnosed with diabetic peripheral neuropathy are classified as
distal symmetric polyneuropathy (DSPN), the diagnostic criteria consists of:(1) A
clear history of diabetes; (2) Neuropathy appeared during or after diagnosis of
diabetes; (3) Symptoms and signs are consistent with the performance of DPN; (4)
Patients with clinical symptoms (pain, numbness, abnormal sensation, etc.), with
abnormality in any 1 of 5 examinations (ankle reflexes, needle pain, vibration,
pressure, temperature); Patients without symptoms, with abnormalities in any 2 of 5
examinations and a clinical diagnosis of DPN; (5) Excluding patients with neuropathy
caused by other causes;
5. Toronto Clinical Neuropathy Score (TCNS) = 6 points, with sensory test score = 2
points at screening and baseline.
Exclusion Criteria:
Those who meet any of the exclusion criteria will not be enrolled:
1. Patients with peripheral neuropathy caused by other diseases: such as cervical and
lumbar vertebral disease, cerebrovascular disease, intracranial tumor or trauma, toxic
peripheral neuropathy (e.g. chemotherapy, alcohol), Guillain-Barr é syndrome, multiple
sclerosis, bone joints or tendon lesions, severe arteriovenous and vascular lesions,
severe liver and kidney insufficiency, hyperthyroidism or degeneration, subclinical
thyroid dysfunction, vitamin B12 deficiency, infection (e.g. human immunodeficiency
virus), etc;
2. Patients with previous peripheral arterial disease, and significant intermittent
claudication symptoms or previous lower extremity vascular bypass or angioplasty at
screening;
3. History of malignant neoplasms (except cured basal cell skin cancer, in-situ
carcinomas and papillary thyroid cancer) or history of antineoplastic therapy within 5
years prior to screening;
4. Patients with a change of more than 2 points in the same item of the mTCNS at
screening and baseline;
5. Visual Analogue Scale (VAS) > 8 points at screening;
6. Diabetic foot, diabetic peripheral vascular lesions, lower limb amputation, diabetic
muscular atrophy, Charcot joint disease within 3 months prior to screening;
7. Acute complications such as severe hypoglycemia with loss of consciousness, diabetic
ketoacidosis, diabetic hyperosmolar hyperglycemia syndrome, lactic acidosis, etc.
within 3 months prior to screening;
8. Those who have used a prohibited combination drug within 3 months before screening
must discontinue the drug for at least 1 month or 5 half-lives (whichever is longer)
prior to screening visit, and the drug must be discontinued throughout the study
period;
9. Any of the following cardiovascular events within 6 months prior to screening:
unstable angina requiring hospitalization, myocardial infarction, coronary artery
bypass transplantation, transdermal coronary intervention (diagnostic angiography is
permitted), moderate to severe congestive heart failure (NYHA III or IV), atrial or
ventricular arrhythmia (e.g. atrial fibrillation, ventricular tachycardia, etc.)
requiring hospitalization, pacemaker or defibrillator implantation, temporary cerebral
ischemic attacks or cerebrovascular accidents (e.g. strokes); Or coronary artery
bypass grafting or revascularization is planned during the study;
10. Uncontrolled severe hypertension (untreated or post-treated) at screening, defined as
systolic blood pressure =160 mm Hg or diastolic blood pressure =100 mm Hg;
11. Those who with awake pulse < 60 BPM or > 100 BPM at screening;
12. The Body Mass Index (BMI) < 18.5 kg/m^2 or > 35 kg/m^2 at screening, calculated by BMI
= body weight (kg)/height^2(m^2);
13. Grade II or III atrioventricular block occurred in 12-lead ECG (in the absence of a
pacemaker) at screening, long QT syndrome or QTc > 450 ms (male) / 470 ms (female);
14. Any active infections at screening, including but not limited to urinary tract
infections, upper respiratory tract infections, diabetic foot infections, etc., and
who needs further treatment;
15. Severe hematologic, hepatic, or renal abnormalities at screening with any laboratory
assessments meeting the following criteria: 1)Platelet count < 100 × 10^9/L; 2)
Aspartate Aminotransferase (AST) or alanine aminotransferase (ALT) = 2.5 × upper limit
of normal (ULN) of the reference range, or total bilirubin = 1.5 × ULN of the
reference range; 3) Creatine kinase > 2.0 × ULN; 4) Estimated renal glomerular
Filtration Rate (eGFR) < 60 mL/(min*1.73m^2) (calculated using the CKD-EPI formula);
5) Triglycerides (TG) > 5.6 mmol/L;
16. HBsAg-positive with HBV DNA copy number above the lower limit of the HBV DNA test, or
HCV antibodies (HCV Ab)-positive with HCV RNA copy number above the lower limit of the
HCV RNA test, human immunodeficiency virus antibody (HIV Ab) positive, serum syphilis
helix antibody (TP Ab) positive with syphilis helix titrating positive at screening;
17. Thyroid dysfunction (FT3, FT4, TSH examination with clinically significant
abnormalities) at screening, including undergoing treatment;
18. Cannot swallow oral drugs, or suffer from diseases that affect oral drug absorption,
distribution, metabolism, excretion, as well as diseases that affect the evaluation of
the efficacy and safety of experimental drugs, such as active bowel disease, partial
or complete intestinal obstruction, chronic diarrhea, etc;
19. Patients who are allergic to any ingredient in the test drug;
20. Patients with severe bleeding disorders;
21. Conditions that may affect the evaluation of efficacy, such as skin diseases in the
affected skin area that may affect the evaluation of nerve conduction function;
22. Pregnancy, breast-feeding, the intention of becoming pregnant during the trial; or
women of childbearing potential (WOCBP) or male patient do not wish to use adequate
contraceptive measures from the time signing the informed consent form until 3 months
after the last dose of the study drug;
23. Patients who have a history of alcohol addiction or substance abuse prior to screening
(alcohol addiction is defined as regular daily alcohol consumption in excess of the
following standard amounts: 720 mL of beer, 300 mL of red wine or 90 mL of liquor,
approximately 20 g of alcohol) or an inability to limit alcohol consumption to this
standard throughout the study period;
24. Patients who have smoked more than 10 cigarettes (including 10 cigarettes) per day in
the three months before screening or who could not control less than 10 cigarettes per
day during the whole study period;
25. Participation in other trials within 3 months prior to screening;
26. Risk of incompliance and/or inability to complete the trial, as judged by the
investigator, including but not limited to: psychiatric disorder (such as eating
disorder), mental incapacity, unwillingness or evidence of uncooperative attitude,
language barriers precluding adequate understanding of the trial (including inability
to read or write);
27. Patient compliance < 80% or > 120% during the introductory period.
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