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Randomized, Double-blind, Placebo-controlled, Multicenter Phase IIb Clinical Trial of Spray YJ001 for the Treatment of Diabetic Peripheral Neuropathic Pain

2026年10月8日 更新者:Zhejiang Yuejia Pharmaceuticals Co., Ltd.

The goal of this clinical trial is to learn if YJ001 Spray can treat diabetic patients with Diabetic Peripheral Neuropathic Pain(DPNP). The main questions it aims to answer are:

  • Is YJ001 spray effective for patients with diabetic peripheral neuropathic pain(DPNP)?
  • The optimal effective dose of YJ001 spray for patients with diabetic peripheral neuropathic pain(DPNP).
  • Is YJ001 spray safe for patients with diabetic peripheral neuropathic pain(DPNP)? Researchers will divide YJ001 spray into three different doses of YJ001 spray and compare it with a placebo (a substance that looks similar but does not contain medication) to observe whether YJ001 spray can effectively treat diabetic peripheral neuropathic pain and to determine the optimal effective dose.

Participants will:

  • Apply spray topically to both feet twice daily, with six sprays per foot at each administration.Attend scheduled study visits at baseline and weeks 1, 2, 4, 8, and 12, followed by a visit 1 week after Treatment termination.
  • Record their symptoms and the number of times they use the spray.

調査の概要

研究の種類

介入

入学 (実際)

196

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Haidian District
      • Beijing、Haidian District、中国、100089
        • Peking University Third Hospital

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~75年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Male or female, between 18 to 75 years of age at screening
  • The subject is diagnosed with Type 1 or Type 2 diabetes with a disease duration of at least 1 year
  • The subject is diagnosed with diabetic peripheral neuropathic pain (DPNP, acceptable diagnostic certificates from other tertiary or higher-level hospitals.). Pain duration ≥ 3 months
  • Glycated hemoglobin level (HbA1c) ≤ 9%
  • At the screening visits, the score on the 11-point Numerical Rating Scale (NRS) must be ≥4.0. During the 1-week run-in period, subjects must complete at least 15 NRS scores, including 5 scores taken at 6 hours post-dose, and the mean pain score should have been ≥4.0
  • Subjects are willing and able to participate in study visits, treatment plans, laboratory tests, and other study procedures
  • Consented to participate in this study and signed the written informed consent form (ICF).

Exclusion Criteria:

  • Subjects who are known or suspected to be allergic to or have had severe adverse reactions to the ingredients of YJ001 , the ingredients of YJ001 placebos for spray use, aspirin, salicylic acid, or YJ001-like drugs (such as 5-aminosalicylic acid, sulfasalazine, and salicylate esters)
  • Subjects who participated in the YJ001 clinical study and received the investigational product before
  • Subjects had widespread systemic pain that could affect the evaluation of pain at the administration site, as judged by the investigator; or the pain in the hand or more proximal area is more severe than in the foot
  • Subjects with severe peripheral vascular disease (such as intermittent claudication) who were deemed by the investigator to be unsuitable for participation in the study at the time of screening
  • Subjects have pain caused by non-diabetic peripheral neuropathy, such as active osteoarthritis, stage II or higher peripheral arterial disease, lumbar disc herniation, vitamin B deficiency, alcoholism, herpes neuralgia, vasculitis, and the somatoform pain caused by psychological disorders such as severe depression and anxiety, which may affect the investigator's score for DPNP
  • Subjects had autoimmune diseases associated with elevated inflammatory factors at the time of screening, such as rheumatoid arthritis, inflammatory bowel disease, psoriasis, and atopic dermatitis
  • Presence of a skin disease in the skin area where the drug is administered, in the investigator's judgment, may affect the score for diabetic peripheral neuropathic pain; or the skin at the administration site is redness, inflamed, damaged, or otherwise affected in a way that may interfere with drug absorption; or, in the investigator's judgment, the subject has tattoos or other skin abnormalities that may interfere with the study objectives
  • The skin condition of the administration site scored >2
  • Malignant tumors, except for non-metastatic basal cell carcinoma or squamous cell carcinoma of the skin that has been appropriately treated or surgically removed, or in situ cervical cancer
  • Amputation of any part of the body other than the fingertips or toes
  • Combined with diabetes-related foot ulcers, infections, or gangrene
  • Acute diabetic metabolic complications, such as diabetic ketoacidosis, lactic acidosis, hyperosmolar hyperglycemic syndrome, or diabetic hyperosmolar coma
  • One or more episodes of severe hypoglycemia (defined as requiring assistance from others to obtain carbohydrates, glucagon, or other rescue measures) during the 6 months prior to screening or during the run-in period
  • During the one-week run-in period, the subject's NRS pain scores was <3 more than three times
  • Subjects who have used transcutaneous electrical nerve stimulation (TENS), acupuncture, or other therapeutic measures within two weeks prior to inclusion, or who require combined transcutaneous electrical nerve stimulation (TENS) or acupuncture treatment during the treatment period
  • Use of topical analgesics for the treatment of DPNP (such as capsaicin patches, lidocaine patches, etc.) within 2 weeks prior to inclusion
  • Abnormal liver and kidney function: aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 2.5 times the upper limit of normal values, creatinine > 1.5 times the upper limit of normal values
  • Combined severe cardiovascular and cerebrovascular diseases (such as second- or third-degree cardiac conduction block, heart failure classified as New York Heart Association (NYHA) Functional Classification III-IV, myocardial infarction, acute stroke, etc.)
  • Combined severe respiratory, blood, and hematopoietic system diseases
  • Subjects with other neurological disorders (such as cognitive impairment) that the investigator think it might affect the evaluation of diabetic peripheral neuropathic pain or self-assessment, or psychiatric patients who, in the investigator's judgment, are not suitable for participation in this trial
  • Subjects with a known or suspected history of alcohol abuse, drug abuse, or dependence within the past year
  • Pregnant or lactating women; male subjects (including their female partner) and female subjects of childbearing potential who plan to become pregnant or cannot guarantee the use of one or more contraceptive methods (common contraceptive methods include tubal ligation intrauterine devices, birth control pills, condoms, etc.) from the start of screening until three months after the end of the trial
  • Screen subjects who have participated in other clinical trials within the past 3 months
  • Other situations where the investigator considers it inappropriate to participate in this trial

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
プラセボコンパレーター:YJ001 spray simulator

YJ001 spray 0mg/ml,apply spray to both feet 0mg each time,twice daily, with six sprays per foot.

実験的:YJ001 Spray 240 mg/day

YJ001 spray 50mg/ml,apply spray to both feet 120mg each time,twice daily, with six sprays per foot.

実験的:YJ001 Spray 480 mg/day

YJ001 spray 100mg/ml,apply spray to both feet 240mg each time,twice daily, with six sprays per foot.

実験的:YJ001 Spray 960 mg/day

YJ001 spray 200mg/ml,apply spray to both feet 480mg each time,twice daily, with six sprays per foot

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change from baseline in weekly average Numeric Rating Scale (NRS) pain score at Week 12 after treatment.
時間枠:baseline and week 12

Numeric Rating Scale (NRS). This scale ranges from 0 to 10, with 0 representing no pain and 10 representing the worst imaginable pain. Higher scores indicate worse pain severity

baseline and week 12

二次結果の測定

結果測定
メジャーの説明
時間枠
Change from baseline in weekly average NRS pain scores during Week 1-11 after treatment and the follow-up period.
時間枠:baseline and weekly during Weeks 1-11

Numeric Rating Scale (NRS). This scale ranges from 0 to 10, with 0 representing no pain and 10 representing the worst imaginable pain. Higher scores indicate worse pain severity.

baseline and weekly during Weeks 1-11
Change from baseline in weekly average NRS pain scores measured 6 hours after morning dosing during Weeks 1-12 after treatment.
時間枠:baseline and 6 hours after morning dosing during Weeks 1-12

Numeric Rating Scale (NRS). This scale ranges from 0 to 10, with 0 representing no pain and 10 representing the worst imaginable pain. Higher scores indicate worse pain severity.

baseline and 6 hours after morning dosing during Weeks 1-12
Change from baseline in weekly average NRS pain scores before morning dosing during Week 1-12 after treatment.
時間枠:baseline,before morning dosing during Week 1-12

Numeric Rating Scale (NRS). This scale ranges from 0 to 10, with 0 representing no pain and 10 representing the worst imaginable pain. Higher scores indicate worse pain severity.

baseline,before morning dosing during Week 1-12
Change from baseline in weekly average NRS pain scores before evening dosing during Week 1-12 after treatment.
時間枠:baseline,before evening dosing during Week 1-12

Numeric Rating Scale (NRS). This scale ranges from 0 to 10, with 0 representing no pain and 10 representing the worst imaginable pain. Higher scores indicate worse pain severity.

baseline,before evening dosing during Week 1-12
Weekly responder rates (≥30 % and ≥50 % reduction) during Week 1-12 after treatment.
時間枠:Weekly during Week 1-12

Responder is defined as ≥30% or ≥50% reduction in weekly average Numeric Rating Scale (NRS) pain score from baseline. NRS: 0-10, 0=no pain,10=worst imaginable pain, higher scores mean worse pain.

Weekly during Week 1-12
Change from baseline in weekly average sleep interference scores during Week 1-12 after treatment and the follow-up period.
時間枠:baseline,Week 1, 2, 4, 8, 12

Weekly average sleep disturbance score. The scale ranges from 0 to 10. Higher scores indicate worse sleep disturbance.

baseline,Week 1, 2, 4, 8, 12
Change from baseline in Visual Analogue Scale (VAS) pain scores derived from the Short-form McGill Pain Questionnaire(SF-MPQ) at Week 1, 2, 4, 8, 12 after treatment and the follow-up period.
時間枠:baseline,Week 1, 2, 4, 8, 12

Short-Form McGill Pain Questionnaire Verbal Analogue Scale (SF-MPQ-VAS). The scale ranges from 0 to 10. Higher scores indicate worse pain.

baseline,Week 1, 2, 4, 8, 12
Change from baseline in Hospital Anxiety and Depression Scale (HADS) scores at Week 1, 2, 4, 8, 12 after treatment and the follow-up period.
時間枠:baseline,Week 1, 2, 4, 8, 12

Hospital Anxiety and Depression Scale (HADS). Total score ranges from 0 to 42. Higher scores indicate greater anxiety and depression symptoms.

baseline,Week 1, 2, 4, 8, 12
Patient's Global Impression of Change (PGIC) at Week 12 after treatment.
時間枠:Week 12

Patient Global Impression of Change (PGIC). The scale ranges from 1 to 7. Lower scores indicate better improvement in pain.

Week 12
Clinician's Global Impression of Change (CGIC) at Week 12 after treatment.
時間枠:Week 12

Clinician's Global Impression of Change (CGIC) is a 7-point clinician-rated scale. Scores range from 1 to 7: 1 = very much improved, 2 = much improved, 3 = minimally improved, 4 = no change, 5 = minimally worse, 6 = much worse, 7 = very much worse. Lower scores indicate better clinical improvement.

Week 12
Change from baseline in 36-Item Short-Form Health Survey (SF-36) scores at Week 12 after treatment.
時間枠:baseline and Week 12

Short Form-36 (SF-36) quality of life scale. Each domain score ranges from 0 to 100. Higher scores indicate better quality of life.

baseline and Week 12
Change from baseline in superficial peroneal and sural nerve conduction velocity and action potential amplitude at Week 12 after treatment.
時間枠:baseline,Week 12

Nerve conduction velocity and compound nerve action potential amplitude of superficial peroneal nerve and sural nerve will be measured by nerve conduction studies. The change from baseline in these electrophysiological parameters will be assessed at Week 12 after treatment. Higher nerve conduction velocity and higher amplitude indicate better nerve function.

baseline,Week 12
Change from baseline in serum tumour necrosis factor-α (TNF-α) level at Week 12 after treatment.
時間枠:baseline,Week 12

Serum tumour necrosis factor-α (TNF-α) concentration will be measured in blood samples. The change from baseline in serum TNF-α level will be evaluated at Week 12 after treatment. Lower TNF-α levels indicate reduced inflammatory status (better outcome).

baseline,Week 12
The self-assessed time for significant pain relief by subjects after treatment (defined as pain NRS score before morning or evening dosing reduction ≥30 % from baseline).
時間枠:before morning or evening dosing throughout the entire clinical trial period

This endpoint measures the self-assessed time to achieve significant pain relief by subjects. Significant pain relief is defined as a ≥30% reduction from baseline in the pre-morning or pre-evening dosing Numeric Rating Scale (NRS) pain score. The NRS ranges from 0 to 10, where 0 = no pain and 10 = worst imaginable pain. Higher scores indicate worse pain severity. The time to reach this pain relief threshold will be recorded throughout the trial.

before morning or evening dosing throughout the entire clinical trial period
Changes in NRS pain scores before morning dosing, 1, 3, 6, 9 hours after morning dosing, and before evening dosing within 3 days after significant relief of self-reported pain by the subjects
時間枠:before morning dosing, 1, 3, 6, 9 hours after morning dosing, and before evening dosing within 3 days after significant relief of self-reported pain by the subjects

This endpoint evaluates changes in subject-reported Numeric Rating Scale (NRS) pain scores. Assessments are collected at pre-morning dosing, 1, 3, 6, 9 hours after morning dosing, and pre-evening dosing within 3 days after subjects report significant pain relief. The NRS ranges from 0 to 10, where 0 = no pain and 10 = worst imaginable pain. Higher scores indicate worse pain severity.

before morning dosing, 1, 3, 6, 9 hours after morning dosing, and before evening dosing within 3 days after significant relief of self-reported pain by the subjects
Number of participants with clinically significant abnormal laboratory values
時間枠:Pre-import period,baseline,Week 4, 8, 12

Assessment of clinically significant abnormal laboratory values from hematology, serum biochemistry, coagulation and urinalysis tests. Laboratory panel includes hematology (RBC, Hb, WBC, NEU, PLT, NEU%, LYM%), serum biochemistry (AST, ALT, TBIL, GGT, ALP, DBIL, ALB, Scr, eGFR, HbA1c, FPG), coagulation (APTT, PT, TT, FIB, INR), urinalysis (PRO, GLU, LEU, UERY, urine pH).

Pre-import period,baseline,Week 4, 8, 12
Number of participants with clinically significant abnormal 12/18-lead ECG findings
時間枠:Pre-import period,baseline,Week 4, 8, 12

Assessment of clinically significant abnormal electrocardiogram (ECG) parameters from 12-lead or 18-lead ECG recordings, including heart rate, PR interval, QRS duration, QT interval, QTc interval, and morphological abnormalities.

Pre-import period,baseline,Week 4, 8, 12
Number of participants with respiratory tract irritation related to spray administration
時間枠:Week 1,2,4, 8, 12

Incidence of respiratory tract irritation adverse events occurring during spray administration, assessed via clinical inquiry and physical examination at each study visit.

Week 1,2,4, 8, 12
Any adverse events observed or reported throughout the study period will be documented promptly
時間枠:Pre-import period,baseline,Week 1,2, 4, 8, 12
Pre-import period,baseline,Week 1,2, 4, 8, 12
Change from baseline in serum interleukin (IL-6) level at Week 12 after treatment.
時間枠:baseline ,Week 12
baseline ,Week 12
Change from baseline in serum interleukin IL-1β level at Week 12 after treatment.
時間枠:baseline,week 12
baseline,week 12

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年1月18日

一次修了 (実際)

2024年12月27日

研究の完了 (実際)

2025年1月3日

試験登録日

最初に提出

2026年9月20日

QC基準を満たした最初の提出物

2026年9月28日

最初の投稿 (実際)

2026年10月5日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月15日

QC基準を満たした最後の更新が送信されました

2026年10月8日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • BOJI2023024YWX

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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