A Study to Evaluate the Efficacy and Safety of UI022/UI023
A Multi-Center, Randomized, Double-Blind, Parallel, Phase III Clinical Trial to Evaluate the Efficacy and Safety of UI022/UI023
調査の概要
状態
条件
研究の種類
入学 (実際)
段階
- フェーズ 3
連絡先と場所
研究場所
-
-
-
Seoul、韓国
- Yonsei University College of Medicine, Severance Hospital
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
Subjects must meet all of the following criteria.
Screening Inclusion Criteria
- Subjects aged 19 years or older.
- Subjects with lower limb ischemic symptoms persisting for at least 24 weeks before screening.
- Subjects who have been taking a statin according to dyslipidemia treatment guidelines for at least 12 weeks before screening.
- Subjects with stable symptoms without significant improvement during the 12 weeks before screening, with a response of 3 or less to KPAQ Question 3 and a KPAQ summary score of 60 or less.
- Subjects with ABI ≤ 0.9 at screening.Subjects with 0.9 < ABI ≤ 1.0 may participate if arterial stenosis of 50% or more is confirmed by vascular imaging.
- Subjects with Fontaine Stage II, including Stage IIa or IIb.
- Subjects who voluntarily provide written informed consent to participate in the clinical trial.
Randomization Inclusion Criteria
- Subjects whose KPAQ summary score differs by no more than 10% between the screening visit and baseline visit.
- Subjects who are able to maintain the dose of rosuvastatin, the run-in medication, during the treatment period.
- Subjects with compliance of 70% or higher with the run-in medication during the run-in period
Exclusion Criteria:
Subjects who meet any of the following criteria are not eligible to participate in this clinical trial.
- Subjects who underwent an endovascular procedure, surgery, or reconstruction within 24 weeks before the screening visit, or who are expected to require such a procedure, surgery, or reconstruction during the clinical trial.
- Subjects with any of the following medical histories at the screening visit:
1) Myocardial infarction, unstable angina, transient ischemic attack, stroke, coronary artery bypass graft, or coronary angioplasty within 12 weeks.
2) Deep vein thrombosis within 12 weeks. However, subjects with isolated calf vein thrombosis may participate.
3) Intolerance to statins, such as myopathy including rhabdomyolysis. 4) Malignant tumor within 5 years. 5) Alcohol or drug abuse. 3. Subjects with any of the following concomitant diseases at the screening visit:
- Moderate or severe lower limb pain caused by spinal disease, such as spinal stenosis.
- Congestive heart failure.
- Bleeding, including hemophilia, capillary fragility, intracranial hemorrhage, upper gastrointestinal bleeding, urinary tract bleeding, hemoptysis, or vitreous hemorrhage, or a bleeding tendency, including active peptic ulcer, hemorrhagic stroke within 24 weeks before screening, surgery within 12 weeks before screening, or proliferative diabetic retinopathy.
- Severe renal impairment, defined as Clcr < 30 mL/min.
- Uncontrolled diabetes mellitus, defined as HbA1c > 9%.
- Uncontrolled hypertension, defined as SBP > 180 mmHg or DBP > 110 mmHg.
- Abnormal muscle enzyme level, defined as CK > 3 times the upper limit of normal.
- Active liver disease, including unexplained persistent elevation of serum transaminases, ALT or AST, or elevation of serum transaminases greater than 3 times the upper limit of normal, ALT or AST > 3 times the upper limit of normal.
4. Subjects who have received cilostazol within 12 weeks before screening. 5. Subjects who are expected to require any of the following medications during the clinical trial:
Lipid-modifying agents other than rosuvastatin administered in this clinical trial, including statins, ezetimibe, bile acid sequestrants, nicotinic acid and its derivatives, and fibrates.
However, lipid-modifying agents other than statins are permitted if they have been administered at a stable dose without dose changes for at least 8 weeks from screening, or at least 12 weeks including the run-in period, and no dose change is expected during the clinical trial.
Antiplatelet agents, including aspirin, clopidogrel, dipyridamole, indobufen, prasugrel, sarpogrelate, triflusal, ticagrelor, and ticlopidine.
However, except for sarpogrelate and ticlopidine, antiplatelet agents are permitted if they have been administered at a stable dose without dose changes for at least 8 weeks from screening, or at least 12 weeks including the run-in period, and no dose change is expected during the clinical trial. Up to two antiplatelet agents other than the investigational product are permitted. If the investigator determines, based on the benefit-risk assessment of the treatment, that monotherapy with one antiplatelet agent or discontinuation is necessary in subjects receiving one or two antiplatelet agents, this may be permitted.
Anticoagulants, including heparin, low molecular weight heparin, warfarin, apixaban, dabigatran, edoxaban, and rivaroxaban.
However, non-vitamin K oral anticoagulants may be permitted if they have been administered at a stable dose without dose changes for at least 8 weeks from screening, or at least 12 weeks including the run-in period, and no dose change is expected during the clinical trial. Subjects receiving both a non-vitamin K oral anticoagulant and an antiplatelet agent are not eligible to participate.
- Thrombolytic agents, including streptokinase, tenecteplase, and urokinase.
- Prostaglandin E1 or I2 and their derivatives, including alprostadil, beraprost, iloprost, and limaprost.
- Other medications used for peripheral arterial disease, including pentoxifylline and Ginkgo biloba extract.
- Cyclosporine.
- Analgesics, including NSAIDs. However, concomitant use is permitted if analgesics are used transiently for the treatment of diseases other than the target clinical disease or for the treatment of adverse events.
6. Pregnant or lactating women, and women of childbearing potential or men who do not agree to use any of the following reliable contraceptive methods from screening until 30 days after the last dose of the investigational product:
- Implantation of an intrauterine device or intrauterine system.
- Sterilization of the subject or the subject's partner.
- Double-barrier method, including spermicide with condom and contraceptive diaphragm, vaginal sponge, or cervical cap.
7. Subjects who participated in another clinical trial and received or were treated with an investigational drug or medical device within 12 weeks before screening.
8. Subjects with known hypersensitivity or allergy to any component of the investigational product or to drugs of a similar class.
9. Subjects with hereditary problems such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption.
10. Subjects who are judged by the investigator to be ineligible to participate in the clinical trial for any other reason.
研究計画
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 |
|---|---|
|
実験的:Test group
UI022+UIC201804 or UI023+UIC201805
|
Run-in period: UIC201802 1 Tab/day + UIC201604 1 Tab/day, or UIC201803 1 Tab/day + UIC201801 1 Tab/day, for 4 weeks Treatment period: UI022 1 Tab/day + UIC201804 1 Tab/day, or UI023 1 Tab/day + UIC201805 1 Tab/day, for 24 weeks
|
|
アクティブコンパレータ:Control group
UIC201604+UIC201802 or UIC201801+UIC201803
|
Run-in period: UIC201802 1 Tab/day + UIC201604 1 Tab/day, or UIC201803 1 Tab/day + UIC201801 1 Tab/day, for 4 weeks Treatment period: UIC201604 1 Tab/day + UIC201802 1 Tab/day, or UIC201801 1 Tab/day + UIC201803 1 Tab/day, for 24 weeks
|
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 |
時間枠 |
|---|---|
|
Change From Baseline in KPAQ Summary Score at Week 24
時間枠:Baseline and Week 24
|
Baseline and Week 24
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Change From Baseline in KPAQ Summary Score at Weeks 4, 8, and 12
時間枠:Baseline, Week 4, Week 8, and Week 12
|
Baseline, Week 4, Week 8, and Week 12
|
|
Change From Baseline in KPAQ Domain Scores at Weeks 4, 8, 12, and 24
時間枠:Baseline, Week 4, Week 8, Week 12, and Week 24
|
Baseline, Week 4, Week 8, Week 12, and Week 24
|
|
Change From Baseline in 100-mm VAS Score for Lower Limb Pain at Weeks 4, 8, 12, and 24
時間枠:Baseline, Week 4, Week 8, Week 12, and Week 24
|
Baseline, Week 4, Week 8, Week 12, and Week 24
|
|
Improvement Rate of Lower Limb Ischemic Symptoms at Weeks 4, 8, 12, and 24
時間枠:Week 4, Week 8, Week 12, and Week 24
|
Week 4, Week 8, Week 12, and Week 24
|
|
Improvement of Lower Limb Ischemic Symptoms Based on Participant Global Assessment at Weeks 4, 8, 12, and 24
時間枠:Week 4, Week 8, Week 12, and Week 24
|
Week 4, Week 8, Week 12, and Week 24
|
|
Change From Baseline in Initial Claudication Distance Using the Treadmill Test at Weeks 12 and 24
時間枠:Baseline, Week 12, and Week 24
|
Baseline, Week 12, and Week 24
|
|
Change From Baseline in Functional Claudication Distance Using the Treadmill Test at Weeks 12 and 24
時間枠:Baseline, Week 12, and Week 24
|
Baseline, Week 12, and Week 24
|
|
Change From Baseline in Absolute Claudication Distance Using the Treadmill Test at Weeks 12 and 24
時間枠:Baseline, Week 12, and Week 24
|
Baseline, Week 12, and Week 24
|
|
Change From Baseline in Ankle-Brachial Index at Weeks 12 and 24
時間枠:Baseline, Week 12, and Week 24
|
Baseline, Week 12, and Week 24
|
|
Percent Change From Baseline in Lipid Parameters at Weeks 12 and 24
時間枠:Baseline, Week 12, and Week 24
|
Baseline, Week 12, and Week 24
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
末梢動脈疾患の臨床試験
-
HuidaGene Therapeutics Co., Ltd.募集
-
Hemab ApSPSI CRO募集フォン・ヴィレブランド病(VWD) | フォン・ヴィレブランド病 (VWD)、タイプ 1 | フォンウィルブランド病(VWD)、タイプ2 | Von Willebrand Disease(VWD)、タイプ3 | フォン・ウィルブランド病、タイプ2a | Von Willebrand病、タイプ2M | Von Willebrand病、タイプ2Nアメリカ, イギリス, オーストラリア
-
Adelphi Values LLCBlueprint Medicines Corporation完了肥満細胞性白血病 (MCL) | 攻撃的な全身性肥満細胞症 (ASM) | SM w Assoc Clonal Hema Non-mast Cell Lineage Disease (SM-AHNMD) | くすぶり全身性肥満細胞症 (SSM) | 無痛性全身性肥満細胞症 (ISM) ISM サブグループが完全に募集されましたアメリカ