Postsurgical Analgesia After Unilateral Bunionectomy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of AMT-143 for Postsurgical Analgesia After Unilateral Bunionectomy
The study is designed to evaluate the safety, efficacy, and pharmacokinetics (PK) of two doses of AMT-143 in participants after unilateral bunionectomy.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ2
連絡先と場所
研究連絡先
研究連絡先
- 名前:Ab Khulbe
- 電話番号:416-360-2094
- メール:ab@amacathera.ca
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Ability and willingness to provide written informed consent, adhere to the study visit schedule, and complete all study assessments.
- Adults 18 to 75 years at screening.
- Planned distal metaphyseal osteotomy procedure (e.g., Austin procedure/chevron osteotomy) under general anesthesia.
- Health surgery rating according to American Society of Anesthesiologists (ASA) class 1-3.
- Body mass index (BMI) ≥18 and ≤39 kg/m^2.
Exclusion Criteria:
-
Surgery is for minimally invasive bunionectomy procedure.
-
Contralateral bunionectomy within 3 months of study dosing.
-
Planned surgical intervention concurrent with unilateral bunionectomy (e.g., collateral procedures).
-
Hypersensitivity/allergy to any ingredient in AMT-143 formulation (hyaluronan or methylcellulose).
-
History or presence of glucose-6-phosphate dehydrogenase deficiency.
-
History or presence of congenital or idiopathic methemoglobinemia.
-
Hypersensitivity/allergy to amide type local anaesthetics (e.g., lidocaine, bupivacaine, ropivacaine, etc.).
-
Loss of sensation or significant peripheral neuropathy on the side of bunionectomy.
-
Concurrent pain syndromes (e.g., arthritis, fibromyalgia, cancer, etc.) that would require an additional use of non-steroidal anti-inflammatory drugs (NSAIDs), acetaminophen, or opioids during the course of the study.
-
Arrhythmias predisposing to long QT syndrome (e.g., ventricular tachycardia, atrial fibrillation, atrioventricular block, etc.).
-
Disease or condition that in the opinion of the Investigator, would pose a health risk to the participant or interfere with study assessments or compliance, including but not limited to, any of the following:
- Myocardial infarction within 6 months of study dosing or coronary bypass grafting within 12 months of study dosing.
- Congestive heart failure (New York Heart Association Class III-IV).
- Uncontrolled diabetes with A1C hemoglobin ≥ 7%.
- Severe peripheral vascular disease.
- Pulmonary dysfunction.
- Severe hepatic or renal dysfunction.
- Coagulation or bleeding disorders.
- Uncontrolled anxiety, schizophrenia, or other psychiatric disorders.
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Have history of human immunodeficiency virus (HIV) or hepatitis B/hepatitis C or a positive test at screening.
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Suspected or known addiction or abuse of illicit drugs, prescription medications, or alcohol within 2 years of study.
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Administration of an investigational drug within 30 days or 5 elimination half-lives of such investigational drug, whichever is longer, prior to study dosing, or planned administration of another investigational drug or procedure during the subject's participation in this study.
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Administration of medications with a potential for drug interactions with ropivacaine (i.e., amide-type local anaesthetics such as lidocaine, bupivacaine, mepivacaine and prilocaine; antiarrhythmics such as procainamide, disopyramide, tocainide, mexiletine and flecainide; inhibitors of cytochrome P4501A2 such as fluvoxamine and enoxacin) for at least 5 half-lives prior to study dosing.
-
Current use of neuromodulating agents [e.g., gabapentin, pregabalin (Lyrica), duloxetine (Cymbalta), etc.].
-
Use of systemic glucocorticoids within 30 days of study dosing.
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Use of dexmedetomidine HCl (Precedex®) or clonidine within 3 days of study dosing.
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Chronic opioid use [average ≥30 oral morphine equivalents (OMEDs)/day] within 30 days of study dosing.
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Use of opioid medications within 3 days of study dosing.
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Use of marijuana, tetrahydrocannabinol (THC), and cannabidiol (CBD) within 30 days of study dosing or planned use during the course of the study.
-
Current pregnancy, nursing, or planning to become pregnant during the study.
-
Unwillingness to use effective methods of contraception during participation in this study (for females with childbearing potential and males).
-
Recent or potential exposure to COVID-19.
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:支持療法
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:トリプル
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
プラセボコンパレーター:生理食塩水プラセボ
|
Group 3 will receive 2.00 mL Placebo [sodium chloride (NaCl) 0.9%]. |
|
実験的:AMT-143 Group 1
|
Group 1 will receive AMT-143 containing 354 mg ropivacaine. Group 2 will receive AMT-143 containing 707 mg ropivacaine. |
|
実験的:AMT-143 Group 2
|
Group 1 will receive AMT-143 containing 354 mg ropivacaine. Group 2 will receive AMT-143 containing 707 mg ropivacaine. |
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Safety and Tolerability of AMT-143
時間枠:From surgery to Day 28 follow-up
|
To evaluate the safety and tolerability of AMT-143 in participants undergoing unilateral bunionectomy. The primary safety endpoint is the incidence of treatment emergent adverse events (TEAEs), serious adverse events (SAEs), and adverse events of special interest (AESIs) which reflect manifestations of local anesthetic (ropivacaine) systemic toxicity (LAST). |
From surgery to Day 28 follow-up
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Analgesic Efficacy of AMT-143
時間枠:From surgery to Day 28 follow-up
|
To evaluate efficacy of AMT-143 for postsurgical pain management following unilateral bunionectomy. Numeric Rating Scale (NRS) pain intensity will be assessed while the participant is seated/recumbent with the surgically attended leg elevated or lying supine. The participant will be asked to rate their pain intensity on a scale of 0 to 10, where 0 = no pain and 10 = worst pain. |
From surgery to Day 28 follow-up
|
|
Area under the plasma concentration-versus-time curve (AUC)
時間枠:From surgery to Day 28 follow-up
|
From surgery to Day 28 follow-up
|
|
|
Maximum observed plasma concentration (Cmax)
時間枠:From surgery to Day 28 follow-up
|
From surgery to Day 28 follow-up
|
|
|
Time of maximum observed plasma concentration (Tmax)
時間枠:From surgery to Day 28 follow-up
|
From surgery to Day 28 follow-up
|
|
|
Apparent terminal elimination half-life (t1/2)
時間枠:From surgery to Day 28 follow-up
|
From surgery to Day 28 follow-up
|
|
|
Apparent clearance (CL)
時間枠:From surgery to Day 28 follow-up
|
From surgery to Day 28 follow-up
|
|
|
Apparent volume of distribution (Vd)
時間枠:From surgery to Day 28 follow-up
|
From surgery to Day 28 follow-up
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
その他の研究ID番号
- AMT-143-004
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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
米国FDA規制機器製品の研究
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