Sciatic Nerve Block With ALX006 in Subjects Undergoing Bunionectomy
2026年5月4日 更新者:Rebel Medicine Inc
A Phase 2, Randomized, Double-blind, Active-controlled, Dose-escalation Study to Evaluate the Safety, Pharmacokinetics, Efficacy and Pharmacodynamics of ALX006 for Postsurgical Pain Management When Administered as a Sciatic (in the Popliteal Fossa) Nerve Block in Subjects Undergoing a Bunionectomy
This is a Phase 2, randomized, double-blind, active-controlled, dose-escalation study evaluating the safety, pharmacokinetics, efficacy, and pharmacodynamics of ALX006, an extended-release bupivacaine formulation, administered as a single-dose sciatic nerve block in the popliteal fossa in adult subjects undergoing primary unilateral bunionectomy.
Approximately 60 subjects will be enrolled across 3 sequential dose cohorts (100 mg, 150 mg, 200 mg ALX006), with each cohort comparing ALX006 against MARCAINE 0.25% (bupivacaine HCl 50 mg) as the active comparator at a 3:1 randomization ratio.
Dose escalation between cohorts is governed by an Independent Data Monitoring Committee.
研究概览
地位
招聘中
研究类型
介入性
注册 (估计的)
60
阶段
- 阶段2
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Caleb Lade, MD
- 电话号码:918-808-8399
- 邮箱:caleb.lade@rebelmedicine.com
学习地点
-
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Utah
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Millcreek、Utah、美国、84107
- 招聘中
- CenExel Salt Lake City
-
首席研究员:
- Todd Bertoch, MD
-
接触:
- Director of Clinical Operations
- 电话号码:(801) 261-2000
- 邮箱:s.zunkowski@cenexel.com
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Male or female, ages 18 or older at screening
- American Society of Anesthesiologists (ASA) physical status 1, 2, or 3 (see Appendix 5)
- Able to provide informed consent, adhere to the study schedule, and complete all study assessments
- Primary surgical indication is related to a bunion deformity (i.e., hallux valgus) and subject is scheduled to undergo a primary unilateral distal metaphyseal osteotomy procedure (i.e., Austin procedure)
- Indicated to undergo elective (i.e., not emergency) bunionectomy
- Body Mass Index (BMI) ≥18 and <40 kg/m2
Exclusion Criteria:
- Allergy, hypersensitivity, intolerance, or contraindication to any of the study medications for which an alternative is not named in the protocol (e.g., amide-type local anesthetics, opioids, bupivacaine HCl, NSAIDs)
- Concurrent painful physical condition (e.g. arthritis, fibromyalgia, cancer) that may require analgesic treatment with NSAIDs or opioids in the post dosing period for pain that is not strictly related to the surgery and which, in the Investigator's opinion, may confound the post dosing assessments
- Inadequate sensory function of the foot/ankle as assessed by the Investigator
- History of, suspected, or known addiction to or abuse of illicit drug(s), prescription medicine(s), or alcohol within the past two (2) years
- Administration of an investigational drug within thirty (30) days or five (5) elimination half-lives of such investigational drug, whichever is longer, prior to study drug administration, or planned administration of another investigational product or procedure during the subject's participation in this study
- Administration of any local anesthetic within 72 hours prior to administration of study drug, other than for pretreatment prior to a needle placement
- Require additional local anesthetic other than study drug or lidocaine used for the Mayo field block or for pretreatment prior to a needle placement during the study period
- Uncontrolled anxiety, psychiatric, or neurological disorder that, in the opinion of the Investigator, could interfere with study assessments or compliance
- Currently pregnant, nursing, or planning to become pregnant during the study
- Clinically significant medical disease that, in the opinion of the Investigator would make participation in a clinical study inappropriate. This includes diabetic neuropathy, coagulation or bleeding disorders, severe peripheral vascular disease, renal insufficiency, hepatic dysfunction, glucose-6-phosphate dehydrogenase deficiency or other conditions that would constitute a contraindication to participation in the study
- Confirmed clinically significant vital sign or ECG abnormality, including QTcF > 450 msec at Screening
Has any of the following laboratory abnormalities during Screening (1 retest permitted):
- History of liver cirrhosis, having an aspartate aminotransferase >3x the upper limit of normal (ULN), or having an alanine aminotransferase > 3x ULN.
- Severe kidney function impairment as defined by estimated glomerular filtration rate (eGFR) by CKD-EPI 2021 equation <30 mL/min/1.73 m²or on dialysis.
- Platelet count < 100,000/uL, hemoglobin < 12 g/dL, or hematocrit < 35%.
- Currently on a gabapentinoid (e.g., gabapentin, pregabalin [Lyrica]) or a serotonin-norepinephrine reuptake inhibitor (SNRI) with recognized analgesic properties (e.g., duloxetine [Cymbalta]) that cannot be discontinued within 30 days before surgery. Other agents with documented efficacy in modulating acute or chronic pain may be excluded at the discretion of the Investigator in consultation with the Sponsor Medical Monitor. Selective serotonin reuptake inhibitors (SSRIs) are not excluded under this criterion.
- Current use of systemic glucocorticoids within thirty (30) days of randomization in this study
- Use of dexmedetomidine HCl or clonidine within three (3) days of study drug administration
- Any use of marijuana (including tetrahydrocannabinol (THC) and cannabidiol (CBD)) within thirty (30) days prior to randomization, or planned use during the study.
- Chronic opioid use within thirty (30) days prior to randomization (average ≥30 oral morphine mg equivalents/day)
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:顺序分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:ALX006 100 mg
Single-dose ALX006 100 mg (50 mg/mL bupivacaine free base) administered as ultrasound-guided sciatic nerve block in the popliteal fossa, 60 min (±15 min) prior to bunionectomy.
|
ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
其他名称:
|
|
实验性的:ALX006 150 mg
Single-dose ALX006 150 mg (50 mg/mL bupivacaine free base) administered as ultrasound-guided sciatic nerve block in the popliteal fossa, 60 min (±15 min) prior to bunionectomy.
|
ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
其他名称:
|
|
实验性的:ALX006 200 mg
Single-dose ALX006 200 mg (50 mg/mL; bupivacaine free base) administered as ultrasound-guided sciatic nerve block in the popliteal fossa, 60 min (±15 min) prior to bunionectomy.
|
ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
其他名称:
|
|
有源比较器:MARCAINE 0.25%
Single-dose MARCAINE 0.25% (bupivacaine HCl 50 mg; 20 mL), administered as ultrasound-guided sciatic nerve block in the popliteal fossa, 60 min (±15 min) prior to bunionectomy.
|
Sciatic nerve block in the popliteal fossa
其他名称:
Bupivacaine HCl 0.25% plain (2.5 mg/mL)
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Incidence and severity of treatment-emergent adverse events (TEAEs)
大体时间:From start of nerve block procedure through 360 Hour Visit (Day 15)
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TEAEs graded by CTCAE v5.0, summarized by System Organ Class and Preferred Term
|
From start of nerve block procedure through 360 Hour Visit (Day 15)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
AUC of NRS pain intensity scores 0-72 hours post-surgery
大体时间:0 to 72 hours post-surgery
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Area under the curve of 11-point Numeric Rating Scale (0 = no pain; 10 = worst possible pain) for current pain in operative foot
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0 to 72 hours post-surgery
|
|
AUC of NRS pain intensity scores 0-96 hours post-surgery
大体时间:0 to 96 hours post-surgery
|
Area under the curve of 11-point Numeric Rating Scale (0 = no pain; 10 = worst possible pain) for current pain in operative foot
|
0 to 96 hours post-surgery
|
|
AUC of NRS pain intensity scores 0-120 hours post-surgery
大体时间:0 to 120 hours post-surgery
|
Area under the curve of 11-point Numeric Rating Scale (0 = no pain; 10 = worst possible pain) for current pain in operative foot
|
0 to 120 hours post-surgery
|
|
Total postsurgical opioid consumption in oral morphine equivalents (OMED) from 0 to 72 hours post-surgery
大体时间:0 to 72 hours post-surgery
|
Cumulative opioid consumption from the end of surgery through 72 hours, calculated as oral morphine equivalent dose (OMED) using CDC opioid morphine equivalent conversion factors.
|
0 to 72 hours post-surgery
|
|
Total postsurgical opioid consumption in oral morphine equivalents (OMED) from 0 to 96 hours post-surgery
大体时间:0 to 96 hours post-surgery
|
Cumulative opioid consumption from the end of surgery through 96 hours, calculated as oral morphine equivalent dose (OMED) using CDC opioid morphine equivalent conversion factors.
|
0 to 96 hours post-surgery
|
|
Total postsurgical opioid consumption in oral morphine equivalents (OMED) from 0 to 120 hours post-surgery
大体时间:0 to 120 hours post-surgery
|
Cumulative opioid consumption from the end of surgery through 120 hours, calculated as oral morphine equivalent dose (OMED) using CDC opioid morphine equivalent conversion factors.
|
0 to 120 hours post-surgery
|
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Percentage of opioid-free subjects through 72 hours post-surgery
大体时间:0 to 72 hours post-surgery
|
Proportion of subjects who consumed no opioid medication from the end of surgery through 72 hours.
|
0 to 72 hours post-surgery
|
|
Percentage of opioid-free subjects through 96 hours post-surgery
大体时间:0 to 96 hours post-surgery
|
Proportion of subjects who consumed no opioid medication from the end of surgery through 96 hours.
|
0 to 96 hours post-surgery
|
|
Percentage of opioid-free subjects through 120 hours post-surgery
大体时间:0 to 120 hours post-surgery
|
Proportion of subjects who consumed no opioid medication from the end of surgery through 120 hours.
|
0 to 120 hours post-surgery
|
|
Median time to first postsurgical opioid consumption
大体时间:End of surgery through 168 hours post-surgery
|
Time from end of surgery to administration of the first postsurgical opioid dose.
|
End of surgery through 168 hours post-surgery
|
|
Plasma bupivacaine maximum observed concentration (Cmax)
大体时间:Pre-dose through 168 hours post-block administration
|
Maximum observed plasma bupivacaine concentration following single-dose administration
|
Pre-dose through 168 hours post-block administration
|
|
Time to maximum plasma bupivacaine concentration (Tmax)
大体时间:Pre-dose through 168 hours post-block administration
|
Time from end of block administration to the maximum observed plasma bupivacaine concentration.
|
Pre-dose through 168 hours post-block administration
|
|
Apparent terminal elimination half-life of bupivacaine (t½el)
大体时间:Pre-dose through 168 hours post-block administration
|
Apparent terminal elimination half-life of plasma bupivacaine
|
Pre-dose through 168 hours post-block administration
|
|
Apparent clearance of bupivacaine (CL/F)
大体时间:Pre-dose through 168 hours post-block administration
|
Apparent clearance of bupivacaine following perineural administration, derived by non-compartmental analysis.
|
Pre-dose through 168 hours post-block administration
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Median time to onset of sensory block
大体时间:From end of block administration through 168 hours
|
Median time from end of block administration to the earliest timepoint with loss of light touch sensation along the distribution of the target nerve distal to the block site
|
From end of block administration through 168 hours
|
|
Median duration of sensory block
大体时间:From end of block administration through 168 hours
|
Median time between onset and offset of sensory block, where offset is defined as the first timepoint of return of light touch sensation in both test areas in a single assessment.
|
From end of block administration through 168 hours
|
|
Median time to onset of motor block
大体时间:From end of block administration through 168 hours
|
Median time from end of block administration to the earliest timepoint with partial or no foot movement
|
From end of block administration through 168 hours
|
|
Median duration of motor block
大体时间:From end of block administration through 168 hours
|
Median time between onset and offset of motor block, where offset is defined as resolution of motor block with complete foot movement (dorsiflexion and plantar flexion)
|
From end of block administration through 168 hours
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 研究主任:Jayant Agarwal, MD、Rebel Medicine Inc
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年3月10日
初级完成 (估计的)
2026年8月1日
研究完成 (估计的)
2026年8月1日
研究注册日期
首次提交
2026年4月28日
首先提交符合 QC 标准的
2026年5月4日
首次发布 (实际的)
2026年5月7日
研究记录更新
最后更新发布 (实际的)
2026年5月7日
上次提交的符合 QC 标准的更新
2026年5月4日
最后验证
2026年5月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.