- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07574385
Sciatic Nerve Block With ALX006 in Subjects Undergoing Bunionectomy
4 mai 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Recrutement
Les conditions
Type d'étude
Interventionnel
Inscription (Estimé)
60
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Caleb Lade, MD
- Numéro de téléphone: 918-808-8399
- E-mail: caleb.lade@rebelmedicine.com
Lieux d'étude
-
-
Utah
-
Millcreek, Utah, États-Unis, 84107
- Recrutement
- CenExel Salt Lake City
-
Chercheur principal:
- Todd Bertoch, MD
-
Contact:
- Director of Clinical Operations
- Numéro de téléphone: (801) 261-2000
- E-mail: s.zunkowski@cenexel.com
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
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)
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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
Autres noms:
|
|
Expérimental: 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
Autres noms:
|
|
Expérimental: 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
Autres noms:
|
|
Comparateur actif: 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
Autres noms:
Bupivacaine HCl 0.25% plain (2.5 mg/mL)
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Incidence and severity of treatment-emergent adverse events (TEAEs)
Délai: From start of nerve block procedure through 360 Hour Visit (Day 15)
|
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)
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
AUC of NRS pain intensity scores 0-72 hours post-surgery
Délai: 0 to 72 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 72 hours post-surgery
|
|
AUC of NRS pain intensity scores 0-96 hours post-surgery
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
|
|
Percentage of opioid-free subjects through 72 hours post-surgery
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Median time to onset of sensory block
Délai: 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
Délai: 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
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Directeur d'études: Jayant Agarwal, MD, Rebel Medicine Inc
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
10 mars 2026
Achèvement primaire (Estimé)
1 août 2026
Achèvement de l'étude (Estimé)
1 août 2026
Dates d'inscription aux études
Première soumission
28 avril 2026
Première soumission répondant aux critères de contrôle qualité
4 mai 2026
Première publication (Réel)
7 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
7 mai 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
4 mai 2026
Dernière vérification
1 mai 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Manifestations neurologiques
- Maladies musculo-squelettiques
- Maladies du système nerveux
- Manifestations neurocomportementales
- Troubles de la perception
- Déformations du pied
- Conditions pathologiques, signes et symptômes
- Signes et symptômes
- Agnosie
- Hallux valgus
- Produits chimiques organiques
- Anilides
- Amides
- Composés aniline
- Amines
- Bupivacaïne
Autres numéros d'identification d'étude
- RBL-201
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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