- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07574385
Sciatic Nerve Block With ALX006 in Subjects Undergoing Bunionectomy
4 maggio 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Reclutamento
Condizioni
Tipo di studio
Interventistico
Iscrizione (Stimato)
60
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Caleb Lade, MD
- Numero di telefono: 918-808-8399
- Email: caleb.lade@rebelmedicine.com
Luoghi di studio
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Utah
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Millcreek, Utah, Stati Uniti, 84107
- Reclutamento
- CenExel Salt Lake City
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Investigatore principale:
- Todd Bertoch, MD
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Contatto:
- Director of Clinical Operations
- Numero di telefono: (801) 261-2000
- Email: s.zunkowski@cenexel.com
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
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)
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: 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.
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ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
Altri nomi:
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Sperimentale: 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.
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ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
Altri nomi:
|
|
Sperimentale: 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
Altri nomi:
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Comparatore attivo: 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
Altri nomi:
Bupivacaine HCl 0.25% plain (2.5 mg/mL)
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidence and severity of treatment-emergent adverse events (TEAEs)
Lasso di tempo: 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
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From start of nerve block procedure through 360 Hour Visit (Day 15)
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
AUC of NRS pain intensity scores 0-72 hours post-surgery
Lasso di tempo: 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
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AUC of NRS pain intensity scores 0-96 hours post-surgery
Lasso di tempo: 0 to 96 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 96 hours post-surgery
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AUC of NRS pain intensity scores 0-120 hours post-surgery
Lasso di tempo: 0 to 120 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 120 hours post-surgery
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Total postsurgical opioid consumption in oral morphine equivalents (OMED) from 0 to 72 hours post-surgery
Lasso di tempo: 0 to 72 hours post-surgery
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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.
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0 to 72 hours post-surgery
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Total postsurgical opioid consumption in oral morphine equivalents (OMED) from 0 to 96 hours post-surgery
Lasso di tempo: 0 to 96 hours post-surgery
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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.
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0 to 96 hours post-surgery
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Total postsurgical opioid consumption in oral morphine equivalents (OMED) from 0 to 120 hours post-surgery
Lasso di tempo: 0 to 120 hours post-surgery
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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.
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0 to 120 hours post-surgery
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Percentage of opioid-free subjects through 72 hours post-surgery
Lasso di tempo: 0 to 72 hours post-surgery
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Proportion of subjects who consumed no opioid medication from the end of surgery through 72 hours.
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0 to 72 hours post-surgery
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Percentage of opioid-free subjects through 96 hours post-surgery
Lasso di tempo: 0 to 96 hours post-surgery
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Proportion of subjects who consumed no opioid medication from the end of surgery through 96 hours.
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0 to 96 hours post-surgery
|
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Percentage of opioid-free subjects through 120 hours post-surgery
Lasso di tempo: 0 to 120 hours post-surgery
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Proportion of subjects who consumed no opioid medication from the end of surgery through 120 hours.
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0 to 120 hours post-surgery
|
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Median time to first postsurgical opioid consumption
Lasso di tempo: End of surgery through 168 hours post-surgery
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Time from end of surgery to administration of the first postsurgical opioid dose.
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End of surgery through 168 hours post-surgery
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Plasma bupivacaine maximum observed concentration (Cmax)
Lasso di tempo: Pre-dose through 168 hours post-block administration
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Maximum observed plasma bupivacaine concentration following single-dose administration
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Pre-dose through 168 hours post-block administration
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Time to maximum plasma bupivacaine concentration (Tmax)
Lasso di tempo: Pre-dose through 168 hours post-block administration
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Time from end of block administration to the maximum observed plasma bupivacaine concentration.
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Pre-dose through 168 hours post-block administration
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Apparent terminal elimination half-life of bupivacaine (t½el)
Lasso di tempo: Pre-dose through 168 hours post-block administration
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Apparent terminal elimination half-life of plasma bupivacaine
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Pre-dose through 168 hours post-block administration
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Apparent clearance of bupivacaine (CL/F)
Lasso di tempo: Pre-dose through 168 hours post-block administration
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Apparent clearance of bupivacaine following perineural administration, derived by non-compartmental analysis.
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Pre-dose through 168 hours post-block administration
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Median time to onset of sensory block
Lasso di tempo: From end of block administration through 168 hours
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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
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From end of block administration through 168 hours
|
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Median duration of sensory block
Lasso di tempo: From end of block administration through 168 hours
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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.
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From end of block administration through 168 hours
|
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Median time to onset of motor block
Lasso di tempo: From end of block administration through 168 hours
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Median time from end of block administration to the earliest timepoint with partial or no foot movement
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From end of block administration through 168 hours
|
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Median duration of motor block
Lasso di tempo: From end of block administration through 168 hours
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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)
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From end of block administration through 168 hours
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Direttore dello studio: Jayant Agarwal, MD, Rebel Medicine Inc
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
10 marzo 2026
Completamento primario (Stimato)
1 agosto 2026
Completamento dello studio (Stimato)
1 agosto 2026
Date di iscrizione allo studio
Primo inviato
28 aprile 2026
Primo inviato che soddisfa i criteri di controllo qualità
4 maggio 2026
Primo Inserito (Effettivo)
7 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
7 maggio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
4 maggio 2026
Ultimo verificato
1 maggio 2026
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Manifestazioni neurologiche
- Malattie muscoloscheletriche
- Malattie del sistema nervoso
- Manifestazioni neurocomportamentali
- Disturbi percettivi
- Deformità del piede
- Condizioni patologiche, segni e sintomi
- Segni e sintomi
- Agnosi
- Alluce valgo
- Prodotti chimici organici
- Anilides
- Amides
- Composti di anilina
- Ammine
- Bupivacaina
Altri numeri di identificazione dello studio
- RBL-201
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Sì
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Alluce valgo
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Peking University Third HospitalNon ancora reclutamentoFascite plantare cronica | Limite Hallux funzionale