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Sciatic Nerve Block With ALX006 in Subjects Undergoing Bunionectomy

4 maja 2026 zaktualizowane przez: 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.

Przegląd badań

Typ studiów

Interwencyjne

Zapisy (Szacowany)

60

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Utah
      • Millcreek, Utah, Stany Zjednoczone, 84107
        • Rekrutacyjny
        • CenExel Salt Lake City
        • Główny śledczy:
          • Todd Bertoch, MD
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

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):

    1. History of liver cirrhosis, having an aspartate aminotransferase >3x the upper limit of normal (ULN), or having an alanine aminotransferase > 3x ULN.
    2. 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.
    3. 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 studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Zadanie sekwencyjne
  • Maskowanie: Poczwórny

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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
Inne nazwy:
  • Sciatic Nerve Block in the Popliteal Fossa
Eksperymentalny: 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
Inne nazwy:
  • Sciatic Nerve Block in the Popliteal Fossa
Eksperymentalny: 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
Inne nazwy:
  • Sciatic Nerve Block in the Popliteal Fossa
Aktywny komparator: 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
Inne nazwy:
  • Sciatic Nerve Block in the Popliteal Fossa
Bupivacaine HCl 0.25% plain (2.5 mg/mL)
Inne nazwy:
  • MARCAINE 0.25%

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Incidence and severity of treatment-emergent adverse events (TEAEs)
Ramy czasowe: 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)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
AUC of NRS pain intensity scores 0-72 hours post-surgery
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Median time to onset of sensory block
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Dyrektor Studium: Jayant Agarwal, MD, Rebel Medicine Inc

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

10 marca 2026

Zakończenie podstawowe (Szacowany)

1 sierpnia 2026

Ukończenie studiów (Szacowany)

1 sierpnia 2026

Daty rejestracji na studia

Pierwszy przesłany

28 kwietnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

4 maja 2026

Pierwszy wysłany (Rzeczywisty)

7 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

7 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

4 maja 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Paluch koślawy

Badania kliniczne na ALX006 (bupivacaine extended-release injection)

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