Sciatic Nerve Block With ALX006 in Subjects Undergoing Bunionectomy
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
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Typ studiów
Typ studiów
Zapisy (Szacowany)
Zapisy
Faza
Faza
- Faza 2
Kontakty i lokalizacje
Kontakt w sprawie studiów
Kontakt w sprawie studiów
- Nazwa: Caleb Lade, MD
- Numer telefonu: 918-808-8399
- E-mail: caleb.lade@rebelmedicine.com
Lokalizacje studiów
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Utah
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Millcreek, Utah, Stany Zjednoczone, 84107
- Rekrutacyjny
- CenExel Salt Lake City
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Główny śledczy:
- Todd Bertoch, MD
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Kontakt:
- Director of Clinical Operations
- Numer telefonu: (801) 261-2000
- E-mail: s.zunkowski@cenexel.com
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Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
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):
- 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 studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Zadanie sekwencyjne
- Maskowanie: Poczwórny
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
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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.
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ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
Inne nazwy:
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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.
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ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
Inne nazwy:
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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.
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ALX006 (50 mg/mL bupivacaine free base)
Sciatic nerve block in the popliteal fossa
Inne nazwy:
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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.
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Sciatic nerve block in the popliteal fossa
Inne nazwy:
Bupivacaine HCl 0.25% plain (2.5 mg/mL)
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Incidence and severity of treatment-emergent adverse events (TEAEs)
Ramy czasowe: 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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Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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AUC of NRS pain intensity scores 0-72 hours post-surgery
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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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Inne miary wyników
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Median time to onset of sensory block
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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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Współpracownicy i badacze
Sponsor
Sponsor
Śledczy
Śledczy
- Dyrektor Studium: Jayant Agarwal, MD, Rebel Medicine Inc
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Objawy neurologiczne
- Choroby układu mięśniowo-szkieletowego
- Choroby Układu Nerwowego
- Manifestacje neurobehawioralne
- Zaburzenia percepcyjne
- Deformacje stóp
- Stany patologiczne, oznaki i objawy
- Objawy i symptomy
- Agnozja
- Paluch koślawy
- Organiczne chemikalia
- Anilidy
- Amides
- Związki aniliny
- Aminy
- Bupiwakaina
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- RBL-201
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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