- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07574385
Sciatic Nerve Block With ALX006 in Subjects Undergoing Bunionectomy
4. Mai 2026 aktualisiert von: 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.
Studienübersicht
Status
Rekrutierung
Bedingungen
Studientyp
Interventionell
Einschreibung (Geschätzt)
60
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Caleb Lade, MD
- Telefonnummer: 918-808-8399
- E-Mail: caleb.lade@rebelmedicine.com
Studienorte
-
-
Utah
-
Millcreek, Utah, Vereinigte Staaten, 84107
- Rekrutierung
- CenExel Salt Lake City
-
Hauptermittler:
- Todd Bertoch, MD
-
Kontakt:
- Director of Clinical Operations
- Telefonnummer: (801) 261-2000
- E-Mail: s.zunkowski@cenexel.com
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
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)
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Sequenzielle Zuweisung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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
Andere Namen:
|
|
Experimental: 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
Andere Namen:
|
|
Experimental: 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
Andere Namen:
|
|
Aktiver 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
Andere Namen:
Bupivacaine HCl 0.25% plain (2.5 mg/mL)
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Incidence and severity of treatment-emergent adverse events (TEAEs)
Zeitfenster: 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)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
AUC of NRS pain intensity scores 0-72 hours post-surgery
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Median time to onset of sensory block
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Studienleiter: Jayant Agarwal, MD, Rebel Medicine Inc
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
10. März 2026
Primärer Abschluss (Geschätzt)
1. August 2026
Studienabschluss (Geschätzt)
1. August 2026
Studienanmeldedaten
Zuerst eingereicht
28. April 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
4. Mai 2026
Zuerst gepostet (Tatsächlich)
7. Mai 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
7. Mai 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
4. Mai 2026
Zuletzt verifiziert
1. Mai 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Neurologische Manifestationen
- Erkrankungen des Bewegungsapparates
- Erkrankungen des Nervensystems
- Neurobehaviorale Manifestationen
- Wahrnehmungsstörungen
- Fußdeformitäten
- Pathologische Zustände, Anzeichen und Symptome
- Anzeichen und Symptome
- Agnosie
- Hallux Valgus
- Organische Chemikalien
- Anilides
- Amides
- Anilinverbindungen
- Amine
- Bupivacain
Andere Studien-ID-Nummern
- RBL-201
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Ja
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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-
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-
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