Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Une étude pharmacocinétique ouverte des formulations ASP-001 chez des volontaires sains

2 octobre 2026 mis à jour par: Aspartes Pharmaceuticals, Inc.

Une étude de phase 1, randomisée, en ouvert, à dose unique, à cinq voies en cross-over pour comparer la pharmacocinétique des comprimés orodispersibles Asp-001, 2 mg et 5 mg (formulations A et B) avec le comprimé Sibelium® 5 mg chez des participants en bonne santé

This study will assess the pharmacokinetics (PKs), safety and tolerability of ASP-001 in healthy volunteers. ASP-001 is an orally disintegrating tablet (ODT) formulation of flunarizine. This study will assess two formulations, Formulation A and Formulation B, at dose levels of 2 and 5 mg compared to the reference product, the Sibelium brand of flunarizine 5 mg tablet.

Whilst this is not a first-in-human (FIH) study of flunarizine, which is available in countries outside of Australia and has been studied extensively, it is a FIH study of ASP-001. In this open-label study, 12 participants will be assigned to one of five dosing sequences, in which they will receive a single dose of ASP-001 or Sibelium 5 mg in five separate dosing periods. The study drugs will be:

  • Treatment A: ASP-001 Formulation A, 5 mg
  • Treatment B: ASP-001 Formulation A, 2 mg
  • Treatment C: ASP-001 Formulation B, 5 mg
  • Treatment D: ASP-001 Formulation B, 2 mg
  • Treatment E: Sibelium, 5 mg Each dosing period will be separated by at least a 7-day washout period after the day of dosing. Approximately 14 days after the fifth and final dosing day, participants will return to the site to complete their end of study assessments.

Aboriginal and Torres Strait Islander participants will not be targeted directly; however, they will be permitted to be on-study if they meet all of the eligibility criteria. Participants under the age of 18 will not be permitted on study.

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Réel)

11

Phase

  • La phase 1

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.

Lieux d'étude

    • Western Australia
      • Nedlands, Western Australia, Australie, 6009
        • Linear Early Phase Limited

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

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Male or female, ≥18 and ≤65 years of age at screening, with body mass index (BMI) ≥18.5 and ≤32.0 kg/m2 and body weight ≥50.0 kg for males and ≥45.0 kg for females.

  2. Healthy as defined by:

    1. the absence of clinically significant illness and surgery (including abdominal or gastrointestinal surgery that may alter drug absorption) within 4 weeks prior to dosing.
    2. the absence of clinically significant history of neurological (including Parkinson's disease or other extrapyramidal disorders), endocrine, cardiovascular, respiratory, hematological, immunological, psychiatric (including depression), gastrointestinal, renal, hepatic, and metabolic disease.
  3. Non smoker, defined as no use of tobacco or nicotine containing products (including cigarettes, e cigarettes, cigars, pipes, or smokeless tobacco) for at least 6 months prior to screening.

  4. Female participants of non-childbearing potential must be:

    1. post-menopausal (spontaneous amenorrhea for at least 12 months prior to dosing) with confirmation by documented follicle stimulating hormone (FSH) levels ≥40 mIU/mL; or
    2. surgically sterile (bilateral oophorectomy, bilateral salpingectomy, or hysterectomy) or having had a tubal ligation performed at least 3 months prior to dosing.
  5. Sexually active female participants of childbearing potential and non-sterile male participants must be willing to use an acceptable contraceptive method throughout the study as detailed in section 7.1.

  6. Willing to take off dentures or mouth piercing at the time of dosing.

  7. Able to understand the study procedures and provide signed informed consent to participate in the study.

Exclusion Criteria:

  1. Any clinically significant abnormal finding at physical examination at screening.

  2. PHQ-9 score > 10 at screening or baseline (Day -1).

  3. Clinically significant abnormal laboratory test results or positive serology test results for HBsAg, HCV antibody, or HIV antigen and antibody at screening. Any abnormalities or deviations outside the normal ranges for any clinical laboratory testing can be repeated once at the discretion of the investigator and/or designee.

  4. Any of the following laboratory parameters above 1.5× upper limit of normal (ULN) at screening or baseline (Day -1): AST, ALT, direct bilirubin, indirect bilirubin, and total bilirubin. Values over 1.5× ULN may be repeated once for confirmation if the investigator considers it reasonable (e.g., potential elevation due to recent strenuous physical activity).

  5. History of clinically significant liver disease, impaired synthetic liver function, or jaundice. Resolved childhood jaundice is not exclusionary.

  6. Value of creatinine clearance (CrCl) <60 mL/min, as estimated by the Cockcroft-Gault equation.

  7. Positive pregnancy test or lactating female participant.

  8. Positive urine drug screen, urine cotinine test, or alcohol breath test.

  9. Known allergic reactions to flunarizine or other related drugs, or to any excipient in the formulation.

  10. Clinically significant ECG abnormalities or vital signs abnormalities (systolic blood pressure lower than 90 or over 140 mmHg, diastolic blood pressure lower than 40 or over 90 mmHg, or heart rate less than 40 or over 100 bpm) at screening. Any abnormalities or deviations outside the normal range for vital signs and ECG can be repeated at the discretion of the investigator and/or designee.

  11. History of drug abuse within 1 year prior to screening or recreational use of marijuana within 1 month, or use of cocaine, phencyclidine [PCP], crack, opioid derivatives (including heroin) or amphetamine derivatives within 3 months prior to screening.

  12. History of alcohol abuse within 1 year prior to screening or regular use of alcohol within 6 months prior to screening that exceeds 14 standard drinks for females or 21 standard drinks for males of alcohol per week (1 standard drink = 375 mL of mid-strength beer 3.5% alcohol/volume, 100 mL of wine 13.5% alcohol/volume, or 30 mL of distilled alcohol 40% alcohol/volume).

  13. Use of medications within the the following timeframes prior to dosing:

    • Depot injections or drug implants: within 3 months.
    • Strong CYP2D6 inhibitors or strong CYP inducers such as fluoxetine, paroxetine, bupropion, quinidine, cinacalcet, terbinafine, mirabegron, darifenacin, rifampin, carbamazepine, phenytoin, phenobarbital, and St. John's wort: within 30 days.
    • Prescription medications: within 14 days.
    • Vaccines (including COVID 19 vaccines): within 14 days.
    • Over the counter (OTC) medications and natural health products (herbal, homeopathic, probiotics, vitamins, minerals, amino acids, essential fatty acids, protein supplements): within 7 days, except occasional paracetamol up to 2 g/day.

    No concomitant medications are permitted during the study except those required for AE management or those specifically exempted by the Investigator and/or designee as unlikely to affect PK or safety.

  14. Concomitant participation in an interventional or observational trial, or administration of an investigational device or non-biological drug within 30 days (or 5 half-lives, whichever is longer) prior to dosing, or administration of an investigational biological drug within 90 days (or 5 half-lives, whichever is longer) prior to dosing.

  15. Donation of plasma within 7 days prior to dosing or donation or loss of 500 mL or more of whole blood within 8 weeks prior to dosing.

  16. Hemoglobin <125 g/L for males and <110 g/L for females. One repeat test is permitted at the discretion of the Investigator and/or designee.

  17. Presence of orthodontic braces or orthodontic retention wires, or any physical findings in the mouth or tongue that in the opinion of the investigator and/or designee would be likely to interfere with successful completion of the dosing procedure.

  18. Any reason which, in the opinion of the Investigator and/or designee, would prevent the participant from participating in the study.

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: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Traitement A : ASP-001 Formulation A, 5 mg

ODT formulation for buccal administration

oral tablet

Autres noms:
  • Sibélium
Expérimental: Traitement B : ASP-001 Formulation A, 2 mg

ODT formulation for buccal administration

oral tablet

Autres noms:
  • Sibélium
Expérimental: Traitement C : ASP-001 Formulation B, 5 mg

ODT formulation for buccal administration

oral tablet

Autres noms:
  • Sibélium
Expérimental: Traitement D : Formulation B d'ASP-001, 2 mg

ODT formulation for buccal administration

oral tablet

Autres noms:
  • Sibélium
Comparateur actif: Treatment E: Sibelium, 5 mg

identical active ingredient

ODT formulation for buccal administration

oral tablet

Autres noms:
  • Sibélium

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Frel
Délai: Through Study Day 5 for each intervention and control

relative bioavailability calculated on the ratio of intervention to control

Through Study Day 5 for each intervention and control
AUC(0-inf)
Délai: Through Study Day 5 for each intervention and control

area under the concentration-time curve from time zero to infinity (extrapolated)

Through Study Day 5 for each intervention and control
AUC(0-t)
Délai: Through Study Day 5 for each intervention and control

area under the concentration-time curve from time zero until the last observed concentration

Through Study Day 5 for each intervention and control
Cmax
Délai: Through Study Day 5 for each intervention and control

maximal observed concentration

Through Study Day 5 for each intervention and control
Tmax
Délai: Through Study Day 5 for each intervention and control

time when the maximal concentration is observed

Through Study Day 5 for each intervention and control
T½ el
Délai: Through Study Day 5 for each intervention and control

terminal elimination half-life

Through Study Day 5 for each intervention and control
Kel
Délai: Through Study Day 5 for each intervention and control

terminal elimination rate constant

Through Study Day 5 for each intervention and control
Cl/F
Délai: Through Study Day 5 for each intervention and control

Apparent clearance

Through Study Day 5 for each intervention and control
Vz/F
Délai: Through Study Day 5 for each intervention and control

apparent volume of distribution

Through Study Day 5 for each intervention and control

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Evaluate the safety and tolerability
Délai: Throughout the study period

Measure the incidence and severity of treatment-emergent adverse events

Throughout the study period
Metabolic Profile
Délai: Through Study Day 5 for each intervention and control

Measure the plasma concentration of liver metabolites M1 (N1 dealkylation), M2 (phenyl oxidation) and M3 (N4 dealkylation)

Through Study Day 5 for each intervention and control
Dose Proportionality
Délai: Through Study Day 5 for each intervention and control

Measure plasma flunarizine concentrations of 2 mg and 5 mg for each ASP-001 ODT formulation and model for dose response

Through Study Day 5 for each intervention and control

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Peter Schrader, MBBS, FRACP, Linear Clinical Research

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)

9 avril 2026

Achèvement primaire (Réel)

23 juillet 2026

Achèvement de l'étude (Réel)

27 août 2026

Dates d'inscription aux études

Première soumission

21 février 2026

Première soumission répondant aux critères de contrôle qualité

25 février 2026

Première publication (Réel)

3 mars 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

6 octobre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

2 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • ASP-001-01

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

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .