- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07804381
Disease-modifying Efficacy of Sitagliptin Therapy in Early-stage Parkinson's Disease (ARREST-PD)
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 2 Trial Evaluating the Disease-modifying Efficacy of Sitagliptin Therapy in Early-stage Parkinson's Disease
Parkinson's disease (PD) is a progressive neurodegenerative disorder pathologically characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta and the accumulation of α-synuclein (α-syn) aggregates. To date, all approved treatments, including levodopa, are primarily limited to symptomatic relief, and no disease-modifying therapy (DMT) has been established to fundamentally slow or halt disease progression.
Large-scale epidemiological cohort studies conducted in Taiwan, Sweden, the United Kingdom, and other countries have consistently reported that, among patients with diabetes, DPP-4 inhibitor users had an approximately 30%-40% lower risk of developing Parkinson's disease compared with non-users.
This study aims to evaluate whether 72 weeks of treatment with sitagliptin (100 mg once daily), compared with placebo, delays the time to confirmed motor progression in patients with early-stage PD receiving stable levodopa monotherapy. Confirmed motor progression is defined as an increase of ≥5 points from baseline in the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III score assessed in the OFF state.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Philhyu Lee, Professor
- Numéro de téléphone: +82-2-2228-1608
- E-mail: PHLEE@yuhs.ac
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Male or female participants aged 50 to 80 years, inclusive.
- Participants diagnosed with Clinically Established Parkinson's Disease or Clinically Probable Parkinson's Disease according to the Movement Disorder Society (MDS) Clinical Diagnostic Criteria for Parkinson's Disease (Postuma et al., 2015).
- Participants diagnosed with Parkinson's disease within 3 years prior to screening.
- Participants who are either treatment-naïve to antiparkinsonian medications at screening or receiving stable levodopa monotherapy, defined as maintenance of the same levodopa dose for at least 12 weeks immediately prior to screening without concomitant use of other antiparkinsonian medications.
- Hoehn and Yahr stage 1 or 2 in the ON state.
- Participants with documented evidence, based on ¹⁸F-FP-CIT PET performed at the investigational site within 36 months prior to screening, of reduced dopamine transporter (DAT) availability in the posterior putamen. Raw DICOM files must be retrievable and suitable for quantitative analysis of standardized uptake value ratio (SUVR) or specific binding ratio (SBR) by the central reader. Participants without an available prior ¹⁸F-FP-CIT PET result must agree to undergo an additional ¹⁸F-FP-CIT PET scan.
- Participants with documented brain MRI performed at any time prior to screening or during the screening period, confirming exclusion of causes other than Parkinson's disease, including atypical parkinsonian syndromes such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP), cerebrovascular disease, normal-pressure hydrocephalus, and brain tumor. The T1-weighted sequence must be suitable for comparison with the follow-up MRI performed at Visit 9.
- Mini-Mental State Examination (MMSE) score ≥24, to exclude severe cognitive impairment.
- Participants who understand the clinical trial protocol and voluntarily provide written informed consent.
- Participants who are able and willing to comply with follow-up visits and study assessments throughout the entire study period.
Exclusion Criteria:
- Participants with suspected atypical parkinsonian syndromes, including progressive supranuclear palsy (PSP), multiple system atrophy (MSA), corticobasal syndrome (CBS), or other atypical parkinsonian disorders.
- Participants with vascular parkinsonism, drug-induced parkinsonism, or toxin-induced parkinsonism.
- Participants with secondary parkinsonism due to causes such as normal-pressure hydrocephalus, brain tumor, or other identifiable secondary causes.
- Participants currently receiving dopaminergic medications other than levodopa, including dopamine agonists, monoamine oxidase-B (MAO-B) inhibitors, catechol-O-methyltransferase (COMT) inhibitors, amantadine, or other antiparkinsonian medications.
- Participants with levodopa-induced motor fluctuations or levodopa-induced dyskinesia (LID) that interfere with activities of daily living, defined as a score of ≥2 on MDS-UPDRS Part IV Item 4.1 or 4.2.
- History of hypersensitivity to sitagliptin or any other dipeptidyl peptidase-4 (DPP-4) inhibitor.
- Current treatment with a DPP-4 inhibitor or glucagon-like peptide-1 (GLP-1) receptor agonist.
- History of acute or chronic pancreatitis.
- Acute cholecystitis or cholangitis.
- Participants with previously diagnosed diabetes mellitus who are currently receiving antidiabetic medication.However, participants with a diagnosis of diabetes mellitus who are not currently receiving antidiabetic medication, or those found to have HbA1c ≥6.5% during screening, may be enrolled. Participants with HbA1c ≥7.5% will be excluded because combination antidiabetic therapy may be required.
- Estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m², indicating moderate or greater renal impairment.
- Hepatic dysfunction, defined as AST or ALT >3 times the upper limit of normal (ULN).
- Pancreatic enzyme abnormality, defined as amylase or lipase >3 times the ULN.
- Clinically significant cardiovascular disease, including New York Heart Association (NYHA) Class III-IV heart failure, myocardial infarction, or stroke within 6 months prior to screening.
- History of malignancy within 5 years prior to screening, except for completely treated non-melanoma skin cancer.
- Uncontrolled, clinically significant psychiatric disorder.
- Participants who are pregnant or breastfeeding, or women of childbearing potential who are unwilling or unable to use an appropriate method of contraception.
- Participation in another clinical trial within 30 days prior to screening.
- Participants considered unsuitable for participation in the clinical trial based on the investigator's clinical judgment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Sitagliptin
Sitagliptin 100 mg, one tablet orally once daily, with or without food, for 72 weeks.
|
Sitagliptin 100 mg, one tablet orally once daily, with or without food, for 72 weeks.
|
|
Comparateur placebo: Sitagliptin placebo
One placebo tablet orally once daily, with or without food, for 72 weeks.
(The placebo will be manufactured to be indistinguishable from the investigational product in terms of appearance, color, size, and weight in order to maintain blinding.)
|
One placebo tablet orally once daily, with or without food, for 72 weeks.
(The placebo will be manufactured to be indistinguishable from the investigational product in terms of appearance, color, size, and weight in order to maintain blinding.)
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Time to Confirmed Motor Progression (TTE)
Délai: From randomization every 12 weeks through Week 76.
|
Time from randomization (V2) to the first observed increase of ≥5 points from baseline in the MDS-UPDRS Part III score, confirmed at the next scheduled visit (approximately 12 weeks later), assessed in the OFF state in the morning prior to levodopa administration and after ≥12 hours since the last levodopa dose.
|
From randomization every 12 weeks through Week 76.
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Synucleinopathies
- Maladies du cerveau
- Maladies du système nerveux central
- Maladies du système nerveux
- Maladies neurodégénératives
- Troubles du mouvement
- Troubles parkinsoniens
- Maladies des noyaux gris centraux
- Maladie de Parkinson
- Composés hétérocycliques, 1 anneau
- Composés hétérocycliques
- Azoles
- Pyrazines
- Triazoles
- Phosphate de sitagliptine
Autres numéros d'identification d'étude
- 4-2026-0566
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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 .