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A Study of the Metabolic Reconstruction Oral Biologics (Gut-X-001) Medication in People With Alzheimer's Disease (ESCAPE-AD) (ESCAPE-AD)

9 de junho de 2026 atualizado por: yilong Wang, Beijing Tiantan Hospital

Efficacy, Safety, and Feasibility of Metabolic ReConstruction Oral Biologics (Gut-X-001) in Patients With Alzheimer's Disease: An Exploratory Clinical Trial (ESCAPE-AD)

This is an exploratory clinical trial aimed at preliminarily evaluating the efficacy, safety, and feasibility of orally administered Gut-X-001 in patients with Alzheimer's disease (AD). An open-label extension (OLE) study will also be conducted to further investigate the effects of Gut-X-001. The study will assess the effects of Gut-X-001 on cognitive function, activities of daily living, neuroimaging indicators, and AD-related plasma biomarkers in AD patients. Safety will be systematically monitored, including the incidence of adverse events and changes in hematological and organ function parameters. Furthermore, the study will explore the regulatory effects of Gut-X-001 versus placebo on venous blood redox-related indicators and gut microbiota metabolite levels at different time points, providing a basis for multi-target intervention strategies and offering systematic evidence for the scientific rationale, feasibility, and safety of Gut-X-001 in the clinical management of AD.

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Tipo de estudo

Intervencional

Inscrição (Estimado)

120

Estágio

  • Fase 2
  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria

  1. Age ≥50 and ≤85 years.
  2. Diagnosis of Alzheimer's disease confirmed by a qualified neurologist based on the 2024 National Institute on Aging - Alzheimer's Association (NIA-AA) diagnostic criteria, with at least one abnormal core biomarker, including amyloid PET, CSF Aβ42/40, phosphorylated tau181 (p-tau181)/Aβ42, total tau (t-tau)/Aβ42, or plasma p-tau217.
  3. MMSE score meeting the following criteria:

    If years of education ≤6: MMSE score between 16 and 24 (inclusive); If years of education >6: MMSE score between 18 and 27 (inclusive).

  4. Clinical Dementia Rating (CDR) global score of 0.5 (for MCI due to AD) or 1.0 (for mild AD dementia).
  5. If receiving acetylcholinesterase inhibitor (AChEI) and/or memantine therapy, the dose must have been stable for at least 3 months prior to screening.
  6. Participants must have a reliable caregiver who has frequent contact with the participant (at least 4 days per week and at least 2 hours per day). The caregiver must accompany the participant to all study visits, provide meaningful input for scale assessments through sufficient interaction with the participant, and remain consistent throughout the study period wherever possible.
  7. The participant or their legally authorized representative is able and willing to provide written informed consent.

Exclusion Criteria

  1. Presence of other conditions that may contribute to cognitive impairment, including neurological disorders (e.g., vascular cognitive impairment, Parkinson's disease, frontotemporal dementia, Lewy body dementia) or psychiatric and affective disorders (e.g., severe anxiety/depression, schizophrenia).
  2. Diagnosis of acute cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage, myocardial infarction, or heart failure within the 3 months prior to screening.
  3. Presence of other active or significant neurological conditions, including recurrent epileptic seizures, intracranial space-occupying tumors, vascular malformations (including arteriovenous malformations, arterial malformations, or cavernous malformations), or untreated aneurysms with a diameter >3 mm.
  4. Severe hepatic impairment [ALT or AST >3× upper limit of normal (ULN), or concurrent acute hepatitis, chronic active hepatitis, or liver cirrhosis], renal impairment [estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m²], active malignancy, severe anemia, chronic obstructive pulmonary disease (COPD), immune system disorders, uncontrolled diabetes, or uncontrolled hypertension [systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg].
  5. Currently receiving medications that may interfere with study outcomes.
  6. Known hypersensitivity to the investigational drug or any of its excipients.
  7. Formal education of 1 year or less.
  8. Known history of severe organic disease or an anticipated survival of less than 12 months.
  9. Pregnant or breastfeeding women, or women of childbearing potential who refuse to use contraceptive measures.
  10. Participation in another clinical study within 30 days prior to screening, or currently enrolled in another clinical study.
  11. Any other condition that, in the investigator's judgment, makes the participant unsuitable for enrollment or unable to complete the study procedures and follow-up visits, such as psychiatric illness or physical conditions that preclude compliance with study requirements.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Quadruplicar

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de Placebo: Grupo de controle
Placebo
Participants will receive 4 placebo capsules (0 mg of active ingredient per capsule) orally per administration, 3 times daily (at 8:00 AM, 12:00 PM, and 10:00 PM), administered before meals and before bedtime. Placebo capsules are identical in appearance to the active Gut-X-001 capsules to maintain blinding.
Experimental: Low-Dose Group
Low-Dose Gut-X-001
Participants will receive Gut-X-001 orally at a dose of 2 active capsules (10 mg of active ingredient per capsule) plus 2 placebo capsules (0 mg of active ingredient per capsule) per administration, 3 times daily (at 8:00 AM, 12:00 PM, and 10:00 PM), administered before meals and before bedtime. Total active ingredient per administration: 20 mg; total daily dose: 60 mg.
Experimental: High-Dose Group
High-Dose Gut-X-001
Participants will receive Gut-X-001 orally at a dose of 4 active capsules (10 mg of active ingredient per capsule) per administration, 3 times daily (at 8:00 AM, 12:00 PM, and 10:00 PM), administered before meals and before bedtime. Total active ingredient per administration: 40 mg; total daily dose: 120 mg.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in ADAS-Cog13 score at Month 6
Prazo: Baseline, Month 6
Change from baseline in the Alzheimer's Disease Assessment Scale - Cognitive Subscale 13-item version (ADAS-Cog13) score. Higher scores indicate greater cognitive impairment.
Baseline, Month 6

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in ADAS-Cog13 score at Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline and from Month 6 in ADAS-Cog13 score during the open-label extension (OLE) phase. Higher scores indicate greater cognitive impairment.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in ADCS-ADL score at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in the Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL) scale score. Lower scores indicate greater functional impairment.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in PSQI score at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in the Pittsburgh Sleep Quality Index (PSQI) score. Higher scores indicate poorer sleep quality.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in NPI score at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in the Neuropsychiatric Inventory (NPI) score. Higher scores indicate more severe neuropsychiatric symptoms.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in brain volume and hippocampal volume at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in brain volume and hippocampal volume as measured by structural neuroimaging (MRI).
Baseline, Month 6, Month 12 (OLE)
Change from baseline in SCD-Q9 score at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in the Subjective Cognitive Decline Questionnaire 9-item version (SCD-Q9) score.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in CDR-SB score at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in the Clinical Dementia Rating - Sum of Boxes (CDR-SB) score. Higher scores indicate greater disease severity.
Baseline, Month 6, Month 12 (OLE)

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Rate of ≥90% medication adherence at Month 6
Prazo: Month 6
Proportion of participants who complete at least 90% of the prescribed dosing regimen during the double-blind phase.
Month 6
Incidence of clinically significant abnormal CBC findings at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants meeting any of the following criteria: (i) anemia (hemoglobin <90 g/L in males or <85 g/L in females, or requiring transfusion); (ii) thrombocytopenia (platelets <50.0×10⁹/L or requiring transfusion); (iii) leukopenia (WBC <1.5×10⁹/L, lymphocytes <0.5×10⁹/L, or neutrophils <0.60×10⁹/L); or (iv) any CBC abnormality deemed clinically significant by the investigator.
Day 7, Month 3, Month 6, Month 12 (OLE)
Incidence of clinically significant hepatic biochemical abnormalities at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants meeting any of the following criteria: (i) ALT or AST >5× ULN; (ii) ALT or AST >3× ULN with total bilirubin >2× ULN (Hy's Law); or (iii) ALT or AST >3× ULN with symptoms of hepatic injury (e.g., nausea, vomiting, jaundice).
Day 7, Month 3, Month 6, Month 12 (OLE)
Incidence of acute kidney injury or significant renal function deterioration at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants meeting any of the following criteria: (i) acute: serum creatinine increase ≥1.5-fold from baseline (confirmed or presumed to have occurred within 7 days) or increase ≥26.5 µmol/L (0.3 mg/dL) within 48 hours; or (ii) chronic: eGFR decrease ≥30% from baseline.
Day 7, Month 3, Month 6, Month 12 (OLE)
Incidence of body weight increase >10% from baseline at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants with a body weight increase of more than 10% compared to baseline.
Day 7, Month 3, Month 6, Month 12 (OLE)
Incidence of binge eating episodes at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants experiencing binge eating, defined as eating an unusually large amount of food within a discrete period (e.g., 2 hours) accompanied by a sense of loss of control over eating behavior.
Day 7, Month 3, Month 6, Month 12 (OLE)
Incidence of adverse events and serious adverse events at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants experiencing any adverse event (AE) or serious adverse event (SAE) during the study period.
Day 7, Month 3, Month 6, Month 12 (OLE)
Incidence of drug-related adverse events and serious adverse events at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants experiencing AEs or SAEs assessed by the investigator as related to the study drug.
Day 7, Month 3, Month 6, Month 12 (OLE)
Rate of treatment discontinuation due to adverse events or serious adverse events at Day 7, Month 3, Month 6, and Month 12 (OLE)
Prazo: Day 7, Month 3, Month 6, Month 12 (OLE)
Proportion of participants who discontinue study treatment due to AEs or SAEs.
Day 7, Month 3, Month 6, Month 12 (OLE)
Change from baseline in venous blood H₂O₂ concentration and oxidative stress-related indicators at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in venous blood hydrogen peroxide (H₂O₂) concentration and other oxidative stress-related indicators.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in Aβ and tau protein deposition assessed by PET-CT at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in amyloid-β (Aβ) and tau protein deposition as assessed by PET-CT imaging.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in AD-related plasma biomarker levels at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in plasma biomarker levels including p-Tau217, NfL, NELL1, ENO2, ST2, LIFR, CD33, CHI3L1, PPY, FAM3B, and other relevant markers.
Baseline, Month 6, Month 12 (OLE)
Change from baseline in gut microbiota metabolite levels at Month 6 and Month 12 (OLE)
Prazo: Baseline, Month 6, Month 12 (OLE)
Change from baseline in gut microbiota metabolite-related indicators.
Baseline, Month 6, Month 12 (OLE)

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de agosto de 2026

Conclusão Primária (Estimado)

1 de maio de 2027

Conclusão do estudo (Estimado)

1 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

11 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

11 de maio de 2026

Primeira postagem (Real)

18 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

11 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

9 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • KY2026-015

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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