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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)

2026年6月9日 更新者: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.

調査の概要

研究の種類

介入

入学 (推定)

120

段階

  • フェーズ2
  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
プラセボコンパレーター:対照群
プラセボ
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.
実験的: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.
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change from baseline in ADAS-Cog13 score at Month 6
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Change from baseline in ADAS-Cog13 score at Month 12 (OLE)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)

その他の成果指標

結果測定
メジャーの説明
時間枠
Rate of ≥90% medication adherence at Month 6
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠:Baseline, Month 6, Month 12 (OLE)
Change from baseline in gut microbiota metabolite-related indicators.
Baseline, Month 6, Month 12 (OLE)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2027年5月1日

研究の完了 (推定)

2027年12月1日

試験登録日

最初に提出

2026年5月11日

QC基準を満たした最初の提出物

2026年5月11日

最初の投稿 (実際)

2026年5月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月11日

QC基準を満たした最後の更新が送信されました

2026年6月9日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • KY2026-015

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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