- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01255163
A Pilot Clinical Trial of Exendin-4 in Alzheimer's Disease
A Pilot Study of Exendin-4 in Alzheimer s Disease
Background:
Exendin-4 (or Exenatide) is a medication currently used to treat diabetes that has shown promising results in animal and cellular models of Alzheimer's disease. It is possible that Exendin-4 may be a treatment for Alzheimer's disease, which involves the gradual deterioration and death of neurons. Researchers are interested in studying the safety and comparing the effects of Exendin-4 with placebo on cognitive performance, clinical progression of dementia, various chemicals measured in blood and cerebrospinal fluid, and brain MRI, in individuals with early-stage Alzheimer's disease or mild cognitive impairment.
Objectives:
To determine the safety and tolerability of twice daily administration of Exendin-4, as well as to acquire preliminary evidence for effects on cognitive performance, clinical progression of dementia, various chemicals measured in blood and cerebrospinal fluid, and brain MRI, in individuals with early-stage Alzheimer's disease or mild cognitive impairment.
Eligibility:
Individuals at least 60 years of age who have objective evidence of early-stage Alzheimer's disease or mild cognitive impairment in screening testing.
Design:
- Participants will be screened.
- Following the telephone screening, two in-person screening visits to determine eligibility.
- The screening visit will involve a medical history and neurological examination, tests of memory and cognition, a lumbar puncture, collection of blood and saliva samples, and brain Magnetic Resonance Imagine (MRI) studies. Participants will be required to appoint a Durable Power of Attorney for research and medical care during this protocol.
- Eligible participants will be divided into two groups (double-blind randomization). One group will receive Exendin-4 SC twice daily, and the other will receive a placebo. Participants will keep a medication diary and will be scheduled for additional study visits 1 and 2 weeks after the start of the treatment.
- Participants will have regular followup visits with blood tests, cognitive tests, imaging studies, and other examinations 6, 12, and 18 months after the start of the treatment. Another lumbar puncture may be performed optionally at the 18-month followup visit.
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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Maryland
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Baltimore, Maryland, Stati Uniti, 21224
- National Institute on Aging, Clinical Research Unit
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
- INCLUSION CRITERIA:
- Age > 60
- Clinical Dementia Rating (global CDR) of 0.5 or 1. Memory box score must be at least 0.5.
- Mini Mental Status Exam (MMSE) > 20
- Clinical diagnosis of (amnestic or mixed) MCI or early AD and Memory deficit on neuropsychological or clinical testing.
- Hamilton Depression Scale score of less than or equal to 12 on the 17-item scale
- CSF A beta 42 < 192 (+- 10%) pg/ml (given an intra-subject laboratory variability ~ 10%)
Medications stable for at least 4 weeks prior to screening. In particular:
- Participants may take stable doses of antidepressants, chronic anxiolytics or sedative hypnotics, if started at least 4 weeks or longer prior to screening
- Cholinesterase inhibitors and/or memantine are allowable, if started at least 4 weeks prior to screening
- Participants will not be asked to discontinue medications without permission from their primary care provider (PCP) or specialist.
- Fluency in English
- At the time of enrollment, participants must have the ability to provide informed consent and make health care decisions.
- An informant or caregiver who has frequent contact with the participant (e.g. an average of 10 hours per week or more) must be appointed to serve as Durable Power of Attorney (DPA) for research and medical care at NIA, accompany the participant to clinic visits and provide historical information regarding the participant s cognitive status, and assist participants with/administer injections of the investigational medication.
- Good general health with no additional disease states that could interfere with the study.
EXCLUSION CRITERIA:
- Other significant neurological disease of the Central Nervous System (such as Parkinson s disease, atypical Parkinsons disease, Multi-infarct Dementia, Frontotemporal Dementia, Huntington s disease, Normal Pressure Hydrocephalus, brain tumor, Progressive Supranuclear Palsy, Epilepsy, Subdural Hematoma or Multiple Sclerosis)
- A history of significant head trauma followed by persistent neurologic defaults or known structural brain abnormalities
- Positive RPR or HIV
- Abnormal PT/PTT and INR (1.5 standard deviation over the upper normal limit) increasing the risk for LP related bleeding/hematoma; platelet count <100,000/microliters.
- Anti-coagulant therapy (such as coumadin). Aspirin up to 325 is allowed.
- Investigators unable to obtain CSF, failure of Lumbar Puncture after a limited number of unsuccessful attempts).
- History of psychiatric disease with significant impairment in thought processes (e.g. schizophrenia, bipolar disease, psychosis). Participants who develop psychiatric conditions necessitating treatment after their enrollment will not be dropped from the study. The high incidence of late-onset depression and anxiety among individuals with MCI and AD requires that participants with depression, and/or anxiety should not be excluded from the cohort to maintain the ecological validity of the results.
- Current abuse of alcoholic beverages (> 7 in women and >14 in men) or substance abuse.
- Known diagnosis of diabetes at the time of enrollment or new diagnosis of diabetes based on the findings of elevated fasting blood glucose (= or >126 mg/dl) and/or the oral glucose tolerance test at screening (>200 mg/dl at two hours).
- Severe renal impairment (creatinine clearance <30 ml/min) or end-stage renal disease. Individuals with moderate renal impairment (creatinine clearance 30 to 50 ml/min) may be enrolled in the study, but their BUN and Creatinine will be monitored during each visit after drug initiation and extra safety visits will be conducted at 3, 9, and 15 months.
- Current or previous treatment with Exendin-4 (Exenatide, trade name Byetta.)
- History of pancreatitis, active upper GI, hepatic or gallbladder disease
- Personal or family history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia syndrome type 2
- History of repeated hypoglycemia
- Body mass index (BMI) < 18 on enrollment (given the expected weight loss caused by Exendin-4 and dementia). In the BLSA, participants with age > 65 had a mean BMI of 25.8 with SD of 3.9 Exendin-4 has been shown to cause an average 5.3 kg weight loss, with 95% CI: 6 to 4.5 kg (126).
- Allergy to Exendin-4 or to substances in the injection pen (metacresol, mannitol, glacial acetic acid, sodium acetate trihydrate, water for injection).
- Participation in other studies of investigational treatments for Alzheimer s disease in the last year.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Exendin-4
Exenatide 5 mcg or 10 mcg SC twice daily
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Exenatide 5 mcg or 10 mcg SC twice daily
Altri nomi:
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Comparatore placebo: Placebo
Placebo SC twice daily
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Placebo SC twice daily
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Number of Participants With Incidence of Nausea
Lasso di tempo: 18 months
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Tolerability of exenatide (nausea is the most common expected adverse event of exenatide)
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18 months
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Mini Mental State Examination (MMSE)
Lasso di tempo: 18 months
|
Scale range: 0 - 30 points (higher is better)
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18 months
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Alzheimer's Disease Assessment Scale-cognitive Subscale (ADAS-cog70)
Lasso di tempo: 18 months
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Alzheimer's dementia scale cognitive sub-scale range: 0 - 70 points (higher is worse)
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18 months
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Clinical Dementia Rating (CDR) Global Score
Lasso di tempo: 18 months
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Clinical Dementia Rating global score range: 0 (no dementia); 0.5 (Mild Cognitive Impairment); 1 (mild dementia); 2 (moderate dementia); 3 (severe dementia).
Higher is worse.
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18 months
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Clinical Dementia Rating (CDR) Sum of Boxes
Lasso di tempo: 18 months
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Sum of the Clinical Dementia Rating "boxes" (memory, orientation, judgment and problem solving, community affairs, home and hobbies, personal care).
Each box is rated as 0, 0.5, 1, 2 or 3. Range for the sum of boxes is 0 - 18. Higher scores reflect a greater severity of dementia.
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18 months
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Cerebrospinal Fluid (CSF) Total Tau
Lasso di tempo: 18 months
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Total Tau measured in CSF using Luminex xMAP technology and INNO-BIA Alz Bio3 kits (Research Use Only) provided by Fujirebio
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18 months
|
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Cerebrospinal Fluid phospho181-tau (CSF p181-tau)
Lasso di tempo: 18 months
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p-181-Tau measured in CSF using Luminex xMAP technology and INNO-BIA Alz Bio3 kits (Research Use Only) provided by Fujirebio
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18 months
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Cerebrospinal Fluid Amyloid-beta 42 (CSF Abeta42)
Lasso di tempo: 18 months
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Abeta42 peptide measured in CSF using Luminex xMAP technology and INNO-BIA Alz Bio3 kits (Research Use Only) provided by Fujirebio
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18 months
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Body Mass Index (BMI)
Lasso di tempo: 18 months
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Body Mass Index defined as a person's weight in kilograms (kg) divided by his or her height in meters squared.
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18 months
|
Collaboratori e investigatori
Pubblicazioni e link utili
Pubblicazioni generali
- Kapogiannis D, Mattson MP. Disrupted energy metabolism and neuronal circuit dysfunction in cognitive impairment and Alzheimer's disease. Lancet Neurol. 2011 Feb;10(2):187-98. doi: 10.1016/S1474-4422(10)70277-5. Epub 2010 Dec 10. Erratum In: Lancet Neurol. 2011 Feb;10(2):115.
- Bomfim TR, Forny-Germano L, Sathler LB, Brito-Moreira J, Houzel JC, Decker H, Silverman MA, Kazi H, Melo HM, McClean PL, Holscher C, Arnold SE, Talbot K, Klein WL, Munoz DP, Ferreira ST, De Felice FG. An anti-diabetes agent protects the mouse brain from defective insulin signaling caused by Alzheimer's disease- associated Abeta oligomers. J Clin Invest. 2012 Apr;122(4):1339-53. doi: 10.1172/JCI57256.
- Mullins RJ, Mustapic M, Chia CW, Carlson O, Gulyani S, Tran J, Li Y, Mattson MP, Resnick S, Egan JM, Greig NH, Kapogiannis D. A Pilot Study of Exenatide Actions in Alzheimer's Disease. Curr Alzheimer Res. 2019;16(8):741-752. doi: 10.2174/1567205016666190913155950.
- Muscogiuri G, DeFronzo RA, Gastaldelli A, Holst JJ. Glucagon-like Peptide-1 and the Central/Peripheral Nervous System: Crosstalk in Diabetes. Trends Endocrinol Metab. 2017 Feb;28(2):88-103. doi: 10.1016/j.tem.2016.10.001. Epub 2016 Oct 27.
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Disordini mentali
- Malattie del cervello
- Malattie del sistema nervoso centrale
- Malattie del sistema nervoso
- Disturbi neurocognitivi
- Malattie Neurodegenerative
- Demenza
- Tauopatie
- Disturbi cognitivi
- Malattia di Alzheimer
- Disfunzione cognitiva
- Agenti ipoglicemizzanti
- Effetti fisiologici delle droghe
- Ormoni
- Ormoni, sostituti ormonali e antagonisti ormonali
- Agenti anti-obesità
- Incretine
- Exenatide
Altri numeri di identificazione dello studio
- 100423
- 10-AG-0423
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
prodotto fabbricato ed esportato dagli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Exendin-4 SC
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Carl T. Hayden VA Medical CenterAmerican Diabetes Association; Amylin Pharmaceuticals, LLC.CompletatoDiabete mellito di tipo 2Stati Uniti
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University Hospital, Basel, SwitzerlandUniversity Hospital Inselspital, Berne; Desirée and Niels Yde's Foundation, Zürich...CompletatoIpoglicemia iperinsulinemica endogenaSvizzera
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Peking Union Medical College HospitalAttivo, non reclutante
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CSPC ZhongQi Pharmaceutical Technology Co., Ltd.Completato
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Zealand University HospitalUniversity of Copenhagen; Glostrup University Hospital, CopenhagenSconosciuto
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Radboud University Medical CenterUniversity of CoimbraSconosciutoDiabete mellito, tipo 2 | Diabete mellitoOlanda
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Peking Union Medical College HospitalNational Institute for Biomedical Imaging and Bioengineering (NIBIB)Sconosciuto68Ga-NOTA-exendin-4 PET/TC per la localizzazione dell'insulinoma e la diagnosi della nesidioblastosiInsulinoma | NesidioblastosiCina
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The University of Texas Health Science Center at...ReclutamentoChirurgia Post-bariatricaStati Uniti
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AstraZenecaUniversity of PittsburghCompletatoSARS-CoV-2, COVID-19Stati Uniti
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Amylyx Pharmaceuticals Inc.A disposizioneIpoglicemia post-bariatricaStati Uniti