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Short Term Efficacy and Safety of Perispinal Administration of Etanercept in Mild to Moderate Alzheimer's Disease

Information source: Life Extension Foundation Inc.
Information obtained from ClinicalTrials.gov on February 07, 2013
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Alzheimer's Disease

Intervention: Etanercept (Biological); Curcum.Luteol.Theaflav.Lip.Acid,FishOil,Quercet.,Resveratr. (Dietary Supplement)

Phase: Phase 1

Status: Recruiting

Sponsored by: Life Extension Foundation Inc.

Official(s) and/or principal investigator(s):
Paul H. Wand, M.D., Principal Investigator, Affiliation: Paul H. Wand M.D., P.A.

Overall contact:
Dr. Steven Hirsh, Phone: 954-202-7660, Ext: 7679, Email: shirsh@lef.org

Summary

While the cause of AD is still unknown, evidence suggests it develops because of a complex series of events in the brain that occur over time. Two pathways possibly involved in development of AD are inflammation and oxidative stress. Scientists have linked chronic inflammatory events in the brain with the onset and progression of Alzheimer's Disease. Oxidative stress has also been implicated in the pathogenesis of a number of neurological disorders including Alzheimer's Disease.

Etanercept (Enbrel®) is an approved drug for the treatment of several forms of arthritis when administered by injection. Some research suggests that etanercept, when administered by injection into the tissues close to the spinal column (perispinally), may modulate certain aspects of the immune system and provide some beneficial effect for people with Alzheimer's disease. Studies suggest that supplementation with specific nutrients may also have a positive effect in support of cognitive function.

This study will be conducted at one research office with volunteers who have been diagnosed with mild to moderate Alzheimer's disease. Each qualifying participant will be randomly assigned to receive an etanercept injection plus nutritional supplements for 6 weeks followed by a crossover and a washout period of 4 weeks to then receiving nutritional supplements alone or vice versa for another 6 weeks.

Participants will undergo blood and urine safety assessments at the beginning and end of each 6 week treatment period. During 4 of the 6 weekly visits in the treatment period with the injections, you will complete the cognitive tests twice; once before and once 2 hours after the injection. During 4 of the 6 weekly visits in the treatment period without the injections, you will also complete the cognitive tests twice; once before and once 2 hours after being asked to lie down onto a table for 5 minutes. You will be allowed to continue your standard of care for Alzheimer's disease throughout your participation in the study.

Clinical Details

Official title: Open Label,Crossover,Pilot Study to Assess the Efficacy & Safety of Perispinal Admin.of Etanercept(Enbrel®) in Comb.w/Nutritional Supplements vs. Nutritional Supplements Alone in Subj. w/Mild to Mod. Alzheimer's Disease Receiving Std. Care.

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Primary outcome: Difference in effects of treatment for 6 weeks with etanercept + nutritional supplements versus nutritional supplements alone on the Mini-Mental Status Examination (MMSE) score.

Secondary outcome:

Difference in the effects of treatment for 6 weeks with etanercept + nutritional supplements versus nutritional supplements alone on the Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-cog) score.

Difference in the effects of treatment for 6 weeks with etanercept + nutritional supplements versus nutritional supplements alone on the Montreal Cognitive Assessment (MoCA) score.

Eligibility

Minimum age: 60 Years. Maximum age: 85 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Subject is aged 60-85 years

- Subject has a diagnosis of Alzheimer's disease according to the NINCDS- ADRDA

criteria (National Institute of Neurological and Communicative Disorders and Stroke NINCDS] and Alzheimer's Disease and Related Disorders Association [ADRDA]).

- Subject is not institutionalized (for example, lives independently, lives

independently in a residential home for the elderly, or is a day patient at a care center)

- Subject has a Hachinski Ischemia Score of ≤ 4.

- Subject has a total MoCA score of < 26 at screening.

- Subject has an MMSE score of 11 to 24 at screening.

- Subject has an ADAS-cog score of 12 to 25 at screening.

- Subject has experienced a gradual and progressive cognitive decline in the 6 months

before the screening visit.

- Subject provides informed consent to participate in the study or has a legally

acceptable representative who provides consent.

- Subject has a responsible caregiver who consents to supporting the subject in his/her

study participation (for example, by accompanying the subject on each study visit).

- Subject is surgically sterile, agrees to use an acceptable method of birth control as

defined in section 5. 4 or, for females, is post- menopausal.

- Subject agrees to stop taking any vitamin, mineral, or dietary supplements he/she is

currently taking that have any components of the nutritional supplements utilized in the study at least 7 days before randomization (Visit 2) and agrees to not use any new vitamin, mineral, or dietary supplement product other than those provided by the investigator until after the subject is discharged from the study.

Exclusion Criteria:

- A neurologic disorder, such as seizures, multiple sclerosis, neurodegenerative

disorders (eg, Parkinson's disease), or dementia other than Alzheimer's type (including that caused by small strokes or cerebrovascular disease)

- Cognitive impairment from any condition other than Alzheimer's disease, such as that

resulting from acute cerebral trauma, cerebral damage due to a lack of oxygen, infections such as meningitis or AIDS, significant endocrine or metabolic disease, mental retardation, or a brain tumor

- Cardiovascular or cerebrovascular disease, such as congestive heart failure,

uncontrolled hypertension (BP ≥ 140/90 mmHg at screening), and a history of stroke

- Renal impairment/disease, defined as serum creatinine > 1. 5 mg/dL

- Hepatic impairment, defined as Alanine Aminotransferase (ALT) or Aspartate

Aminotransferase (AST) > 3 times the upper limit of normal OR has a history of a positive blood screen for hepatitis B surface antigen or hepatitis C antibody.

- Type I or II diabetes mellitus

- Significant or uncontrolled psychiatric disease

- Gastrointestinal disease, such as active peptic ulcer, gallstones, gallbladder

disease, or biliary tract obstruction, or a history of cholecystectomy

- Hematologic disorders

- Pulmonary or lung disorders

- Immune system disorder, such as HIV/AIDS

- History of cancer within 10 years before screening (except localized skin cancer

without metastases or in situ cervical cancer)

- History of chronic or recurrent infection (including tuberculosis) OR, in the 7 days

before Visit 2 (randomization), any known infection or body temperature > 38. 6Âş C (101. 5Âş F)

- Subject is pregnant or breastfeeding at screening.

- Subject has intolerance or allergy to Enbrel®, latex, or any of Enbrel's components.

- Subject is currently consuming more than 6 standard alcoholic beverages a week. A

standard alcoholic beverage is defined as 12 ounces of beer, 5 ounces of wine, or 1. 5 ounces of liquor.

- Subject is currently taking and unable or unwilling to stop taking anticoagulant or

antiplatelet herbs and supplements such as angelica, clove, danshen, garlic, ginger, ginkgo, Panax ginseng, red clover, or willow for at least 7 days before the randomization visit (Visit 2) and throughout the study.

- Subject is currently taking and unable or unwilling to stop taking any of the

prohibited medications in protocol section 5. 3.2 for at least 7 days before the randomization visit (Visit 2) and throughout the study.

- Subject had major surgery within the 4 weeks before screening.

- Subject has any condition or abnormality that, in the opinion of the investigator,

would compromise the safety of the subject or the quality of the study data.

- Subject is participating or has participated in another research study within 30 days

before the screening visit

- Subject or subject's caregiver is unable or unwilling to comply with the study

procedures.

Locations and Contacts

Dr. Steven Hirsh, Phone: 954-202-7660, Ext: 7679, Email: shirsh@lef.org

Paul H. Wand M.D., P.A., Coral Springs, Florida 33065, United States; Recruiting
Cherryl, Phone: 954-344-9772
Paul H. Wand, M.D., Principal Investigator
Additional Information

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Starting date: February 2010
Last updated: October 25, 2012

Page last updated: February 07, 2013

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