Safety and Tolerability of Etanercept in Alzheimer's Disease

Alzheimer's Disease Clinical Trial

— STEADI-09  

Official title:

A Phase 2, Double-blind, Placebo-controlled Study of the Safety and Tolerability of Etanercept in Patients With Alzheimer's Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01068353
• Other study ID #: STEADI-09
• Secondary ID: 2009-013400-31
• Status: Completed
• Phase: Phase 2
• First received: February 10, 2010
• Last updated: April 22, 2014
• Start date: January 2011

Study information

• Verified date: April 2014
• Source: University of Southampton
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

The primary aim of the study is to determine the safety and tolerability of etanercept in subjects with Alzheimer's Disease. The effects of etanercept on cognitive, behavioural, functional and immunological outcomes will be examined as secondary aims.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 41
• Est. primary completion date: December 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 55 Years and older

Eligibility

Inclusion Criteria:

• Male or female patients aged > 54 years

• Have a minimum of 7 years of education

• Be able to hear, read, write and perform study neuropsychological tests in English

• Have adequate visual and auditory acuity to allow neuropsychological testing based on the research clinician's judgement

• Fulfil Diagnostic & Statistical Manual (DSM-IV-TR)criteria for diagnosis of dementia of the Alzheimer type

• Have a diagnosis of probable Alzheimer's Disease (National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria)

• Mini Mental State Examination (MMSE) score < 27 and > 10 points.

• To be currently taking and have been taking a cholinesterase inhibitor for a minimum period of 3 months prior to the day of inclusion into the study or to have been not been taking a cholinesterase inhibitor for a minimum period of 3 months prior to the day of inclusion into the study

• Have an informant who spends at least 24 hours per week with the patient and may be a close friend or a neighbour, not necessarily a close relative, spouse, son or daughter. He/she should be the same throughout the study and should be present at all visits. If it becomes necessary, a change of informant can be made but this must be clearly documented.

Exclusion Criteria:

• Inability or refusal to provide informed consent from patient or caregiver

• Absence of informant

• Unlikely to cooperate in the study, not able to attend scheduled examinations and visits, or not able to follow study instructions

• Participation in another study with administration of any investigational drug in the previous 3 months or already enrolled in another study

• Parkinson's Disease, Dementia with Lewy Bodies or clinically significant Parkinsonian symptoms

• Vascular disorder (modified Hachinski Ischaemic Scale score > 4)

• Recent Transient Ischaemic Attack (TIA) - within the last 3 months

• Signs of major cerebrovascular disease on MRI or CT scan, if performed prior to entry into study (i.e. presence of infarction in greater than 25% of white matter, more than 1 lacune within basal ganglia, more than 2 lacunes in white matter)

• Any other previous or ongoing chronic or recurrent disease of the central nervous system, including demyelinating disease or psychiatric diseases, that may have an impact on cognitive performance, left to the research clinician's judgement

• Any of the following laboratory abnormalities at the screening visit:

i) Clinically significant Vitamin B12 levels less than the lower limit of normal ii) Clinically significant folate levels less than the lower limit of normal iii) Clinically significant thyroid-stimulating hormone (TSH) levels greater than the upper limit of normal and a clinically significant free thyroxine (FT4) level lower than the lower limit of normal

• Patients with previous or present history of severe or unstable medical conditions (e.g. hypertension, diabetes left to the research clinician's judgement)

• Current alcohol >35 units per week for men, or >28 units per week for women, or drug abuse at the discretion of the research clinician

• Surgical intervention planned during the study period.

• Treatment with immunosuppressive drugs and/or oral prednisone greater than 10mg/day within the past 90 days

• Treatment with Memantine within the past 3 months

• Vaccination or immunization with any live vaccine (eg: polio, rubella, yellow fever) or the pneumococcal vaccine within the past 30 days.

• Pregnancy or breast feeding.

• Severe hepatic, renal or cardiac disease.

• Previous use of a Tumour Necrosis Factor-alpha (TNFa) agent.

• Known skin photosensitivity.

• Infection in past 4 weeks or active infection.

• Heart failure: New York Heart Association (NYHA) Grade 3-4.

• History of blood disorders or current WCC = 3.5 x 109/l; platelet count = 100x109/l ; Hb = 10g/dl.

• Active or latent tuberculosis

• Rheumatoid arthritis; psoriasis; psoriatic arthritis or ankylosing spondylitis

• Septic arthritis in past 12 months

• Sepsis of prosthesis in past 12 months

• Chronic leg ulcers

• Indwelling urinary catheter

• Pulmonary fibrosis

• History of neoplasms / malignancies in past 5 years

• Pre-malignant conditions including Barrett's oesophagus; cervical dysplasia; large bowel polyps

• Any relevant acute or chronic abnormality detected during the physical and neurological examinations. Electrocardiogram (ECG) or laboratory tests likely to interfere with the study evaluations in the research clinician's judgement

• Previous exposure to amyloid vaccines, monoclonal antibodies or intravenous immunoglobulins meant to treat Alzheimer's disease

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Alzheimer Disease
• Alzheimer's Disease

Intervention

Biological:
• Etanercept
50 mg given as a once weekly subcutaneous injection

Other:
• Placebo
Placebo injection given once weekly

Locations

Country	Name	City	State
United Kingdom	Memory Assessment and Research Centre, Moorgreen Hospital	Southampton	Hampshire

Sponsors (3)

Lead Sponsor	Collaborator
University of Southampton	Hampshire Hospitals NHS Foundation Trust, Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of adverse events and serious adverse events (the study is a Phase II safety trial)		6 months	Yes
Secondary	Difference in change in Alzheimer's Disease Assessment Scale - Cognitive Section (ADAS-cog) total score between treated and placebo groups from baseline to end point at 6 months		6 months	No
Secondary	Difference in change in Neuropsychiatric Inventory (NPI) total score between treated and placebo groups from baseline to end point at 6 months		6 months	No
Secondary	Difference in change in Clinician's Global Impression of Change (CGIC) and Carer's Impression of Change (Carer-IC) total score between treated and placebo groups from baseline to end point at 6 months		6 months	No
Secondary	Difference in change in Mini-Mental State Examination (MMSE) total score between treated and placebo groups from baseline to end point at 6 months		6 months	No
Secondary	Difference in change in Sickness Behaviour Scale between treated and placebo groups from baseline to end point at 6 months		6 months	No
Secondary	To establish whether a pro-inflammatory baseline cytokine profile predicts better response to treatment with etanercept		6 months	No
Secondary	To examine the effects of etanercept on inflammatory markers in the cerebrospinal fluid (CSF) of patients with Alzheimer's disease, and the relationship of these factors with clinical outcome		6 months	No