Immunoadsorption for Treatment of Alzheimer's Disease (IMAD)

University Medicine Greifswald

Status

Terminated

Conditions

Alzheimer Dementia

Treatments

Device: Immunoadsorption with Globaffin

Study type

Interventional

Funder types

Other

Identifiers

NCT03132272

201503IMAD

CIV-16-02-014668 (Other Identifier)

Details and patient eligibility

About

Efficacy of immunoadsorption for treatment of persons with Alzheimer dementia and agonistic autoantibodies against alpha1A-adrenoceptor.

Full description

The IMAD trial outlined aims to ascertain whether the positive effects of immunoadsorption (IA) on slowing down dementia progression, shown in a pilot trial, can be replicated in a slightly larger number of subjects and to comprehensively investigate the effects by a combination of brain and vessel imaging along with cognitive tests and further state-of-the-art cardiovascular, cerebrovascular and laboratory examinations. If the trial results underpin the hypothesis that IA effectively counteracts pathophysiological impairments and dementia-related cognitive decline, it may open up a new treatment approach against dementia, namely the reversal or avoidance of further vascular damage by the removal of agonistic autoantibodies (agAAB) in agAAB-positive persons.

The aim of this study is (beside of safety) to demonstrate the stop of the vascular remodeling and cognition decline by immunoadsorption, a therapeutic method which is well established in cardiology and nephrology.

Enrollment

11 patients

Sex

All

Ages

55 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

55-85 years of age
Diagnosis of Alzheimer's disease
Presence of agAAB against alpha1-adrenoceptor
Mini mental state examination (MMSE) score between 19 and 26
Written informed consent given

Exclusion criteria

Haemanalysis:
- Presence of autoantibodies against the N-methyl-D-aspartate (NMDA) receptor
- Defective blood coagulation at time of inclusion
- Severe protein deficiency disorders
- manifest Vitamin/Folic acid deficiency (substitution allowed)
Active infectious disease, or signs of ongoing infection with C-reactive protein (CRP) >10mmol/L
Impaired renal function (serum creatinine >220 μmol/L)
Any disease requiring immunosuppressive drugs or therapeutic antibodies
Non curative treated malignant disease or another life-threatening disease with poor prognosis (survival less than 2 years), except for basal-cell carcinoma
Unstable angina pectoris, atrioventricular block (AV block) 2./3. degree or symptomatic sick sinus syndrome without implanted pacemaker, history of myocardial infarct, bypass or other revascularization measures, valvular heart defect (≥ 2. Degree)
Severely reduced left ventricular systolic function (LVEF < 30%) and/or heart failure symptoms according to New York Heart Association (NYHA) class III/IV
Clinical manifestation of arterial disease, vascular surgery: No Arteria Carotis Interna (ACI) Stenosis > 60%, peripheral artery occlusive disease (PAOD) > IIb, NASCET, no clinical manifest apparent stroke in anamnesis, MRI: no diffusion disorder, no expired territorial stroke
Endocrine disorder excluding diabetes mellitus
Severe hepatic damages (CHILD-Score < 4)
Severe mental disorders (bipolar disorder, schizophrenia, depression) requiring treatment
Alcohol or drug abuse
Drug therapy against dementia since less than 3 months
Psychopharmacological drug therapy since less than 3 months
Dialysis requirement
MRI contraindications (e.g. heart pacemaker)
Legal tutelage
Previous treatments with IA or immunoglobulin
Inability to undergo the study procedure (IA on five consecutive days with subsequent Immunoglobulin G (IgG) substitution)
treatment with angiotensin-converting-enzyme inhibitors (ACE inhibitors) during the IA (angiotensin receptor blockers (AT-blockers) possible)
Participation in any other clinical/interventional study within less than 30 days prior to screening date