24 Months Safety and Efficacy Study of AADvac1 in Patients With Mild Alzheimer's Disease (ADAMANT)
Alzheimer's Disease
About this trial
This is an interventional treatment trial for Alzheimer's Disease focused on measuring vaccine, tau protein, active, immunization, KLH, immunotherapy, tau
Eligibility Criteria
Inclusion criteria (abbreviated):
- Diagnosis of probable Alzheimer's disease according to the revised National Institute on Aging-Alzheimer's Association (NIA-AA) criteria (McKhann 2011).
- Mini Mental State Examination (MMSE) score ≥ 20 and ≤ 26.
- Brain MRI finding consistent with the diagnosis of Alzheimer's disease
- Medial temporal lobe atrophy: Scheltens score of ≥ 2 (on a scale of 0-4 on the more atrophied side) AND/OR positive AD biomarker profile in the CSF (amyloid+, tau+)
- At least 6 years of formal elementary education.
- Age 50-85 years.
- Fluency in the local language and sufficient auditory and visual capacities to allow neuropsychological testing.
- Ability to read and understand the informed consent.
- Stable therapy with an acetylcholinesterase inhibitor for at least 3 months prior to screening.
- If the patient is on memantine treatment, the dose regimen must be stable for at least 3 months prior to screening.
- Hachinski Ischemia Scale score ≤ 4.
- Availability of a caregiver.
- Female patients must be either surgically sterile or at least 2 years postmenopausal.
- Male patients must either be surgically sterile, or he and his female spouse/partner who is of childbearing potential must be using highly effective contraception starting at screening and continuing throughout the study period.
- Patient provides written informed consent.
Exclusion criteria (abbreviated):
- Participation in another clinical study within 3 months prior to screening.
- Pregnant or breastfeeding female.
- Not expected to complete the clinical study.
- Known allergy to components of the vaccine.
- Contraindication for MRI imaging.
Any of the following detected by brain MRI:
- Infarction in the territory of large vessels
- More than one lacunar infarct.
- Any lacunar infarct in a strategically important location.
- Confluent hemispheric deep white matter lesions (Fazekas grade 3).
- Other focal lesions which may be responsible for the cognitive status of the patient or any other abnormalities associated with significant central nervous disease other than Alzheimer's disease.
- Surgery (under general anaesthesia) within 3 months prior to screening and/or scheduled surgery (under general anaesthesia) during the whole study period.
- Patient has a history and/or currently suffers from a clinically significant autoimmune disease, or is expected to receive immunosuppressive or immunomodulatory treatment at the present or in the future.
- Recent history of cancer (last specific treatment ≤ 5 years prior to Screening).
- Myocardial infarction within 2 years prior to screening.
- Hepatitis B, C, HIV or Syphilis.
- Active infectious disease.
- Presence and/or history of immunodeficiency.
Patient currently suffering from a clinically important systemic illness:
- poorly controlled congestive heart failure (NYHA ≥ 3)
- BMI > 40
- poorly controlled diabetes (HbA1c > 7.5%)
- severe renal insufficiency (eGFR < 30 mL/min)
- chronic liver disease - ALT (alanine aminotransferase) > 66 U/L in females or > 80 U/L in males, AST (aspartate aminotransferase) > 82 U/L
- QTc interval prolongation in ECG (> 450 ms)
- other clinically significant systemic illness, if considered relevant by the investigator
- Hypothyroidism, defined as TSH (thyroid-stimulating hormone) elevation > 5.000 mcIU/mL, and/or FT4 levels < 0.7 ng/dL. Patients with corrected hypothyroidism are eligible for the study provided that treatment has been stable for 3 months before study entry.
- Valid diagnosis of a significant psychiatric illness such as schizophrenia, any type of psychotic disorder or bipolar affective disorder.
- Current depressive episode (Geriatric Depression Scale GDS ≥ 6) or major depressive episode within the last 1 years.
- Metabolic or toxic encephalopathy or dementia due to a general medical condition.
- History of alcohol or drug abuse or dependence within the past 2 years.
- Wernicke's encephalopathy.
- History or evidence of any CNS disorder other than AD that could be the cause of dementia.
- Cerebrovascular disease (ischemic or haemorrhagic stroke), or diagnosis of possible, probable or definite vascular dementia.
- Epilepsy.
- Treatment with experimental immunotherapeutics including intravenous immunoglobulin within 3 months prior to screening.
- Treatment with experimental therapies for AD aiming at disease-modification within 3 months prior to screening.
- Patient is currently being treated or was treated in the past with any active vaccines for AD.
- Treatment with immunosuppressive drugs.
- Change in dose of previous and current medications within the last 30 days prior to Screening (V01), if considered clinically relevant by the investigator.
- Vitamin B12 deficiency (serum vitamin B12 < 191 pg/mL).
Sites / Locations
- Ordination Dr. Bancher
- Universitätsklinik für Neurologie
- Abteilung Psychiatrie und Psychotherapie, LKH Hall
- Universitätsklinikum Innsbruck
- Fakultni nemocnice u sv. Anny v Brne, Mezinarodni centrum klinickeho vyzkumu (ICRC), Centrum pro kognitivni poruchy, Neuro 2
- Fakultni nemocnice Hradec Kralove, Neurologicka Klinika
- Narodni ustav dusevniho zdravi (NÚDZ), Department of cognitive disorders - AD Center
- Vseobecna fakultni nemocnice v Praze
- Fakultni nemocnice v Motole
- Neuro Centrum Odenwald
- Arzneimittelforschung Leipzig (AFL)
- Universität Heidelberg, Zentralinstitut für Seelische Gesundheit
- Klinikum rechts der Isar der Technischen Universität München, Klinik und Poliklinik fur Psychiatrie und Psychotherapie
- Praxis Dr. Klaus Christian Steinwachs
- Universitätsklinikum Ulm, Klinik und Poliklinik für Neurologie
- Podlaskie Centrum Psychogeriatrii
- Pallmed prowadzacy NZOZ Dom Sue Ryder w Bydgoszczy Centrum Psychoneurologii Wieku Podeszlego
- Wielospecjalistyczna Poradnia Lekarska Synapsis
- Care Clinic
- Centrum Neurologii Klinicznej, Krakowska Akademia Neurologii
- KO-MED Centra Kliniczne Sp. z o.o.
- Oddzial Neurologiczny
- NZOZ Neuro-Kard
- EUROMEDIS Sp. z o.o.
- Centrum Medyczne NeuroProtect
- Wrocławskie Centrum Alzheimerowskie
- "Dr. Constantin Gorgos" Psychiatry Hospital Titan
- Neurologicka ambulancia
- Nestatna psychiatricka ambulancia
- Univerzitna nemocnica Bratislava, Nemocnica Stare Mesto, I. Neurologicka klinika LF UK a UNB
- Univerzitna nemocnica Bratislava, Psychiatricka klinika LFUK a UNB
- Univerzitna nemocnica L Pasteura Kosice, Psychiatricka klinika
- NEURES, s.r.o. Neurologicka ambulancia
- Centrum zdravia R.B.K., s.r.o., Psychiatricka ambulancia
- Pro Mente Sana S.R.O., Psychiatricka Ambulancia
- Fakultna nemocnica s poliklinikou Zilina, Psychiatricke oddelenie
- Univerzitetni klinični Center Ljubljana, Neurology Clinic
- University Clinical Centre Maribor
- Skånes Universitetssjukhus Malmö, Minneskliniken
- Sahlgrenska Universitetssjukhuset, Minnesmottagningen
- Karolinska Universitetssjukhuset Huddinge
- Akademiska Sjukhuset I Uppsala, Minnes-och geriatrikmottagningen
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
AADvac1
Placebo
AADvac1 is a suspension for subcutaneous injection. AADvac1 is provided in single-use vials. Dosage: 40 µg Axon peptide 108 (coupled to keyhole limpet haemocyanin (KLH)) using aluminium hydroxide (containing 0.5 mg Al3+) as adjuvant, in a phosphate buffer. Patients receive 6 doses in 4-week intervals, and then 5 individual booster doses in 3-month intervals, for a total of 11 doses.
Placebo is a suspension for subcutaneous injection. Placebo is provided in single-use vials. Dosage: aluminium hydroxide (containing 0.5 mg Al3+), in a phosphate buffer. Patients receive 6 doses in 4-week intervals, and then 5 individual booster doses in 3-month intervals, for a total of 11 doses.