Primary Progressive Nonfluent Aphasia
Conditions
Keywords
tau, neurofibrillary, degeneration, primary progressive aphasia, agrammatic, tauopathy, immunotherapy, immunization
Brief summary
This study is a pilot trial evaluating the safety and immunogenicity of AADvac1 in patients with the non-fluent variant of Primary Progressive Aphasia. 50% of participants will receive the 40 µg dosage of AADvac1 and 50% of participants will receive the 160 µg dosage of AADvac1. No placebo is used.
Detailed description
The non-fluent variant of Primary progressive Aphasia (nfvPPA) is a chronic progressive neurodegenerative disorder of the brain. Over the course of the disease, pathological proteins accumulate in the brain, damaging neurons, thus causing them to lose their connections and die. No treatments are currently available; symptomatic medications are used off-label in nfvPPA. AADvac1 is designed to raise antibodies against pathological tau protein (the primary constituent of neurofibrillary pathology, which is the underlying cause of disease in \ 80% of nfvPPA cases). These antibodies are expected to prevent tau protein from aggregating, to facilitate the removal of tau protein aggregates and prevent the spreading of pathology, slowing or halting the progress of the disease.
Interventions
DRUGAADvac1 40 µg
Active immunotherapy against neurofibrillary pathology.
DRUGAADvac1 160 µg
Active immunotherapy against neurofibrillary pathology.
Sponsors
Axon Neuroscience SE
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Masking description
Patients are unaware of the dosage strength they are receiving. The AADvac1 vials are numbered, and the coding unknown to the patient. The investigator handles the vaccine vials and administers the IMP.
Intervention model description
Patients will be allocated to one of two dosage strengths of AADvac1. No placebo is used. No active comparator is used.
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
1. Patient has a clinical diagnosis of non-fluent/agrammatic variant PPA according to the criteria by Gorno-Tempini et al. (2011) with evidence of left frontal brain hypometabolism. Patients with right-sided hypometabolism are eligible for the study only if they are left-handed. 2. Patient has a FTLD-CDR language domain score of ≤ 2, and other individual FTLD-CDR domain scores ≤ 1. 3. Patient's age is 18 - 85 years inclusive at the time of having provided informed consent. 4. Patient has adequate visual and auditory abilities and premorbid local language skills to allow neuropsychological testing. 5. Sexually active female patients must be using highly effective contraception methods, or be surgically sterile, or be at least 2 years post-menopausal. 6. Sexually active male patients must be using highly effective contraception methods, or be surgically sterile. 7. Patient and caregiver have signed and dated written informed consent. 8. Availability of a partner/caregiver knowing the patient and being able to accompany the patient to the visits. 9. Patient is legally competent.
Exclusion criteria
1. The patient's brain MRI is incompatible with a diagnosis of nfvPPA. 2. Patient has a history or evidence of a central nervous system (CNS) disorder other than nfvPPA which may cause symptoms of aphasia or dementia (Alzheimer's disease, Dementia with Lewy Bodies, inflammatory/demyelinating CNS conditions, Creutzfeldt-Jakob disease, Huntington's disease, etc.) 3. Patient has a history or currently suffers from a significant psychiatric illness such as schizophrenia, any type of psychotic disorder or bipolar affective disorder. 4. Patient has a history or evidence of cerebrovascular disease (ischemic or haemorrhagic stroke), or diagnosis of possible, probable or definite vascular dementia. 5. Patient has Wernicke's encephalopathy. 6. Patient has metabolic or toxic encephalopathy or dementia due to a general medical condition. 7. Patient suffers from hypothyroidism, defined as 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 12 weeks before study entry. 8. Patient has a known pathogenic mutation in GRN or C9orf72. 9. Presence or history of allergy to components of the vaccine. 10. Presence and/or history of immunodeficiency (e.g., HIV). 11. Patient is currently being treated with immunosuppressive drugs. 12. 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. 13. Patient has a recent (≤ 5 years since last specific treatment) history of cancer (Exceptions: basal cell carcinoma, intraepithelial cervical neoplasia). 14. Patient has an active infectious disease (e.g., Hepatitis B, C). 15. Patient had a myocardial infarction within the last 2 years. 16. Patient has a current clinically important systemic illness that is likely to result in deterioration of the patient's condition or affect the subject's safety during the study: 1. poorly controlled congestive heart failure (New York Heart Association \[NYHA\] score ≥ 3), 2. poorly controlled diabetes, 3. severe renal insufficiency (Estimated glomerular filtration rate \< 30 mL/min), 4. chronic liver disease - ALT (alanine aminotransferase) \> 2x upper limit of normal range (ULN), AST (aspartate aminotransferase) \> 2x ULN 5. other clinically significant systemic illness, if considered relevant by the investigator. 17. Patient had alcohol or drug dependence within the past year. 18. Patient has a current diagnosis of epilepsy. 19. Pregnant or breastfeeding women. 20. Patient has participated in another interventional clinical trial within 12 weeks before Visit 01. 21. Patient has contraindication for MRI imaging such as metallic endoprosthesis or MRI-incompatible stent implantation. 22. Patient has contraindications for other study procedures, such as CSF sampling. 23. Patient had surgery (under general anaesthesia) within 12 weeks prior to Visit 01 and/or scheduled surgery (under general anaesthesia) during the whole study period. 24. Patient is currently being treated or was treated in the past with any active vaccines for a neurodegenerative disorder. 25. Patients not expected to complete the clinical trial. 26. Patient, in the opinion of the investigator, is unlikely to comply with the clinical study protocol, or is unsuitable for other reasons. 27. Patient is dependent from Sponsor or investigator (e.g. as an employee or as a relative).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] | 25 months | The safety assessment is based on the number, type and severity of adverse events (AEs). |
| Immunogenicity (Percentage of patients who develop an IgG immune response, geometric mean titre of titre of antibodies against Axon Peptide 108, IgG to IgM ratio of antibodies against Axon Peptide 108) | 24 months | AADvac1 depends on raising antibodies that mediate its treatment effects. Immunogenicity assessment includes: Percentage of AADvac1-treated patients who develop an immune response (responder rate), geometric mean titre of antibodies against Axon Peptide 108, IgG to IgM ratio of antibodies against Axon Peptide 108. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Magnetic resonance imaging (MRI) volumetry | 24 months | Temporal change in whole brain volume and set of regions of interest, as measured by MRI |
| Frontotemporal lobar degeneration - Clinical Dementia Rating - Sum of Boxes (FTLD-CDR-SB) | 24 months | Temporal change in FTLD-CDR SB score |
| Clinician's Global Impression - Improvement (CGI-I) | 24 months | Temporal change in CGI-I score |
| Instrumental Activities of Daily Living (IADL) | 24 months | Temporal change in Amsterdam IADL |
| Custom Cognitive Battery | 24 months | Temporal change in the custom Cognitive Battery score |
| Cerebrospinal fluid (CSF) biomarkers | 24 months | Temporal change in total CSF neurogranin, phosphorylated neurofilament heavy chain protein, ubiquitin, β-synuclein, tau protein, phospho-tau pT181, N-terminal tau protein, amyloid β1-40, amyloid-β1-42, ubiquitin, α-, β- and γ-synuclein, Chitinase-3-like protein (YKL-40), Monocyte chemoattractant protein-1 (MCP-1), and other CSF markers |
| Unified Parkinson's disease rating scale (UPDRS) part III | 24 months | Temporal change in UPDRS part III score |
| Frontal Systems Behavior Scale (FrSBe) | 24 months | Temporal change in FrSBe score |
| Immune cell (granulocyte, monocyte, and lymphocyte populations) | 24 months | Temporal change in immunological variables (monocytes, lymphocytes, basophil and neutrophil granulocytes; a range of lymphocyte sub-populations - CD3+, CD3+/CD4+, CD3+/CD4+/CD28+, CD3+/CD4+/CD28+/CD45RA+, CD3+/CD4+/CD28+/CD45RO+, CD3+/CD8+, CD3+/CD8+/CD28+, CD3+/CD8+/CD28+/CD45RA+, CD3+/CD8+/CD28+/CD45RO+) over 24 months |
| Correlation of a range of potential immunological predictors with IgG antibody titres against Axon Peptide 108 | 24 months | Correlation of measures of immune response with immunological variables (monocytes, lymphocytes, basophil and neutrophil granulocytes; a range of lymphocyte sub-populations - CD3+, CD3+/CD4+, CD3+/CD4+/CD28+, CD3+/CD4+/CD28+/CD45RA+, CD3+/CD4+/CD28+/CD45RO+, CD3+/CD8+, CD3+/CD8+/CD28+, CD3+/CD8+/CD28+/CD45RA+, CD3+/CD8+/CD28+/CD45RO+) will individually be assessed for correlation with IgG antibody titres. The possibility of multiple independent predictors of the antibody response will be examined using regression trees analysis) |
| Addenbrooke's Cognitive Examination | 24 months | Temporal change in Addenbrooke's Cognitive Examination score |
| Serum neurofilament light chain protein (and other blood biomarkers of nfvPPA) | 24 months | Temporal change in neurofilament light chain protein and other blood biomarkers (exploratory measure; biomarker panel to be finalised based on the state of the art at the time of analysis) |
Countries
Germany
Outcome results
None listed