Seven presentations by AC Immune and its partners at AAT-AD/PD™
New data on early-stage TDP-43 and alpha-synuclein therapeutic and diagnostic candidates
A lead anti-alpha-synuclein therapeutic antibody candidate has advanced into preclinical development to treat Parkinson’s disease and other synucleinopathies
LAUSANNE, Switzerland I April 02, 2020 I AC Immune SA (NASDAQ: ACIU), a Swiss-based, clinical-stage biopharmaceutical company today outlined new preclinical data that will be presented at this year’s first ever online AAT-AD/PD™ Focus Meeting from April 2–5, 2020. The presentations describe proof-of-concept preclinical data for lead candidates in AC Immune’s therapeutic and diagnostic programs targeting TDP-43 and alpha-synuclein. These pathological proteins represent targets of increasing interest for the treatment of neurodegenerative diseases, and AC Immune’s programs are amongst the most advanced in the field.
Prof. Andrea Pfeifer, CEO of AC Immune SA, commented: “Our heritage as a leader in delivering cutting-edge science and our strong cash position provides the foundation to continue advancing data on novel targets for neurodegenerative diseases. The aggregation of pathological forms of TDP-43 and alpha-synuclein proteins are hallmarks of numerous neurodegenerative diseases, including neuroOrphan indications such as frontotemporal lobar degeneration, amyotrophic lateral sclerosis and multiple system atrophy. As novel therapeutic targets in Alzheimer’s disease (AD), it has been shown that patients with a high degree of Abeta and Tau pathologies also show a high level of alpha-synuclein and/or TDP-43 co-pathology.”
Prof. Pfeifer continued: “The prevalence of co-pathologies in AD and other neurodegenerative diseases highlights the need for the precision medicine pioneered by AC Immune and the opportunity for earlier and more accurate diagnosis. As one of the most advanced programs targeting TDP-43, with in vivo proof-of-concept data, we intend to develop our antibody candidate in a neuroOrphan indication. Leading the way in developing the first TDP-43 positron emission tomography (PET) imaging agent, we hope to improve the timing and accuracy of diagnoses in neurodegenerative disease, representing our complementary diagnostics portfolio.”
TDP-43 and alpha-synuclein pathologies have been shown to start from a focal point in the brain and progressively spread to other brain regions with disease progression. Antibody-mediated clearance of pathological TDP-43 and alpha-synuclein represent attractive strategies for therapeutic intervention. Availability of non-invasive tools like PET imaging agents would allow accurate diagnosis and monitoring of disease progression, and would potentially enable longitudinal drug efficacy measurements in patients.
The three preclinical studies that will be presented at AAT-AD/PD™ illustrate how AC Immune continues to leverage its proprietary technology platforms, SupraAntigen™ and Morphomer™ to develop product candidates against pathologies associated with TDP-43 and alpha-synuclein.
Anti-TDP-43 antibody
Data to be presented for the first time, shows that the Company’s lead TDP-43 antibody candidate mitigated TDP-43 neuropathology in a mouse model of TDP-43 proteinopathies. The unique pool of TDP-43 antibodies generated by AC Immune’s proprietary SupraAntigen™ platform also allowed development of highly sensitive assays for detection and quantification of total and disease-specific TDP-43 isoforms in biofluids with the potential for clinical biomarker evaluation.
Morphomer™ TDP-43 imaging
Data for a first in class TDP-43 PET tracer will illustrate how the lead candidate was identified and optimized. The lead candidate, generated using the proprietary Morphomer™ platform, demonstrates binding to brain-derived pathological TDP-43 aggregates with high affinity and, importantly, direct target engagement on patient brain tissue.
Anti-alpha-synuclein antibody
Using the SupraAntigen™ platform, antibodies with high-affinity for aggregated alpha-synuclein have been developed which prevent the intercellular spreading of toxic alpha-synuclein species. Data, presented for the first time, demonstrate that lead candidate antibodies reduce the de novo formation of alpha-synuclein aggregates in vitro and significantly decrease spreading of alpha-synuclein pathology in a mouse model of human disease. A lead therapeutic candidate has been advanced into preclinical development to treat Parkinson’s disease and other synucleinopathies.
Prof. Pfeifer added: “AC Immune continues to deliver on its Roadmap to Successful Therapies for Neurodegenerative Diseases, enabling precision medicine by selecting clinical study populations based on the presence of the underlying proteinopathies.”
AAT-AD/PD™ features seven presentations by AC Immune and its partners:
- Exploratory analysis of biomarker data from Phase 2/3 crenezumab studies using the neurotoolkit assay panel
Date: April 2, 2020 | 11:40 – 12:00 am CET
Presenter: Oral presentation Christina Rabe (Roche program)
- 18F-PI2620 Tau-PET for assessment of heterogeneous neuropathology in corticobasal syndrome
Date: April 2, 2020 | 12:40 – 1:00 pm CET
Presenter: Oral presentation by Carla Palleis (Life Molecular Imaging program)
- Development of ACI-35.030, a second generation anti-phospho tau vaccine, in clinical evaluation for the treatment of Alzheimer’s disease
Date: April 2, 2020 | 6:15 – 6:35 pm CET
Presenter: Oral presentation by Marija Vukicevic
- Monoclonal antibody targeting TDP-43 mitigates associated neuropathology in mouse model of TDP-43 proteinopathy
Date: April 3, 2020 | 3:10 – 3:30 pm CET
Presenter: Oral presentation Tariq Afroz
- Discovery and optimization of candidates for molecular imaging of TDP-43 proteinopathies
Date: April 3, 2020 | 9:29 – 9:35 am CET
Presenter: Short oral poster presentation by Tariq Afroz
- 18F-PI-2620 Tau PET is associated with beta-amyloid in MCI or mild-AD dementia subjects from the elenbecestat Mission AD program
Date: April 3, 2020 | 5:50 – 6:10 pm CET
Presenter: Oral presentation Andrew Stephens (Life Molecular Imaging program)
- Targeting spreading of pathological alpha-synuclein to treat Parkinson’s disease
Date: April 5, 2020 | 8:55 – 9:15 am CET
Presenter: Oral presentation Elpida Tsika
AC Immune’s presentations are available to download from the AAT-AD/PD™ website for those registered to attend the congress.
About AC Immune SA
AC Immune SA is a Nasdaq-listed clinical-stage biopharmaceutical company, which aims to become a global leader in precision medicine for neurodegenerative diseases. The Company utilizes two proprietary platforms, SupraAntigen™ and Morphomer™, to design, discover and develop small molecule and biological therapeutics as well as diagnostic products intended to diagnose, prevent and modify neurodegenerative diseases caused by misfolding proteins. The Company’s pipeline features nine therapeutic and three diagnostic product candidates, with six currently in clinical trials. It has collaborations with major pharmaceutical companies including Roche/Genentech, Lilly and Janssen.
SOURCE: AC Immune
Post Views: 24
Seven presentations by AC Immune and its partners at AAT-AD/PD™
New data on early-stage TDP-43 and alpha-synuclein therapeutic and diagnostic candidates
A lead anti-alpha-synuclein therapeutic antibody candidate has advanced into preclinical development to treat Parkinson’s disease and other synucleinopathies
LAUSANNE, Switzerland I April 02, 2020 I AC Immune SA (NASDAQ: ACIU), a Swiss-based, clinical-stage biopharmaceutical company today outlined new preclinical data that will be presented at this year’s first ever online AAT-AD/PD™ Focus Meeting from April 2–5, 2020. The presentations describe proof-of-concept preclinical data for lead candidates in AC Immune’s therapeutic and diagnostic programs targeting TDP-43 and alpha-synuclein. These pathological proteins represent targets of increasing interest for the treatment of neurodegenerative diseases, and AC Immune’s programs are amongst the most advanced in the field.
Prof. Andrea Pfeifer, CEO of AC Immune SA, commented: “Our heritage as a leader in delivering cutting-edge science and our strong cash position provides the foundation to continue advancing data on novel targets for neurodegenerative diseases. The aggregation of pathological forms of TDP-43 and alpha-synuclein proteins are hallmarks of numerous neurodegenerative diseases, including neuroOrphan indications such as frontotemporal lobar degeneration, amyotrophic lateral sclerosis and multiple system atrophy. As novel therapeutic targets in Alzheimer’s disease (AD), it has been shown that patients with a high degree of Abeta and Tau pathologies also show a high level of alpha-synuclein and/or TDP-43 co-pathology.”
Prof. Pfeifer continued: “The prevalence of co-pathologies in AD and other neurodegenerative diseases highlights the need for the precision medicine pioneered by AC Immune and the opportunity for earlier and more accurate diagnosis. As one of the most advanced programs targeting TDP-43, with in vivo proof-of-concept data, we intend to develop our antibody candidate in a neuroOrphan indication. Leading the way in developing the first TDP-43 positron emission tomography (PET) imaging agent, we hope to improve the timing and accuracy of diagnoses in neurodegenerative disease, representing our complementary diagnostics portfolio.”
TDP-43 and alpha-synuclein pathologies have been shown to start from a focal point in the brain and progressively spread to other brain regions with disease progression. Antibody-mediated clearance of pathological TDP-43 and alpha-synuclein represent attractive strategies for therapeutic intervention. Availability of non-invasive tools like PET imaging agents would allow accurate diagnosis and monitoring of disease progression, and would potentially enable longitudinal drug efficacy measurements in patients.
The three preclinical studies that will be presented at AAT-AD/PD™ illustrate how AC Immune continues to leverage its proprietary technology platforms, SupraAntigen™ and Morphomer™ to develop product candidates against pathologies associated with TDP-43 and alpha-synuclein.
Anti-TDP-43 antibody
Data to be presented for the first time, shows that the Company’s lead TDP-43 antibody candidate mitigated TDP-43 neuropathology in a mouse model of TDP-43 proteinopathies. The unique pool of TDP-43 antibodies generated by AC Immune’s proprietary SupraAntigen™ platform also allowed development of highly sensitive assays for detection and quantification of total and disease-specific TDP-43 isoforms in biofluids with the potential for clinical biomarker evaluation.
Morphomer™ TDP-43 imaging
Data for a first in class TDP-43 PET tracer will illustrate how the lead candidate was identified and optimized. The lead candidate, generated using the proprietary Morphomer™ platform, demonstrates binding to brain-derived pathological TDP-43 aggregates with high affinity and, importantly, direct target engagement on patient brain tissue.
Anti-alpha-synuclein antibody
Using the SupraAntigen™ platform, antibodies with high-affinity for aggregated alpha-synuclein have been developed which prevent the intercellular spreading of toxic alpha-synuclein species. Data, presented for the first time, demonstrate that lead candidate antibodies reduce the de novo formation of alpha-synuclein aggregates in vitro and significantly decrease spreading of alpha-synuclein pathology in a mouse model of human disease. A lead therapeutic candidate has been advanced into preclinical development to treat Parkinson’s disease and other synucleinopathies.
Prof. Pfeifer added: “AC Immune continues to deliver on its Roadmap to Successful Therapies for Neurodegenerative Diseases, enabling precision medicine by selecting clinical study populations based on the presence of the underlying proteinopathies.”
AAT-AD/PD™ features seven presentations by AC Immune and its partners:
- Exploratory analysis of biomarker data from Phase 2/3 crenezumab studies using the neurotoolkit assay panel
Date: April 2, 2020 | 11:40 – 12:00 am CET
Presenter: Oral presentation Christina Rabe (Roche program)
- 18F-PI2620 Tau-PET for assessment of heterogeneous neuropathology in corticobasal syndrome
Date: April 2, 2020 | 12:40 – 1:00 pm CET
Presenter: Oral presentation by Carla Palleis (Life Molecular Imaging program)
- Development of ACI-35.030, a second generation anti-phospho tau vaccine, in clinical evaluation for the treatment of Alzheimer’s disease
Date: April 2, 2020 | 6:15 – 6:35 pm CET
Presenter: Oral presentation by Marija Vukicevic
- Monoclonal antibody targeting TDP-43 mitigates associated neuropathology in mouse model of TDP-43 proteinopathy
Date: April 3, 2020 | 3:10 – 3:30 pm CET
Presenter: Oral presentation Tariq Afroz
- Discovery and optimization of candidates for molecular imaging of TDP-43 proteinopathies
Date: April 3, 2020 | 9:29 – 9:35 am CET
Presenter: Short oral poster presentation by Tariq Afroz
- 18F-PI-2620 Tau PET is associated with beta-amyloid in MCI or mild-AD dementia subjects from the elenbecestat Mission AD program
Date: April 3, 2020 | 5:50 – 6:10 pm CET
Presenter: Oral presentation Andrew Stephens (Life Molecular Imaging program)
- Targeting spreading of pathological alpha-synuclein to treat Parkinson’s disease
Date: April 5, 2020 | 8:55 – 9:15 am CET
Presenter: Oral presentation Elpida Tsika
AC Immune’s presentations are available to download from the AAT-AD/PD™ website for those registered to attend the congress.
About AC Immune SA
AC Immune SA is a Nasdaq-listed clinical-stage biopharmaceutical company, which aims to become a global leader in precision medicine for neurodegenerative diseases. The Company utilizes two proprietary platforms, SupraAntigen™ and Morphomer™, to design, discover and develop small molecule and biological therapeutics as well as diagnostic products intended to diagnose, prevent and modify neurodegenerative diseases caused by misfolding proteins. The Company’s pipeline features nine therapeutic and three diagnostic product candidates, with six currently in clinical trials. It has collaborations with major pharmaceutical companies including Roche/Genentech, Lilly and Janssen.
SOURCE: AC Immune
Post Views: 24
