• Data from oral presentation adds to growing body of evidence supporting the profile of PRX012, which is designed to target all aggregated forms of amyloid beta with high binding potency
  • Demonstrated 20-fold higher affinity to amyloid beta soluble protofibrils when compared to lecanemab
  • Clears pyroglutamate-modified amyloid beta at lower concentrations when compared to donanemab

DUBLIN, Ireland I March 31, 2023 I Prothena Corporation plc (NASDAQ:PRTA), a late-stage clinical biotechnology company with a robust pipeline of investigational therapeutics built on protein dysregulation expertise, today announced new preclinical data from its PRX012 program, a potential best-in-class anti-amyloid beta (Aβ) product candidate in development for the treatment of Alzheimer’s disease, at the 2023 International Conference on Alzheimer’s and Parkinson’s Diseases and related neurological disorders (AD/PD) in Gothenburg, Sweden.

To build a more in-depth understanding of the profile of PRX012 and its potential as a best-in-class anti-Aβ treatment for Alzheimer’s disease, two preclinical studies presented in an oral presentation at AD/PD 2023 compare a PRX012-surrogate* (PRX012s) to approved and investigational molecules. Surface Plasmon Resonance (SPR) was used to compare PRX012s to lecanemab+ and showed that PRX012s had approximately 20-fold higher affinity to Aβ protofibrils as compared to lecanemab when tested under the same conditions. This result was largely driven by a slower binding dissociation rate of PRX012s versus lecanemab.

The second study, an ex vivo study using post-mortem Alzheimer’s disease brain tissue, was designed to test the ability of PRX012s to clear pyroglutamate-modified Aβ deposited in plaques. Study results showed that lower concentrations of PRX012s induced more potent and robust clearance of pyroglutamate-modified Aβ as compared to donanemab+. In the experiment, microglia simultaneously phagocytosed non-pyroglutamate-modified Aβ and pyroglutamate-modified Aβ in the presence of PRX012s, indicating that high opsonization efficiency of plaques by PRX012s was sufficient to clear both forms of Aβ.

“These new preclinical data add to the scientific rationale of the PRX012 program, which has the potential to deliver a next-generation Alzheimer’s disease treatment and enable a more convenient administration for patients and caregivers,” said Wagner Zago, Ph.D., Chief Scientific Officer at Prothena. “With more than 55 million people worldwide estimated to be living with Alzheimer’s disease or other dementias, the timely delivery of improved disease modifying treatments is critical for these patients and their families. Prothena is committed to delivering a patient-centric, best-in-class Aβ-targeting antibody with the potential to robustly and safely deplete Aβ plaques.”

These data add to the growing body of evidence supporting the profile of PRX012, which is designed to target all aggregated forms of Aβ with high binding potency. The data further support the ongoing clinical development of PRX012 as a potential best-in-class treatment for Alzheimer’s disease that could enable improved access and more convenient administration for patients and caregivers.

Additional Prothena Activities at AD/DP 2023

Other activities at AD/PD 2023 showcased Prothena’s broad participation at this year’s congress bringing together thought leaders in Alzheimer’s disease research, including Prothena leadership, at a company-sponsored Symposium titled Entering the Era of Disease-Modifying Treatments for AD: Taking Stock of Today and Looking to Tomorrow. Two Forum Discussions, Immunotherapies in AD: From Basics to Approval and Anti-Tau Therapies in Clinical Trials also featured Prothena’s scientific leadership. Prothena’s prasinezumab development partner Roche also contributed poster and oral presentations highlighting aspects of the Phase 2 PASADENA study of prasinezumab for the treatment of Parkinson’s disease.

About PRX012

PRX012, an investigational next-generation anti-Aβ antibody, was designed as a subcutaneous IgG1 mAb to target multiple aggregated forms of Aβ, including protofibrils and plaques, with high binding affinity. PRX012 is currently being investigated in Phase 1 clinical studies for the treatment of Alzheimer’s disease. Preclinical data have demonstrated binding of PRX012 to beta amyloid plaques and oligomers with high affinity, resulting in effective Aβ plaque occupancy and removal at relatively lower antibody concentrations, potentially enabling lower volumes of administration for subcutaneous delivery. Preclinical data have also demonstrated clearance of both pyroglutamate modified and unmodified Aβ plaque in brain tissue at concentrations of PRX012 estimated to be clinically achievable in the central nervous system with subcutaneous delivery.

About Alzheimer’s Disease

Alzheimer’s disease is a fatal disease and the most common form of dementia causing increasingly serious symptoms, including confusion, disorientation, mood and behavioral changes, and difficulty speaking, swallowing, and walking. More than 55 million people worldwide are estimated to be living with Alzheimer’s disease or other dementias. Alzheimer’s disease is the most common neurodegenerative disorder. There is an urgent need for therapies that slow the progression and ultimately prevent Alzheimer’s disease to address this global healthcare crisis. Prothena’s Alzheimer’s disease portfolio spans next generation antibody immunotherapy, small molecule, and vaccine approaches, geared toward building upon first generation treatments to advance the treatment paradigm.

About Prasinezumab

Prasinezumab is a humanized monoclonal antibody that targets a carboxyl terminal epitope of alpha-synuclein, a protein found in neurons that can aggregate and spread from cell to cell, resulting in the neuronal dysfunction and loss that causes Parkinson’s disease. Prasinezumab is designed to block the cell-to-cell transmission of the aggregated, pathogenic forms of alpha-synuclein in Parkinson’s disease, thereby slowing clinical decline. In December 2013, Prothena and Roche entered into a worldwide collaboration to develop and commercialize antibodies that target alpha-synuclein, including prasinezumab. For more information on the Phase 2b PADOVA clinical study of prasinezumab in patients with early Parkinson’s disease, visit clinicaltrials.gov (NCT#04777331).

About Parkinson’s Disease

Parkinson’s disease is a progressive degenerative disorder of the entire nervous system that affects one in 100 people over age 60. An estimated seven to 10 million people are living with Parkinson’s disease worldwide. It is the second most common neurodegenerative disorder after Alzheimer’s disease. The disease is characterized by the neuronal accumulation of aggregated alpha-synuclein in the central nervous system and peripheral nervous system that results in a wide spectrum of worsening progressive motor and non-motor symptoms. While diagnosis relies on motor symptoms classically associated with Parkinson’s disease, non-motor symptoms may present many years earlier. Current treatments for Parkinson’s disease are symptomatic and only address a subset of symptoms such as motor impairment, dementia, or psychosis. There are currently no treatments available that target the underlying cause of the disease and can slow its progression.

About Prothena

Prothena Corporation plc is a late-stage clinical biotechnology company with expertise in protein dysregulation and a pipeline of investigational therapeutics with the potential to change the course of devastating neurodegenerative and rare peripheral amyloid diseases. Fueled by its deep scientific expertise built over decades of research, Prothena is advancing a pipeline of therapeutic candidates for a number of indications and novel targets for which its ability to integrate scientific insights around neurological dysfunction and the biology of misfolded proteins can be leveraged. Prothena’s pipeline includes both wholly-owned and partnered programs being developed for the potential treatment of diseases including AL amyloidosis, ATTR amyloidosis, Alzheimer’s disease, Parkinson’s disease and a number of other neurodegenerative diseases. For more information, please visit the Company’s website at www.prothena.com and follow the Company on Twitter @ProthenaCorp.

* “Surrogate” is defined as an antibody with >99.5% homology, the same binding epitope and equivalent binding profile to different forms of Aβ where directly compared.

+ Lecanemab and donanemab were generated from publicly available sequences.

SOURCE: Prothena