Amylyx Pharmaceuticals to Present Updates on its AMX0114 and RELYVRIO® Programs in ALS at the 2024 Muscular Dystrophy Association (MDA) Clinical and Scientific Conference
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The development of AMX0114 by Amylyx Pharmaceuticals represents a significant step in the treatment of amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease that currently has limited therapeutic options. The focus on targeting calpain-2, a protein implicated in axonal degeneration, could potentially halt or slow the progression of ALS. The pre-clinical efficacy studies and the upcoming first-in-human study are critical milestones for the drug's development, which, if successful, could lead to a new treatment option for ALS patients.
Investors should be aware that the success of these clinical trials could have a substantial impact on the company's stock value. However, it is important to consider the inherent risks of drug development, particularly in the field of neurodegenerative diseases, where many promising compounds have failed in clinical trials. The long-term potential of AMX0114, therefore, hinges on both the scientific outcomes of the trials and the regulatory pathway ahead.
The pharmacokinetic and pharmacodynamic study of AMX0035, which is already approved to treat ALS in the U.S. and Canada, provides additional insight into the drug's safety profile and metabolic characteristics. The absence of new safety signals reinforces the drug's current market position and could influence prescribing patterns among neurologists. For investors, the continued accumulation of positive data around AMX0035 could support Amylyx's market capitalization and enhance investor confidence in the company's research and development capabilities.
Furthermore, the approval of AMX0035 in major markets not only generates revenue but also establishes Amylyx as a key player in the ALS treatment market. This could potentially attract partnerships or acquisition interest from larger pharmaceutical companies seeking to expand their neurology portfolios.
From a regulatory standpoint, the investigational new drug enabling studies for AMX0114 are a precursor to potential FDA approval processes. The design approach for the first-in-human study will need to adhere to stringent regulatory standards to ensure patient safety and robust data collection. It's crucial for stakeholders to understand that any deviations or negative findings in these early studies could significantly delay or halt the drug's development, impacting both the company's strategic direction and its financial health.
Moreover, the existing approvals for AMX0035, albeit with conditions in Canada, suggest that Amylyx has successfully navigated part of the complex regulatory landscape. This experience can be advantageous as they prepare for the clinical trials of AMX0114, though the legal and regulatory hurdles will remain substantial and require careful management.
Details of the poster presentations are as follows:
Title: Next Steps in Development for AMX0114: An Antisense Oligonucleotide Targeting Calpain-2, a Critical Effector of Axonal Degeneration
The Company is advancing AMX0114, our internally developed ASO targeting calpain-2, a critical effector of axonal degeneration in ALS and other neurodegenerative diseases, through investigational new drug enabling studies, with the goal of entering the clinic in 2024. This poster shares details on pre-clinical efficacy studies as well as introduces the design approach for the first-in-human study, anticipated to begin later this year. The Company is studying multiple cellular pathways implicated in disease pathogenesis as we believe that it is going to take a combination approach to find a cure for ALS.
Date and Time: March 4, 2024, from 6:00PM – 8:00PM EST
Title: Findings From a Pharmacokinetic and Pharmacodynamic Study of Sodium Phenylbutyrate and Taurursodiol in Participants With Amyotrophic Lateral Sclerosis
This poster provides results from a Phase 2a, open-label, sequential period study of AMX0035 pharmacokinetics in participants with ALS and includes safety data in addition to pharmacokinetics of AMX0035 and its major metabolites. No new safety signals were identified during this study.
Date and Time: March 4, 2024, from 6:00PM – 8:00PM EST
For conference information, visit: https://www.mdaconference.org/
Additional information, including copies of the poster presentations, will be made available on the “Publications” tab of the Amylyx website, following the conclusion of the poster presentations.
About RELYVRIO®/ ALBRIOZA™ / ALBRIOZA® / AMX0035
RELYVRIO®, an oral, fixed-dose combination of sodium phenylbutyrate and taurursodiol (known as ursodoxicoltaurine outside of the
RELYVRIO® (sodium phenylbutyrate and taurursodiol) Safety Information for
WARNINGS AND PRECAUTIONS
Risk in Patients with Enterohepatic Circulation Disorders, Pancreatic Disorders, or Intestinal Disorders
RELYVRIO contains taurursodiol, which is a bile acid. In patients with disorders that interfere with bile acid circulation, there may be an increased risk for worsening diarrhea, and patients should be monitored appropriately for this adverse reaction. Pancreatic insufficiency, intestinal malabsorption, or intestinal diseases that may alter the concentration of bile acids may also lead to decreased absorption of either of the components of RELYVRIO. Because different enterohepatic circulation, pancreatic, and intestinal disorders have varying degrees of severity, consider consulting with a specialist. Patients with disorders of enterohepatic circulation (e.g., biliary infection, active cholecystitis), severe pancreatic disorders (e.g., pancreatitis), and intestinal disorders that may alter concentrations of bile acids (e.g., ileal resection, regional ileitis) were excluded from the study; therefore, there is no clinical experience in these conditions.
Use in Patients Sensitive to High Sodium Intake
RELYVRIO has a high salt content. Each initial daily dosage of 1 packet contains 464 mg of sodium; each maintenance dosage of 2 packets daily contains 928 mg of sodium. In patients sensitive to salt intake (e.g., those with heart failure, hypertension, or renal impairment), consider the amount of daily sodium intake in each dose of RELYVRIO and monitor appropriately.
ADVERSE REACTIONS
The most common adverse reactions (at least
Please click here for RELYVRIO Full
About Amylyx Pharmaceuticals
Amylyx Pharmaceuticals, Inc. is committed to supporting and creating more moments for the neurodegenerative community through the discovery and development of innovative new treatments. Amylyx is headquartered in
Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, the potential of AMX0114 as a treatment for ALS and the Company’s plans to develop AMX0114, the potential of AMX0035 as a treatment for ALS and the Company’s plans to explore the use of AMX0035 for other neurodegenerative diseases including PSP, the timelines for the ORION study in PSP, and expectations regarding our longer-term strategy. Any forward-looking statements in this press release are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Risks that contribute to the uncertain nature of the forward-looking statements include: Amylyx’ ability to fund operations, the success, cost, and timing of Amylyx’ program development activities, Amylyx’ ability to execute on its commercial and regulatory strategy, regulatory developments, expectations regarding the timing and outcome of EMA’s review of AMX0035 for the treatment of ALS, Amylyx’ reliance on third parties, including to conduct clinical trials and manufacture products, and the effect of global economic uncertainty and financial market volatility caused by economic effects of rising inflation and interest rates, the COVID-19 pandemic, geopolitical instability, changes in international trade relationships and military conflicts, as well as the risks and uncertainties set forth in Amylyx’ United States Securities and Exchange Commission (SEC) filings, including Amylyx’ Quarterly Report on Form 10-Q for the quarter ended September 30, 2023, and subsequent filings with the SEC. All forward-looking statements contained in this press release speak only as of the date on which they were made. Subject to any obligations under applicable law, Amylyx undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.
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Media
Amylyx Media Team
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Investors
Lindsey Allen
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Investors@amylyx.com
Source: Amylyx Pharmaceuticals, Inc.
