🎈 Up Big Today: Find today's biggest gainers with our free screenerTry Stock Screener

FDA clears Astria Therapeutics' new AD drug for trial

Published 12/10/2024, 08:13 AM
ATXS
-

The press release contains forward-looking statements regarding the potential for STAR-0310 to be a leading treatment for AD and the expected timelines for clinical trials and results. These statements are based on Astria's current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially. InvestingPro analysis shows the stock has delivered an impressive 86% return over the past year, with analyst price targets ranging from $16 to $35, suggesting significant upside potential. The company maintains a healthy current ratio of 22.38, indicating strong short-term financial stability. For deeper insights into Astria's financial health and additional ProTips, investors can access comprehensive analysis through InvestingPro. InvestingPro analysis shows the stock has delivered an impressive 86% return over the past year, with analyst price targets ranging from $16 to $35, suggesting significant upside potential. The company maintains a healthy current ratio of 22.38, indicating strong short-term financial stability. For deeper insights into Astria's financial health and additional ProTips, investors can access comprehensive analysis through InvestingPro.

Chris Morabito, M.D., Chief Medical (TASE:PMCN) Officer at Astria Therapeutics, expressed optimism about the potential of the OX40 mechanism, which STAR-0310 targets. He noted that the antibody has been engineered with high affinity and potency, and low antibody-dependent cell-mediated cytotoxicity (ADCC), which could allow for an extended therapeutic window. Morabito also mentioned that the drug has the potential to be administered as infrequently as every six months due to its long half-life, which could offer a more convenient treatment schedule for patients.

The Phase 1a trial's initiation and the subsequent proof-of-concept study in AD patients, expected in the second quarter of 2026, represent significant milestones for the company. These studies aim to explore the efficacy and safety of STAR-0310, which, if successful, could lead to new treatment options for individuals with atopic dermatitis.

Astria Therapeutics focuses on developing therapies for allergic and immunologic diseases. Their lead program, navenibart (STAR-0215), is a monoclonal antibody inhibitor currently in clinical development for the treatment of hereditary angioedema.

The press release contains forward-looking statements regarding the potential for STAR-0310 to be a leading treatment for AD and the expected timelines for clinical trials and results. These statements are based on Astria's current expectations and are subject to various risks and uncertainties that could cause actual results to differ materially.

Investors and potential investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date they were made. The company does not undertake any obligation to publicly update or revise any forward-looking statements, except as required by law. This article is based on a press release statement from Astria Therapeutics.

In other recent news, Astria Therapeutics is drawing attention with significant developments. Anticipation is growing for the upcoming disclosure of the 6-month Phase Ib/II results for navenibart, the company's investigational therapy. TD Cowen has maintained a Buy rating, confident about the therapy's potential. The firm's optimism is supported by positive feedback from Key Opinion Leaders, who have expressed belief in the therapy's efficacy and safety profile.

Astria Therapeutics has also gained Orphan Medicinal Product Designation from the European Commission for navenibart, intended for hereditary angioedema (HAE) treatment. This follows positive Phase 1b/2 clinical trial results and the FDA's recognition of navenibart as an orphan drug in the United States. The company plans to advance navenibart into a Phase 3 trial in the first quarter of 2025.

In terms of analyst notes, H.C. Wainwright and TD Cowen have maintained their Buy ratings for Astria, emphasizing the potential of navenibart. Oppenheimer has raised its stock target for the company from $25 to $26, maintaining an Outperform rating, despite a higher than expected second-quarter loss. Astria Therapeutics has also partnered with Ypsomed AG for the development of an autoinjector for navenibart, aiming to provide patients with a user-friendly administration method. The company ended the quarter with around $355 million in cash reserves, expected to sustain operations through mid-2027. These are recent developments in the company's journey.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

Latest comments

Risk Disclosure: Trading in financial instruments and/or cryptocurrencies involves high risks including the risk of losing some, or all, of your investment amount, and may not be suitable for all investors. Prices of cryptocurrencies are extremely volatile and may be affected by external factors such as financial, regulatory or political events. Trading on margin increases the financial risks.
Before deciding to trade in financial instrument or cryptocurrencies you should be fully informed of the risks and costs associated with trading the financial markets, carefully consider your investment objectives, level of experience, and risk appetite, and seek professional advice where needed.
Fusion Media would like to remind you that the data contained in this website is not necessarily real-time nor accurate. The data and prices on the website are not necessarily provided by any market or exchange, but may be provided by market makers, and so prices may not be accurate and may differ from the actual price at any given market, meaning prices are indicative and not appropriate for trading purposes. Fusion Media and any provider of the data contained in this website will not accept liability for any loss or damage as a result of your trading, or your reliance on the information contained within this website.
It is prohibited to use, store, reproduce, display, modify, transmit or distribute the data contained in this website without the explicit prior written permission of Fusion Media and/or the data provider. All intellectual property rights are reserved by the providers and/or the exchange providing the data contained in this website.
Fusion Media may be compensated by the advertisers that appear on the website, based on your interaction with the advertisements or advertisers.
© 2007-2024 - Fusion Media Limited. All Rights Reserved.