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Better Therapeutics Announces Acceptance of Late Breaking Abstract for Its AspyreRx Pivotal Trial 180 Day Outcomes and Participation at the 17th International Conference on Advanced Technologies & Treatments for Diabetes (ATTD)

Better Therapeutics Announces Acceptance of Late Breaking Abstract for Its AspyreRx Pivotal Trial 180 Day Outcomes and Participation at the 17th International Conference on Advanced Technologies & Treatments for Diabetes (ATTD)

Better Therapeutics宣佈接受其AspyrerX Pivotal試驗180天結果的最新摘要,並參加第17屆糖尿病先進技術與治療國際會議(ATTD)
Better Therapeutics ·  03/04 13:00

Company to host sponsored education session on Saturday, March 09, 2024; Expanding access to a high quality and effective lifestyle modification intervention

公司將於2024年3月9日星期六舉辦贊助的教育會議;擴大獲得高質量和有效的生活方式改變干預措施的機會

SAN FRANCISCO--(BUSINESS WIRE)--Mar. 4, 2024-- Better Therapeutics, Inc. (NASDAQ: BTTX), a pioneer in developing prescription digital therapeutics (PDTs) for treating cardiometabolic diseases, today announced the acceptance of a late-breaking abstract presenting 180-day outcomes data and its participation at the 17th International Conference on Advanced Technologies & Treatments for Diabetes (ATTD), to be held from March 6 to 9, 2024, in Florence, Italy. ATTD serves as a premier international forum showcasing cutting-edge advancements in diabetes care, bringing together clinicians, researchers, industry leaders, and policymakers from around the world to exchange knowledge and foster collaboration in the pursuit of innovative solutions for diabetes management.

舊金山--(美國商業資訊)--2024年3月4日-- Better Therapeutics 納斯達克股票代碼:BTTX)是開發用於治療心臟代謝疾病的處方數字療法(PDT)的先驅,今天宣佈接受了一份最新摘要,該摘要介紹了180天結果數據並參與了第17屆國際心臟代謝疾病會議 糖尿病的先進技術和治療 (ATTD),將於2024年3月6日至9日在意大利佛羅倫薩舉行。ATTD是展示糖尿病護理前沿進展的首要國際論壇,彙集了來自世界各地的臨床醫生、研究人員、行業領導者和政策制定者,交流知識並促進合作,尋求糖尿病管理的創新解決方案。

Key highlights of Better Therapeutics' participation at ATTD include:

Better Therapeutics參與ATTD的主要亮點包括:

Accepted 2024 ATTD Peer-Reviewed Abstract

2024 年 ATTD 同行評審摘要已接受

The late-breaking abstract findings further validate the use of AspyreRx as a safe and effective treatment for patients with type 2 diabetes (T2D). The abstract highlights statistically significant improvements in HbA1c, blood pressure, weight, mood, and quality of life in patients treated with AspyreRx compared to a Standard of Care control group at 180 days. AspyreRx patients also experienced significantly fewer adverse events and medication increases, thereby indicating meaningful reductions in overall healthcare utilization.

最新的摘要發現進一步證實了以下內容的使用 aspyerX 作爲2型糖尿病(T2D)患者的安全有效的治療方法。該摘要重點介紹了與標準護理對照組相比,接受AspyrerX治療的患者的HbA1c、血壓、體重、情緒和生活質量在180天時有統計學上的顯著改善。AspyrerX患者經歷的不良事件和藥物量增加的幅度也大大降低,這表明整體醫療利用率顯著下降。

Abstract Submission Number: 1282
Presentation Session: E-Poster Viewing
Abstract Title: Randomized, Controlled Trial Of A Novel Digital Therapeutic In Patients With Type 2 Diabetes: BT-001 Pivotal Trial 180 Day Outcomes

摘要提交編號: 1282
演示會議: 查看電子海報
摘要標題: 一種針對 2 型糖尿病患者的新型數字療法的隨機對照試驗:BT-001 關鍵試驗 180 天結果

Abstracts will be published in the peer-reviewed Journal of Diabetes Technology & Therapeutics.

摘要將發表在同行評審的《糖尿病技術與治療雜誌》上。

Industry Symposium

行業研討會

Additionally, Better Therapeutics will host a sponsored industry symposium on Saturday, March 09, 2024, at 8:30 a.m. local time (CET). Speaker Kara Mosesso, ANP-BC, CDCES, Medical Director at Better Therapeutics, will be joined by moderator David Rodbard, MD, Chief Scientific Officer at Biomedical Informatics Consultants. They will discuss the unmet treatment need in T2D, present AspyreRx's mechanism of action and pivotal data, and highlight the meaningfully enhanced efficacy of AspyreRx plus glucagon-like peptide 1 (GLP-1) agonist use compared to GLP-1 use without AspyreRx.

此外,Better Therapeutics將於當地時間2024年3月9日星期六上午8點30分(歐洲中部時間)舉辦贊助的行業研討會。揚聲器 卡拉·摩西索,主持人將加入Better Therapeutics醫學董事ANP-BC、CDCES的行列 大衛·羅德巴德,醫學博士,生物醫學信息學顧問公司首席科學官。他們將討論T2D中未得到滿足的治療需求,介紹AspyrerX的作用機制和關鍵數據,並重點介紹與不使用AspyrerX的 GLP-1 相比,使用AspyrerX加胰高血糖素樣肽1(GLP-1)激動劑的療效顯著提高。

Exhibition Booth

展覽攤位

Attendees will have the opportunity to experience AspyreRx firsthand and learn more about its clinical benefits at the Better Therapeutics exhibition booth. AspyreRx is the first and only U.S. Food and Drug Administration (FDA)-authorized fully digital lifestyle intervention designed to treat T2D.

與會者將有機會在Better Therapeutics展位上親身體驗AspyrerX並進一步了解其臨床益處。AspyrerX 是美國食品藥品監督管理局 (FDA) 批准的首款也是唯一一款專爲治療 T2D 而設計的完全數字化的生活方式干預措施。

"We are thrilled to participate in the prestigious ATTD Conference and share our latest research and insights with the global diabetes community," said Mark Berman, MD, Chief Medical Officer at Better Therapeutics. "We look forward to engaging with fellow experts, exchanging knowledge, and advancing the field of digital therapeutics to improve diabetes outcomes."

他說:“我們很高興參加久負盛名的ATTD會議,並與全球糖尿病界分享我們的最新研究和見解。” 馬克·伯曼,醫學博士,Better Therapeutics首席醫學官。“我們期待與其他專家互動,交流知識,推動數字療法領域的發展,以改善糖尿病的預後。”

For more information about ATTD 2024, visit: https://attd.kenes.com/

有關 ATTD 2024 的更多信息,請訪問: https://attd.kenes.com/

About Better Therapeutics

關於更好的療法

Better Therapeutics is a prescription digital therapeutics company developing a novel form of cognitive behavioral therapy to address underlying factors that sustain or worsen cardiometabolic diseases. The Company has developed a proprietary platform for the development of FDA-regulated, software-based solutions for T2D, heart disease and other conditions. The CBT delivered by Better Therapeutics' PDTs is designed to enable changes in neural pathways of the brain so lasting changes in behavior become possible. Addressing the underlying causes of these diseases has the potential to dramatically improve patient health while lowering healthcare costs. Better Therapeutics' clinically validated mobile applications are intended to be prescribed by physicians and reimbursed like traditional medicines.

Better Therapeutics是一家處方數字療法公司,正在開發一種新型的認知行爲療法,以解決維持或惡化心臟代謝疾病的潛在因素。該公司開發了一個專有平台,用於開發受美國食品藥品管理局監管的針對T2D、心臟病和其他疾病的基於軟件的解決方案。由Better Therapeutics的PDT提供的CBT旨在改變大腦的神經通路,從而使行爲的持久變化成爲可能。解決這些疾病的根本原因有可能顯著改善患者的健康,同時降低醫療成本。Better Therapeutics經過臨床驗證的移動應用程序旨在由醫生開處方,並像傳統藥物一樣報銷。

For more information visit: bettertx.com

欲了解更多信息,請訪問: bettertx.com

About AspyreRx

關於 AspyrerX

AspyreRx (formerly BT-001) was granted marketing authorization by the FDA in July 2023 as the first prescription-only digital therapeutic to treat adults with type 2 diabetes (T2D). AspyreRx is backed by robust data demonstrating clinically meaningful and sustained reduction in A1c as well as improvements in other markers of cardiometabolic health when used up to 180 days. Using proven techniques that target the underlying psychological, behavioral, and cognitive factors that sustain or worsen T2D, AspyreRx is a self-paced, engaging experience that patients can access from their smartphone. It is prescribed by a healthcare provider in 90-day increments, with proprietary CBT delivered digitally in a weekly step-by-step process. Through interactive therapy lessons, skill-building modules, weekly goal setting and tracking, patients connect changes in behavior to improvements in blood sugar and other biometrics. Each step in the experience builds on the prior to enable and reinforce cognitive restructuring, building the emotional resilience and acceptance needed to make enduring changes.

AspyrerX(前身爲 BT-001)於 2023 年 7 月獲得美國食品藥品管理局的上市許可,成爲第一款治療成人 2 型糖尿病 (T2D) 的僅限處方的數字療法。AspyrerX 有可靠的數據支持,這些數據表明,使用長達 180 天后,A1c 具有臨床意義的持續降低,心臟代謝健康的其他標誌物也會得到改善。AspyrerX 使用針對維持或惡化 T2D 的潛在心理、行爲和認知因素的成熟技術,提供一種自定進度、引人入勝的體驗,患者可以通過智能手機進行訪問。它由醫療保健提供者以 90 天爲增量開處方,專有的 CBT 每週分步以數字方式交付。通過互動治療課程、技能培養模塊、每週目標設定和跟蹤,患者將行爲的變化與血糖和其他生物識別技術的改善聯繫起來。體驗中的每一步都建立在先前的基礎上,以實現和強化認知重組,建立做出持久改變所需的情感適應力和接受能力。

Indications for Use

使用適應症

AspyreRx is a prescription-only digital therapeutic device intended to provide cognitive behavioral therapy to patients 18 years or older with type 2 diabetes. The device targets behavior to aid in the management of type 2 diabetes in patients who are under the care of a healthcare provider. AspyreRx provides cognitive behavioral therapy as a treatment that should be used adjunctively with standard of care.

AspyrerX 是一種僅限處方的數字治療設備,旨在爲 18 歲或以上的2型糖尿病患者提供認知行爲療法。該設備針對接受醫療保健提供者護理的患者的行爲,以幫助管理2型糖尿病。AspyrerX 提供認知行爲療法,作爲一種治療方法,應與標準護理一起使用。

Forward-Looking Statements

前瞻性陳述

Certain statements made in this press release are "forward-looking statements" within the meaning of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are typically identified by words such as "plan," "believe," "expect," "anticipate," "intend," "outlook," "estimate," "forecast," "project," "continue," "could," "may," "might," "possible," "potential," "predict," "should," "would" and other similar words and expressions, but the absence of these words does not mean that a statement is not forward-looking. The forward-looking statements in this press release include, but are not limited to, statements regarding Better Therapeutics' expectations related to the efficacy and potential benefits of PDTs, including AspyreRx, and CBT, and their potential treatment applications and their ability to improve clinical outcomes, expectations regarding the rebate agreement and the potential for the rebate agreement to increase accessibility and coverage of Better Therapeutics' products, and expectations regarding the commercial traction of AspyreRx and partnering and coverage discussions, among others. These forward-looking statements are based on the current expectations of the management of Better Therapeutics and are inherently subject to uncertainties and changes in circumstances and their potential effects and speak only as of the date of such statement. There can be no assurance that future developments will be those that have been anticipated. These forward-looking statements involve a number of risks, uncertainties or other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements including: risks related to Better Therapeutics' business, such as the willingness of the FDA to authorize PDTs for commercial distribution and insurance companies to reimburse their use, market acceptance of PDTs, including AspyreRx, the risk that the results of previously conducted studies will not be interpreted favorably by the FDA or repeated or observed in ongoing or future studies involving Better Therapeutics' product candidates and other risks and uncertainties included under the header "Risk Factors" in Better Therapeutics' quarterly report on Form-10-Q for the fiscal quarter ended September 30, 2023 filed with the Securities and Exchange Commission ("SEC") on November 09, 2023, and those that are included in any of the Company's subsequent filings with the SEC.

本新聞稿中的某些陳述是1995年《美國私人證券訴訟改革法》安全港條款所指的 “前瞻性陳述”。前瞻性陳述通常用 “計劃”、“相信”、“預期”、“打算”、“展望”、“估計”、“預測”、“項目”、“繼續”、“可能”、“可能”、“可能”、“可能”、“可能”、“潛在”、“預測”、“應該”、“將” 等詞語以及其他類似的詞語和表述來識別,但這些詞語的缺失不是意味着陳述不是前瞻性的。本新聞稿中的前瞻性陳述包括但不限於關於Better Therapeutics對包括AspyrerX和CBT在內的PDT的療效和潛在益處及其潛在治療應用及其改善臨床結果的能力的預期、對回扣協議和回扣協議可能性以增加Better Therapeutics產品可及性和覆蓋範圍的期望的陳述,以及對AspyrerX商業吸引力以及合作和承保範圍的期望討論等。這些前瞻性陳述基於Better Therapeutics管理層當前的預期,本質上受不確定性和情況變化及其潛在影響的影響,僅代表截至此類聲明發布之日。無法保證未來的發展會是預期的。這些前瞻性陳述涉及許多風險、不確定性或其他假設,可能導致實際結果或業績與這些前瞻性陳述所表達或暗示的結果存在重大差異,包括:與Better Therapeutics業務相關的風險,例如美國食品和藥物管理局是否願意批准PDT供商業分銷和保險公司報銷其使用費用,市場對包括AspyrerX在內的PDT的接受程度,以及先前進行的研究的結果得不到積極解釋的風險由在Better Therapeutics於2023年11月9日向美國證券交易委員會(“SEC”)提交的截至2023年9月30日的10-Q財季季度報告中,Better Therapeutics向美國證券交易委員會(“SEC”)提交的截至2023年9月30日的10-Q表季度報告中 “風險因素” 標題下包含的其他風險和不確定性以及公司隨後向美國證券交易委員會提交的任何文件中包含的風險和不確定性,或在正在進行或未來的研究中重複或觀察。

For media inquiries, please contact info@bettertx.com

媒體垂詢,請聯繫 info@bettertx.com

Source: Better Therapeutics, Inc.

來源:Better Therapeutics, Inc.

譯文內容由第三人軟體翻譯。


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