Company to host sponsored education session on
Saturday, March 09, 2024; Expanding access to a high quality and
effective lifestyle modification intervention
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.
Key highlights of Better Therapeutics’ participation at ATTD
include:
Accepted 2024 ATTD Peer-Reviewed Abstract
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.
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
Abstracts will be published in the peer-reviewed Journal of
Diabetes Technology & Therapeutics.
Industry Symposium
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.
Exhibition Booth
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.
“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.”
For more information about ATTD 2024, visit:
https://attd.kenes.com/
About Better Therapeutics
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.
For more information visit: bettertx.com
About 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.
Indications for Use
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.
Forward-Looking Statements
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.
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