Simulations Plus and Enabling Technologies Consortium Announce Strategic Collaboration to Advance GastroPlus® Enhancements
22 Januar 2025 - 1:50PM
Business Wire
Industry partners to provide funding and
data to support ACAT™ model improvements
Simulations Plus, Inc. (Nasdaq: SLP) (“Simulations Plus”), a
leading provider of biosimulation, simulation-enabled performance
and intelligence solutions, and medical communications to the
biopharma industry, today announced that it has entered a new
funded collaboration with the Enabling Technologies Consortium
(ETC). This partnership is aimed at advancing in vitro-in vivo
correlation (IVIVC) approaches for oral drug delivery and expanding
the functionality of the GastroPlus platform.
The collaboration focuses on enhancing the predictive
capabilities of the GastroPlus advanced compartmental absorption
and transit (ACAT™) model to support the development of immediate
release (IR) oral drug products. Using data gathered from public
sources and members of the ETC, physiologically based
pharmacokinetics (PBPK) and biopharmaceutics modeling (PBBM)
experts and software engineers at Simulations Plus will look to
complete key objectives as defined by the partnership. These
advancements, including implementation of novel product-particle
size distribution (P-PSD) methodologies and enhanced food effect
modeling features, will provide researchers with powerful tools to
improve drug product development, reduce reliance on animal
studies, and streamline regulatory submissions.
“We are honored to collaborate with ETC, a consortium
representing leaders in pharmaceutical innovation who recognize the
critical role GastroPlus already plays in drug development,” said
Dr. Xavier Pepin, Vice President of PBPK R&D at Simulations
Plus and principal investigator for this project. “This partnership
reflects the trust and confidence the industry places in our
platform and the desire to support its continued evolution. By
advancing cutting-edge capabilities, we are not only reaffirming
our commitment to innovation but also empowering researchers to
solve complex biopharmaceutical challenges with even greater
precision and efficiency.”
The collaboration leverages the combined expertise of
Simulations Plus and ETC’s Participating Members, which include
leading pharmaceutical and biotechnology companies. Throughout the
project, Simulations Plus will deliver beta versions of the
enhanced GastroPlus platform to ETC members for testing. Upon
completion, the updated software will be accessible to the broader
user community. Consistent with all collaborations that Simulations
Plus enters, the Company will retain ownership of intellectual
property developed through this partnership, ensuring that future
enhancements to its platform continue to reflect Simulations Plus’
leadership in PBPK/PBBM science.
About the Enabling Technologies Consortium
The Enabling Technologies Consortium (ETC) serves as a dynamic
platform for pharmaceutical and biotechnology companies to exchange
ideas, share knowledge, and collaborate on pioneering new
technologies that enhance drug development and manufacturing
processes. With a mission centered on advancing pre-competitive
enabling technologies, ETC fosters partnerships between its member
companies and external collaborators. Pre-competitive initiatives
are defined as joint efforts among multiple pharmaceutical
organizations and third parties to develop tools, methodologies, or
refinements that drive efficiencies in drug development. These
outcomes are made widely accessible through publication, product
commercialization, or other dissemination methods.
By uniting industry leaders under a shared vision, ETC is
driving progress and empowering pharmaceutical companies to tackle
common challenges with innovative, enabling technologies. For more
information about ETC and its initiatives, please visit
https://www.etconsortium.org/.
About Simulations Plus, Inc.
With more than 25 years of experience serving clients globally,
Simulations Plus stands as a premier provider in the biopharma
sector, offering advanced software and consulting services that
enhance drug discovery, development, research, clinical trial
operations, regulatory submissions, and commercialization. Our
comprehensive biosimulation solutions integrate artificial
intelligence/machine learning (AI/ML), physiologically based
pharmacokinetics, physiologically based biopharmaceutics,
quantitative systems pharmacology/toxicology, and population PK/PD
modeling approaches. We also deliver simulation-enabled performance
and intelligence solutions alongside medical communications support
for clinical and commercial drug development. Our cutting-edge
technology is licensed and utilized by leading pharmaceutical,
biotechnology, and regulatory agencies worldwide. For more
information, visit our website at www.simulations-plus.com. Follow
us on LinkedIn | X | YouTube.
Environmental, Social, and Governance (ESG)
We focus our Environmental, Social, and Governance (ESG) efforts
where we can have the most positive impact. To learn more about our
latest initiatives and priorities, please visit our website to read
our 2023 ESG update.
Forward-Looking Statements
Except for historical information, the matters discussed in this
press release are forward-looking statements that involve risks and
uncertainties. Words like “believe,” “expect,” and “anticipate”
mean that these are our best estimates as of this writing, but
there can be no assurances that expected or anticipated results or
events will actually take place, so our actual future results could
differ significantly from those statements. Factors that could
cause or contribute to such differences include, but are not
limited to: our ability to successfully integrate the Pro-ficiency
business with our own, as well as expenses we may incur in
connection therewith, the efficiency and effectiveness of our
internal business restructuring and leadership changes, our ability
to maintain our competitive advantages, acceptance of new software
and improved versions of our existing software by our customers,
the general economics of the pharmaceutical industry, our ability
to finance growth, our ability to continue to attract and retain
highly qualified technical staff, market conditions, macroeconomic
factors, and a sustainable market. Further information on our risk
factors is contained in our quarterly and annual reports and filed
with the U.S. Securities and Exchange Commission.
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version on businesswire.com: https://www.businesswire.com/news/home/20250122083173/en/
Financial Profiles Lisa Fortuna
310-622-8251 slp@finprofiles.com Enabling
Technologies Secretariat James Vergis 202-230-5439
info@etconsortium.org
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