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Simulations Plus Receives New Grant Award From the FDA
Rhea-AI Impact
(Moderate)
Rhea-AI Sentiment
(Very Positive)
Tags
Rhea-AI Summary
Simulations Plus has received a cooperative agreement from the FDA, providing $250,000 annually for two years to enhance its GastroPlus® platform. This funding aims to improve the Transdermal Compartmental Absorption and Transit (TCAT™) model for better simulations of dermal formulations. The project will involve collaboration with leading pharmaceutical and research organizations, focusing on developing innovative strategies for regulatory assessments. This initiative strengthens the company's position in drug modeling and simulation, particularly in dermatology.
Positive
Awarded a cooperative agreement with the FDA for $250,000 per year for up to two years.
Enhancements to the GastroPlus® platform are expected to improve accuracy in regulatory assessments for dermal products.
Collaborative project with leading pharmaceutical and research organizations enhancing industry relationships.
Potential to cement GastroPlus as a leading modeling platform for dermal absorption and pharmacokinetics.
Negative
None.
Improvements to the GastroPlus® platform will increase its impact in driving research and regulatory decisions on dermatological products
LANCASTER, Calif.--(BUSINESS WIRE)--
Simulations Plus, Inc. (Nasdaq: SLP), a leading provider of modeling and simulation solutions for the pharmaceutical, biotechnology, chemical, and consumer goods industries, today announced that it has received notice from the U.S. Food and Drug Administration (FDA) that it has been awarded a new funded cooperative agreement, for $250,000 per year for up to two years, to further enhance the predictive power of the mechanistic Transdermal Compartmental Absorption and Transit (TCAT™) model in GastroPlus® in support of regulatory interactions.
Dr. Viera Lukacova, Chief Scientist at Simulations Plus, said: “We have been engaged with various groups at the FDA since 2014 on numerous funded research programs focused on physiologically based pharmacokinetic (PBPK) modeling of complex generics and non-oral administration routes. We are delighted to have earned the FDA’s confidence to broaden our relationship with another project through a competitive bidding process. This grant award has several major aims, including the expansion of dermal formulations which can be mechanistically simulated via the TCAT model within GastroPlus, implementation of new virtual population groups, and extension of bioequivalence calculations to account for local skin concentrations. These advancements will enable researchers and regulatory scientists to more quickly, and easily, simulate countless scenarios with improved accuracy, leading to updated scientific and regulatory standards for supporting innovative development and bioequivalence assessments for dermatological products.”
Under the cooperative agreement, FDA and Simulations Plus scientific and program staff will actively assist and participate in project activities in a partnership role with several leading pharmaceutical, generic, consumer goods, and contract research organizations. Drs. Jessica Spires and Manas Shah, Senior Scientists II at Simulations Plus, will serve as principal investigators and have primary responsibility for the scientific, technical, and programmatic aspects of the award and day-to-day management of the project.
“The TCAT model in GastroPlus is being utilized today by an ever-growing number of companies and academic centers worldwide to support product development and risk assessment activities,” added John DiBella, Simulations Plus Division President. “This new award, and the access to novel data which comes with it, will allow us to develop and validate innovative in vitro-in vivo strategies and further cement GastroPlus as the preeminent dermal absorption/PBPK modeling platform. Simulations Plus will own all intellectual property developed within the GastroPlus program, and updates will be integrated into future versions of the optional dermal module. As always, we continue to invite future collaborations to drive advances to modeling and simulation science which benefit our entire user community and, most importantly, the patients that we serve.”
Funding for this collaboration is made possible by the Food and Drug Administration through grant 1U01FD007320-01. Views expressed in this press release do not necessarily reflect the official policies of the Department of Health and Human Services; nor does any mention of trade names, commercial practices, or organization imply endorsement by the United States Government.
About Simulations Plus, Inc.
Serving clients worldwide for 25 years, Simulations Plus, Inc., is a leading provider of modeling and simulation software and consulting services supporting drug discovery, development research, and regulatory submissions. With our subsidiaries Cognigen, DILIsym Services, and Lixoft, we offer solutions that bridge machine learning, physiologically based pharmacokinetics, quantitative systems pharmacology/toxicology, and population PK/PD modeling approaches. Our technology is licensed and applied by major pharmaceutical, biotechnology, chemical, consumer goods companies, and regulatory agencies worldwide. For more information, visit our website at www.simulations-plus.com. Follow us on Twitter | Read our Environmental, Social, and Governance (ESG) Report.
Safe Harbor Statement Under the Private Securities Litigation Reform Act of 1995 – With the exception of historical information, the matters discussed in this press release are forward-looking statements that involve a number of risks and uncertainties. Words like “believe,” “expect” and “anticipate” mean that these are our best estimates as of this writing, but that 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 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, our ability to identify and close acquisitions on terms favorable to the Company, 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.
