{"id":953223,"date":"2026-04-21T07:58:06","date_gmt":"2026-04-21T11:58:06","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/"},"modified":"2026-04-21T07:58:06","modified_gmt":"2026-04-21T11:58:06","slug":"simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/","title":{"rendered":"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products"},"content":{"rendered":"<p>        <!--.bwalignc { text-align: center; list-style-position: inside }body {font:normal small Arial,Helvetica,sans-serif;color:#000;background-color:#fff;padding:24px;margin:0;} a img {border:0;} h3 {font-size:medium;color:#000;margin:0 0 1em 0; text-align:center;}-->  <\/p>\n<p class=\"bwalignc\"><b>Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products<\/b><\/p>\n<p class=\"bwalignc\"><i>Mechanistic modeling approach and experimental integration designed to improve early risk identification, strengthen regulatory confidence, and expand AI-enabled workflows connecting data to decision-making<\/i><\/p>\n<p>RESEARCH TRIANGLE PARK, N.C.&#8211;(<a href=\"http:\/\/www.businesswire.com\">BUSINESS WIRE<\/a>)&#8211;<br \/>\nSimulations Plus, Inc. (Nasdaq: SLP) (\u201cSimulations Plus\u201d or the \u201cCompany\u201d), a global leader in model-informed and AI-accelerated drug development that advances biopharma innovation, today announced a funded research collaboration with Lonza Group AG (\u201cLonza\u201d), a leading contract development and manufacturing organization (CDMO) dedicated to serving the healthcare industry, and the U.S. Food and Drug Administration (FDA) to develop and validate a mechanistic, predictive framework for assessing the <i>in vivo<\/i> performance of amorphous solid dispersion (ASD) drug products.<\/p>\n<p>\n\u201cComplex oral formulations such as amorphous solid dispersions present significant scientific and regulatory challenges due to their sensitivity to physiological and manufacturing variables,\u201d said Dr. Viera Lukacova, Chief Scientific Officer of Simulations Plus. \u201cThrough this funded collaboration, we aim to integrate advanced <i>in vitro<\/i> systems with mechanistic modeling to improve prediction of <i>in vivo<\/i> performance, support regulatory decision-making, and enable more efficient development pathways for these high-impact therapies that deliver faster dissolution and more drug absorption.\u201d<\/p>\n<p><b>Advancing Mechanistic, Model-Informed Approaches for Complex Products<\/b><\/p>\n<p>\nASDs are among the most powerful yet complex oral drug delivery systems, with performance influenced by factors such as food intake, gastric pH, formulation composition, and manufacturing processes. Current regulatory approaches often require multiple clinical bioequivalence (BE) studies, which can be resource-intensive while still carrying uncertainty.<\/p>\n<p>\nThe collaboration evaluates whether advanced <i>in vitro<\/i> dissolution systems\u2014particularly those incorporating dynamic gastrointestinal physiology\u2014combined with mechanistic physiologically based biopharmaceutics modeling (PBBM), can reliably predict key <i>in vivo<\/i> outcomes, including food effects and the impact of elevated gastric pH conditions.<\/p>\n<p>\nBy establishing and validating these predictive capabilities, the collaboration aims to provide a scientific foundation for reducing reliance on certain clinical BE studies while maintaining the rigor and transparency required by regulators.<\/p>\n<p><b>Integrating Experimental and Mechanistic Modeling Expertise<\/b><\/p>\n<p>\nThe collaboration brings together complementary capabilities across experimental science and computational modeling.<\/p>\n<p>\nLonza will lead experimental work, including <i>in vitro<\/i> dissolution testing under fasted, fed, and elevated gastric pH conditions using advanced systems such as Controlled Transfer Dissolution (CTD), as well as the characterization and, where needed, manufacturing of ASD formulation variants.<\/p>\n<p>\nSimulations Plus will lead the development and validation of <i>in vitro\u2013in vivo<\/i> extrapolation (IVIVE) frameworks using its DDDPlus\u00ae and GastroPlus\u00ae platforms, translating experimental data into predictions of <i>in vivo<\/i> pharmacokinetics and supporting virtual bioequivalence assessments. At the same time, it creates new opportunities to extend these capabilities into grounded AI-enabled workflow environments, where data, mechanistic models, and simulation outputs will be more directly connected. The Company will also contribute to interpretation within a regulatory context, ensuring alignment with evolving expectations for model-informed drug development (MIDD).<\/p>\n<p>\nFrancois Ricard, Head of R&amp;D, Lonza Advanced Synthesis, said, \u201cThis collaboration reflects Lonza\u2019s commitment to advancing more predictive, science-driven approaches as the leader in the field of bioavailability enhancement. By combining advanced <i>in vitro<\/i> experimentation with mechanistic modeling, and working closely with Simulations Plus and the FDA, we aim to strengthen the scientific foundation that underpins regulatory decision-making for complex oral drug products. Ultimately, this type of collaboration should help accelerate development for our customers requiring bioequivalence during clinical development.\u201d<\/p>\n<p><b>Alignment with Regulatory Priorities and Industry Needs<\/b><\/p>\n<p>\nThis work is supported in part through FDA funding and includes ongoing engagement with FDA scientists to directly align with regulatory priorities to advance MIDD, modernize bioequivalence assessment for complex products, and reduce unnecessary reliance on human studies. By combining regulatory collaboration with open, non-proprietary data and validated methods based on real-world, FDA-approved ASD products, the initiative is intended to inform future regulatory approaches and support broader adoption of science-based alternatives.<\/p>\n<p>\n\u201cThe industry is moving toward a future where decisions are informed earlier, with greater confidence and scientific transparency,\u201d added Lukacova. \u201cOur role is to ensure those decisions are grounded in validated science\u2014while enabling more efficient ways to connect data, models, and insight.\u201d<\/p>\n<p><b>About Simulations Plus, Inc.<\/b><\/p>\n<p>\nSimulations Plus is a global leader in model-informed and AI-accelerated drug development. We create value for our clients by accelerating the discovery, development, and commercialization of pharmaceuticals and other products through innovative science-based software and consulting solutions. For more information, visit <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fnam12.safelinks.protection.outlook.com%2F%3Furl%3Dhttp%253A%252F%252Fwww.simulations-plus.com%252F%26data%3D05%257C02%257Cchristina.hendrickson%2540simulations-plus.com%257Ce00a5e418fc14363254b08de337406c4%257Ca6fe9a739e054efcb9b3f4cc5eab196c%257C0%257C0%257C639004771726597036%257CUnknown%257CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%253D%253D%257C0%257C%257C%257C%26sdata%3DVl%252BNsGSLmZtDcsrlp0M1V9NI3JD3jT5%252BD3bn1M3Ffn8%253D%26reserved%3D0&amp;esheet=54517668&amp;newsitemid=20260421564555&amp;lan=en-US&amp;anchor=www.simulations-plus.com&amp;index=1&amp;md5=6ed6f28aa1ea3f2eef0a7eacb6e23ad9\">www.simulations-plus.com<\/a>.<\/p>\n<p><b>Forward-Looking Statements<\/b><\/p>\n<p>\nExcept for historical information, the matters discussed in this press release are forward-looking statements that involve risks and uncertainties. Words like \u201cbelieve,\u201d \u201cwill\u201d, \u201ccan\u201d, \u201cexpect,\u201d \u201canticipate,\u201d and similar expressions (or the negative of such terms, as well as other words or expressions referencing future events, conditions, or circumstances) 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. Forward-looking statements include but are not limited to statements regarding our fiscal year 2026 guidance, revenue growth, anticipated margins and profitability, demand to software and services, the impact of pricing actions, client spending levels, market conditions, the development, capabilities, regulatory acceptance, regulatory compliance and commercialization of AI-enabled and could-based solutions, the timing and content of product initiatives discussed at Investor Day, and our ability to execute our long-term strategic vision. These forward-looking statements are based on current assumptions and expectations that involve risks and uncertainties that could cause the actual results to differ materially from those expressed or implied. Factors that could cause or contribute to such differences include, but are not limited to: effectiveness of our internal operational structure, our ability to maintain our competitive advantages and commercialize AI and cloud-enabled solutions, evolving regulatory and data privacy standards governing AI technologies, 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, annual, and current reports and filed with the U.S. Securities and Exchange Commission. No regulatory authority has endorsed, approved, or validated the Company\u2019s products, platforms, or AI-related approaches.<\/p>\n<p><img decoding=\"async\" alt=\"\" src=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20260421564555r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\" style=\"width:0;height:0\" \/><span class=\"bwct31415\" \/><\/p>\n<p id=\"mmgallerylink\"><span id=\"mmgallerylink-phrase\">View source version on businesswire.com: <\/span><span id=\"mmgallerylink-link\"><a href=\"https:\/\/www.businesswire.com\/news\/home\/20260421564555\/en\/\" rel=\"nofollow\">https:\/\/www.businesswire.com\/news\/home\/20260421564555\/en\/<\/a><\/span><\/p>\n<p><b>Investor Relations Contact<\/b>:<br \/>\n<br \/>Lisa Fortuna<br \/>\n<br \/>Financial Profiles<br \/>\n<br \/>310-622-8251<br \/>\n<br \/><a rel=\"nofollow\" href=\"mailto:slp@finprofiles.com\">slp@finprofiles.com<\/a><\/p>\n<p><b>KEYWORDS:<\/b> North Carolina United States North America<\/p>\n<p><b>INDUSTRY KEYWORDS:<\/b> Software Research Professional Services Pharmaceutical Technology Artificial Intelligence Science Biotechnology FDA Consulting Other Science Health<\/p>\n<p><b>MEDIA:<\/b><\/p>\n<table cellpadding=\"3\" cellspacing=\"3\">\n<tr>\n<td><font face=\"Arial\" size=\"2\"><b>Logo<\/b><\/font><\/td>\n<\/tr>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20260421564555\/en\/1534621\/3\/SLP-Logo-Stacked.jpg\" alt=\"Logo\" \/><\/td>\n<\/tr>\n<tr>\n<td><font face=\"Arial\" size=\"2\"><\/font><\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"<p>Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products Mechanistic modeling approach and experimental integration designed to improve early risk identification, strengthen regulatory confidence, and expand AI-enabled workflows connecting data to decision-making RESEARCH TRIANGLE PARK, N.C.&#8211;(BUSINESS WIRE)&#8211; Simulations Plus, Inc. (Nasdaq: SLP) (\u201cSimulations Plus\u201d or the \u201cCompany\u201d), a global leader in model-informed and AI-accelerated drug development that advances biopharma innovation, today announced a funded research collaboration with Lonza Group AG (\u201cLonza\u201d), a leading contract development and manufacturing organization (CDMO) dedicated to serving the healthcare industry, and the U.S. Food and Drug Administration (FDA) to develop and validate a mechanistic, predictive framework for assessing the in vivo performance of amorphous solid dispersion &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-953223","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products Mechanistic modeling approach and experimental integration designed to improve early risk identification, strengthen regulatory confidence, and expand AI-enabled workflows connecting data to decision-making RESEARCH TRIANGLE PARK, N.C.&#8211;(BUSINESS WIRE)&#8211; Simulations Plus, Inc. (Nasdaq: SLP) (\u201cSimulations Plus\u201d or the \u201cCompany\u201d), a global leader in model-informed and AI-accelerated drug development that advances biopharma innovation, today announced a funded research collaboration with Lonza Group AG (\u201cLonza\u201d), a leading contract development and manufacturing organization (CDMO) dedicated to serving the healthcare industry, and the U.S. Food and Drug Administration (FDA) to develop and validate a mechanistic, predictive framework for assessing the in vivo performance of amorphous solid dispersion &hellip; Continue reading &quot;Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-04-21T11:58:06+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20260421564555r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products\",\"datePublished\":\"2026-04-21T11:58:06+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\\\/\"},\"wordCount\":1114,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/cts.businesswire.com\\\/ct\\\/CT?id=bwnews&amp;sty=20260421564555r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\\\/\",\"name\":\"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products - 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(Nasdaq: SLP) (\u201cSimulations Plus\u201d or the \u201cCompany\u201d), a global leader in model-informed and AI-accelerated drug development that advances biopharma innovation, today announced a funded research collaboration with Lonza Group AG (\u201cLonza\u201d), a leading contract development and manufacturing organization (CDMO) dedicated to serving the healthcare industry, and the U.S. Food and Drug Administration (FDA) to develop and validate a mechanistic, predictive framework for assessing the in vivo performance of amorphous solid dispersion &hellip; Continue reading \"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/","og_site_name":"Market Newsdesk","article_published_time":"2026-04-21T11:58:06+00:00","og_image":[{"url":"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20260421564555r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"5 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products","datePublished":"2026-04-21T11:58:06+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/"},"wordCount":1114,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/#primaryimage"},"thumbnailUrl":"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20260421564555r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/simulations-plus-announces-collaboration-with-lonza-and-u-s-fda-to-advance-predictive-frameworks-for-complex-oral-drug-products\/","name":"Simulations Plus Announces Collaboration with Lonza and U.S. FDA to Advance Predictive Frameworks for Complex Oral Drug Products - 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