Simcyp Biopharmaceutics helps drug developers replace costly clinical bioequivalence studies and optimize formulations for complex therapies
Princeton, NJ – November 21st, 2023 – Certara, Inc. バイオシミュレーションのグローバルリーダーであるサターラ（Nasdaq：CERT) はCERT), a global leader in biosimulation, today announced the introduction of Simcyp™ Biopharmaceutics software. It is designed for use by biopharmaceutic, formulation, and CMC scientists to aid in formulating complex novel and generic small molecule medicines quickly and cost effectively. Simcyp Biopharmaceutics software is part of the Simcyp Simulator biosimulation platform, which has supported label claims for more than 100 approved novel therapies.
“The Simcyp Simulator is well recognized for its applications in clinical development, including prediction of drug-drug interactions, drug-food interactions, and drug performance in populations such as pediatrics and organ impairment,” said Rob Aspbury, President of Certara Scientific Software. “To further meet client requests and regulatory needs in earlier stages of drug development, we have been investing in advanced scientific formulation modeling technology and participating in US FDA R&D grant programs in this area for the past five years.”
Simcyp Biopharmaceutics software also helps sponsors develop the evidence needed to attain biowaivers which are used in lieu of conducting clinical studies. It is available as a standalone product and is designed for life sciences companies of all sizes looking to optimize their therapies’ formulations to maximize safety, efficacy, and patient convenience.
Simcyp Biopharmaceutics software delivers value and unique capabilities across several areas that are critical to achieving formulation success, including:
- Replace Costly Clinical Bioequivalence Studies – With growing encouragement from regulators, virtual bioequivalence studies (VBE) leverages physiologically based pharmacokinetic (PBPK) modeling to demonstrate bioequivalence (BE) between test and reference drugs. Simcyp Biopharmaceutics software includes a VBE module that automates elements of trial design significantly enhancing opportunities for attaining biowaivers.
- Optimize Formulation for Complex Drugs: Biopharmaceutical Classification System (BCS) Class II-IV drugs are challenging to create oral formulations for because of their poor solubility and/or absorption. Simcyp Biopharmaceutics software facilitates developing these drugs, which constitute 90% of new drug candidates.
- Inform Drug Labels – Recent FDA guidance recognizes physiologically-based pharmacokinetic (PBPK) models as a valuable technology for identifying and optimizing the impact of gastrointestinal effects such as meal type and pH. Simcyp Biopharmaceutics software advances these capabilities for optimizing dosing strategies and providing label guidance to clinicians.
For more information about Simcyp Biopharmaceutics software, please visit our website.
Certara（サターラ）について
サターラは、バイオシミュレーションソフトウェア、技術、サービスを用いて医薬品を加速し、従来の創薬・医薬品開発を変革します。製薬、教育機関、規制当局のお客様 2,300人以上、7062ヵ国にてサターラの技術やサービスが活用されています。詳細は弊社ホームページをご覧ください。
お問合せ先
Sheila Rocchio
sheila.rocchio@certara.com
報道機関の皆様：
赤津 笑美
emi.akatsu@certara.com
ariane.lovell@finnpartners.com
投資家の皆様：
David Deuchler
Gilmartin Group
ir@certara.com
