Catalent Launches New OptiDose® Design Solution to Help Create Differentiated Treatments that are Successful for Innovators, Patients and Health Care Professionals
Catalent today announced the launch of its new OptiDose® Design Solution, a comprehensive assessment of your molecule, patient, and market. Designed to incorporate recommendations from our scientific advisors to help drive the dose design decision-making process and create successful treatments.
SOMERSET, N.J. – July 26, 2021 — Catalent, the leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, cell and gene therapies, and consumer health products, today announced the launch of its new OptiDose® Design Solution, at the Controlled Release Society (CRS) annual meeting, which is taking place virtually from July 25 – 29, 2021.
Catalent’s OptiDose Design Solution, led by Catalent’s scientific advisors, uses a design approach that combines data-driven scientific tools with Catalent’s extensive development expertise. Integrating pharmaceutics, and dose form design target patient characteristics, OptiDose Design Solution will help craft the ideal dose form for all stakeholders and optimize the potential of a molecule.
“Taking patient needs and market realities into consideration earlier in the drug development process, along with critical CMC and DMPK parameters, is vital for creating a successful treatment for patients, innovators and health care professionals alike,” commented Julien Meissonnier, Chief Scientific Officer at Catalent. He continued, “The OptiDose Design platform looks to evaluate all these considerations and provide options for final dose form decisions with an optimal combination of patient acceptance and adherence, differentiation versus any standard of care, manufacturability and cost.”
At the CRS meeting, Lisa Caralli, Director of Science and Technology at Catalent, will discuss the methodology of the OptiDose Design Solution, including how key product and patient factors are evaluated. Ms. Caralli’s presentation, titled “Strategies to Optimize the Dose Design Process to Create Better Treatments”, will use case studies to demonstrate how the correct guidance, at the optimum time, can help drug developers create better treatments.
Ms. Caralli has over 27 years of industry experience, and in her role at Catalent, works with pharmaceutical companies to identify appropriate development pathways for early development drug candidates. She has previously held roles at Ionis Pharmaceuticals and Amylin Pharmaceuticals and began her career at the Immune Response Corporation. Ms. Caralli holds a bachelor’s degree in biochemistry from the University of California at Davis, California.
OptiDose Design Solution is available throughout Catalent’s global oral dose network. For more information, please visit https://www.catalent.com/oral-dose/dose-form-design/optidose-design-solution.
