AustinPx, a contract development and manufacturing organization (CDMO) specializing in bioavailability enhancement of orally delivered small molecule drug candidates, and Microsize, a leading active pharmaceutical ingredient (API) enhancement CDMO, formed a partnership to accelerate the commercial application of AustinPx’s KinetiSol technology platform. The collaboration will enable AustinPx’s clients to manufacture their late-phase clinical and commercial KinetiSol drug product intermediate at Microsize’s purpose built, FDA-inspected facility.

KinetiSol is an innovative technology that utilizes frictional and shear energies to generate amorphous solid dispersions (ASD) in seconds, without the use of solvents. It has demonstrated higher exposure at lower doses with improved downstream processability compared to other ASD technologies. With its significantly smaller footprint, broader formulation design space for challenging molecules, and improved manufacturing economics, the KinetiSol platform is disrupting the ASD industry.

“AustinPx is excited to partner with Microsize, a like-minded client centric CDMO, on the commercial enablement of our KinetiSol Technology,” said Elizabeth Hickman, chief business officer, AustinPx. “Microsize provides our growing client base with an excellent, high-quality commercial partner for their late-phase and commercial KinetiSol production needs.”

As part of the agreement, AustinPx will transfer its proprietary KinetiSol equipment, software, and know-how to Microsize’s Quakertown facility. In turn, Microsize will install and qualify the equipment for late-phase and commercial manufacturing within their cGMP manufacturing plant. Microsize will provide staff for scale-up and commercial stage KinetiSol production, as well as associated capabilities including quality control and assurance. The KinetiSol Technology is projected to be available at Microsize for GMP production by the end of 2024.