Enabled by the proprietary Purcisiontechnology, LSAMs of pure drug are suspended at time of use and delivered directly to the disease site where the particles are retained as a depot continuously releasing drug molecules as the particles dissolve over time.
Large Surface Area Microparticles (LSAMs)
Intratumoral
Peritumoral
Intraperitoneal
Resection bed
Intravesicular
Instillation
Inhalation
Intracystic
Topical
Advantages
High sustained local concentration
Continuous tumor kill
Immunogenic effect
Gradual subtoxic clearance
Composition of matter patent on LSAMs protects particle regulatory specifications:
Size
Surface Area
Density
Dissolution
LSAMs are Superior to IV Drugs for Intratumoral Delivery
Taxane Solution for Injection Tumor Site
Paclitaxel or docetaxel injections are designed for IV administration and rapidly diffuse out of the tumor if injected intratumorally.
LSAM-PTX and LSAM-DTX are designed for local administration and become entrapped in the tumor allowing for high, continuous, local therapeutic drug release over time
Tumor tissue concentration of LSAM-PTX and LSAM-DTX versus comparators all given intratumorally in a mouse model
Proprietary PurcisionPlatform Large Surface Area Microparticle LSAM Production
API Crystals
Large and bulky crystals
Infeasible to form pharmaceutically acceptable particle suspension
Limited to dissolution in solvent as a solution for IV delivery
GMP full scale production suitable for clinical supplies and commercial launch
Uniquely uses supercritical fluid carbon dioxide as antisolvent to precipitate LSAMs
Platform technology for multiple drug classes including taxanes, platins, TKIs, PARPIs, others
LSAMs
100% pure drug with no excipients or coting agents
Right particle size for tumor retention
Increased surface area for high, continuous, local therapeutic drug release
Decreased bulk density for excellent suspension uniformity