Leveraging our NanoPortal™ technology, we are developing a portfolio of highly differentiated products comprised of miniature, sub-dermal drug implants.
high-dose exenatide
exenatide
semaglutide
exenatide
high-dose exenatide
exenatide
semaglutide
exenatide
high-dose exenatide
exenatide
semaglutide
exenatide
NPM-115, leveraging our NanoPortal™ technology, is designed to provide steady, long-term therapeutic delivery of high-dose exenatide for at least six months.
By assuring medication adherence, NPM-115 may free patients with obesity from burdens associated with oral and injectable medications, as well as provide confidence to physicians, caregivers and loved ones that patients are receiving the intended therapeutic benefits from their medicine.
Although the GLP-1 receptor agonist class has quickly outpaced previous anti-obesity medications due to superior efficacy and tolerability, medication non-adherence continues to affect an alarming number of patients – approximately 50%, including those taking daily pills. In fact, non-adherence may also contribute to the gap in real-world effectiveness compared to the efficacy reported from randomized, controlled, clinical trials.
In response to the unprecedented growth and focus on the anti-obesity and weight loss markets, we formally established NPM-115 and initiated feasibility studies with high-dose exenatide in our proprietary NanoPortal implant technology. Ongoing development work with NPM-119 and additional studies with high-dose exenatide should help accelerate further development activities of NPM-115.
Built with our NanoPortal™ technology, NPM-119 is designed to provide steady, long-term therapeutic delivery of exenatide for at least six months.
By assuring medication adherence, NPM-119 may free patients with type 2 diabetes from burdens associated with oral and injectable medications, as well as provide confidence to physicians, caregivers and loved ones that patients are receiving the intended therapeutic benefits from their medicine.
Medication non-adherence affects an alarming number of patients – approximately 50%
In 2023, we submitted an Investigational New Drug application with the U.S. FDA to support the initiation of a First-in-Human clinical study of NPM-119 called LIBERATE-1. In parallel, we plan to pursue the option of conducting studies in Australia, including LIBERATE-1, as well.
LIBERATE-1 is the first clinical study investigating the effects of NPM-119 in patients with type 2 diabetes and of our platform NanoPortal implant technology.