Revolutionizing the treatment of chronic disease.

Leveraging our NanoPortal technology, we are developing a portfolio of highly differentiated products comprised of miniature, sub-dermal drug implants.

Our Pipeline

Indication
Feasibility
Pre-Clinical
Clinical
Market Size
Human Obesity
NPM-115

high-dose exenatide

>$50B
Human Type II Diabetes
NPM-119

exenatide

>$20B
Human Obesity
NPM-139

semaglutide

>$50B
Feline Pre-Diabetes & Diabetes
OKV-119**

exenatide

>$0.5B
Indication
Human Obesity
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-115

high-dose exenatide

>$50B
Indication
Human Type II Diabetes
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-119

exenatide

>$20B
Indication
Human Obesity
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-139

semaglutide

>$50B
Indication
Feline Pre-Diabetes & Diabetes
Feasibility
Pre-Clinical
Clinical
Market Size
OKV-119**

exenatide

>$0.5B
Indication
Human Obesity
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-115

high-dose exenatide

>$50B
Indication
Human Type II Diabetes
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-119

exenatide

>$20B
Indication
Human Obesity
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-139

semaglutide

>$50B
Indication
Feline Pre-Diabetes & Diabetes
Feasibility
Pre-Clinical
Clinical
Market Size
OKV-119**

exenatide

>$0.5B

NPM-115 Overview

A miniature, GLP-1 receptor agonist implant designed to address medication non-adherence and improve tolerability.

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.

Target

Under investigation for chronic weight management/obesity.

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.

Development

First-in-Human clinical trial.

Pending regulatory clearance, we plan to initiate a First-in-Human clinical study supporting NPM-115 called LIBERATE-1 in Australia.

LIBERATE-1 is the first clinical study investigating the effects of our GLP-1 implant in obese or overweight individuals and the first clinical study utilizing of our platform NanoPortal implant technology.

NPM-119 Overview

A miniature, GLP-1 receptor agonist implant designed to address medication non-adherence and improve tolerability.

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.

Target

Under investigation for the treatment of type 2 diabetes.

Medication non-adherence affects an alarming number of patients – approximately 50%, including those taking daily pills. Non-adherence may contribute to the gap in real-world effectiveness compared to the efficacy reported from randomized, controlled, clinical trials.

Development

Portfolio Synergies.

In addition to providing support for NPM-115, our lead program in weight management, the LIBERATE-1 trial will also provide key insight for the NPM-119 program by including a Bydureon (exenatide injection) arm enabling pharmacokinetic comparison of exenatide concentrations between the exenatide implant and the marketed product. This information will help assess the translation of exenatide delivery in animal models to exenatide delivery in humans.