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
Obesity/Weight
Management
NPM-139*

Semaglutide

>$60B
Type 2 Diabetes
NPM-133

Semaglutide

>$60B
Obesity/Weight
Management
NPM-115

Exenatide

>$60B
Canine & Feline
Obesity
OKV-119***

Exenatide

>$2B
Indication
Obesity/Weight
Management
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-139*

Semaglutide

>$60B
Indication
Type 2 Diabetes
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-133

Semaglutide

>$60B
Indication
Obesity/Weight
Management
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-115

Exenatide

>$60B
Indication
Canine & Feline
Obesity
Feasibility
Pre-Clinical
Clinical
Market Size
OKV-119***

Exenatide

>$2B
Indication
Obesity/Weight
Management
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-139*

Semaglutide

>$60B
Indication
Type 2 Diabetes
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-133

Semaglutide

>$60B
Indication
Obesity/Weight
Management
Feasibility
Pre-Clinical
Clinical
Market Size
NPM-115

Exenatide

>$60B
Indication
Canine & Feline
Obesity
Feasibility
Pre-Clinical
Clinical
Market Size
OKV-119***

Exenatide

>$2B
*Feasibility recently established with semaglutide, supporting priority development.
**Estimated Market Sizes where Vivani products would compete, if approved. Does not represent future sales or revenue estimates of Vivani pipeline products.
TD Cowen estimates $139B in GLP-1 sales by 2030. We assume >$60B for Obesity/Chronic Weight Management and >$60B for Type 2 Diabetes by 2030.
***In Partnership with Okava Pharmaceuticals, Inc. Market size estimate based on Okava internal analysis.

NPM-139 (Semaglutide Implant): Our Lead Program

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

NPM-139, leveraging our NanoPortal™ technology, is designed to provide steady, long-term therapeutic delivery of semaglutide for at least six months.

By assuring medication adherence, NPM-139 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

A Successful First-in-Human Clinical Study of NanoPortal Technology.

LIBERATE-1, the First-in-Human Trial with our NanoPortal technology met all study objectives and paves the way for further advancement of our emerging, miniature drug implant portfolio. New preclinical data with a novel semaglutide implant showing ~ 20% weight loss with a single dose over six months supports priority advancement of the semaglutide implant toward clinical-stage development in 2026.

NPM-133 Overview

A miniature, GLP-1 receptor agonist implant designed for patients living with type 2 diabetes.

Built with our NanoPortal™ technology, NPM-133 is designed to provide steady, long-term therapeutic delivery of semaglutide for at least six months.

For patients with type 2 diabetes, the health risks associated with missed doses of prescribed medications can be severe. NPM-133, currently in development, offers the potential for these patients to receive the full therapeutic benefits of semaglutide treatment over six-months or more without interruption, providing convenience and peace-of-mind.

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.