MetaShape

SCIENCE

Activating the other side of the energy balance

ENERGY BALANCE

The Next Lever for GLP-1 Therapy

GLP-1 therapies help reduce energy intake by suppressing appetite. MS 001 is designed to complement that effect on the other side of the energy-balance equation: increasing fat-specific energy expenditure to support deeper, more durable, and muscle-sparing weight loss.

GLP-1 therapies help reduce energy intake by suppressing appetite. MS 001 is designed to complement that effect on the other side of the energy-balance equation: increasing fat-specific energy expenditure to support deeper, more durable, and muscle-sparing weight loss.

Up to 40%

of weight lost with GLP-1 receptor agonists consists of lean muscle mass.

Up to 65%

of patients discontinue GLP-1 agonists within 1 year due to side effects.

67%

of weight lost is regained within 1 year of stopping GLP-1 therapy (primarily as fat).

Up to 40%

of weight lost with GLP-1 receptor agonists consists of lean muscle mass.

Up to 65%

of patients discontinue GLP-1 agonists within 1 year due to side effects.

67%

of weight lost is regained within 1 year of stopping GLP-1 therapy (primarily as fat).

ABOUT MS 001

A GLP-1 Force Multiplier

MS 001 (ulodesine hemiglutarate) is a first-in-class, orally available small-molecule inhibitor of purine nucleoside phosphorylase (PNP), designed to amplify GLP-1 therapy effects by activating pathways that trigger fat-specific energy expenditure.
Enhances GLP-1 efficacy
Greater, fat-selective, muscle-sparing weight loss.
Reduces weight rebound
Following GLP-1 discontinuation.
Improves metabolic health
Supporting improved lipid and liver profile.

Clinical foundation
Human safety established
Ulodesine has been evaluated in more than 500 subjects and shown to be generally safe and well tolerated.

Novel Mechanism of Action
Novel Mechanism of Action

From PNP Inihibition to Fat-Tissue Energy Expenditure

MS 001 inhibits PNP and increases inosine and nicotinamide adenine dinucleotide (NAD+), key mediators associated with cellular energy metabolism, to support downstream energy-expenditure pathways in fat tissue via activation of futile calcium cycling and glucagon signaling pathways.
 MS 001 inhibits PNP and increases inosine and nicotinamide adenine dinucleotide (NAD+), key mediators associated with cellular energy metabolism, to support downstream energy-expenditure pathways in fat tissue via activation of futile calcium cycling and glucagon signaling pathways.
 Download the latest MetaShape presentation for more detail on MS 001’s mechanism, preclinical data, and development strategy.

Download the latest MetaShape presentation for more detail on MS 001’s mechanism, preclinical data, and development strategy.
Platform Potential

A Platform for Metabolic Amplification

As the metabolic health market expands, MS 001 has the potential to become a high-impact platform asset, opening opportunities in obesity, adjacent cardiometabolic indications, and possible future relevance in neuro-metabolic disease.
 As the metabolic health market expands, MS 001 has the potential to become a high-impact platform asset, opening opportunities in obesity, adjacent cardiometabolic indications, and possible future relevance in neuro-metabolic disease.
For investors and strategic partners, MS 001 is a force multiplier that can broaden GLP-1 utility and strengthen therapeutic differentiation.
 For investors and strategic partners, MS 001 is a force multiplier that can broaden GLP-1 utility and strengthen therapeutic differentiation.