Science

Human genetic studies and functional mapping highlight the incretin axis as a key regulator of metabolic health. Loss-of-function variants in GIPR are associated with lower BMI and improved cardiometabolic traits, and GLP-1 receptor antagonists are proven to deliver clinically validated benefits in metabolic diseases.

GIPR mAb/GLP-1RA Fusion Protein

Alveus’ lead program—a GIPR antagonist/GLP-1 agonist Fusion Protein—is designed to harness the synergistic effects of these mechanisms to deliver durable, sustainable weight loss resulting in reduced treatment burden for patients.
Importantly, this dual approach aims to provide differentiated efficacy beyond current options by addressing counterregulatory metabolic mechanisms and improving long-term outcomes.

About the Alveus Pipeline

Lead Asset: ALV-100 Target Product Profile

Preclinical and Clinical Profile

Competitive in vitro potency and weight loss with lean mass preservation in obese NHPs. Weight loss and weight maintenance demonstrated in Ph1

Mechanism of Action

GIP receptor antagonism and GLP-1 receptor agonism

Molecular Design

Novel recombinant humanized GIPR antagonist IgG-4 antibody – GLP1 agonist peptide fusion protein

Dosing

Best-in-class dosing regimen

Indication

Weight Management

Our portfolio of novel therapeutics

At Alveus Therapeutics, we are developing a portfolio of novel therapeutics targeting metabolic diseases. Despite significant improvements in treatment options and market growth; substantial unmet needs persist, particularly in achieving sustained weight loss, as well as addressing the key underlying pathologies that impact cardiometabolic health outcomes.

We aim to address these critical issues, delivering meaningful and sustained improvements in patient outcomes. In addition to our lead program, we are advancing a robust pipeline of highly differentiated small molecules, peptides, and antibodies across multiple indications.

About the Alveus Pipeline

Building the Future of Medicine for Metabolic Disease