AdipoPharma
company
We are developing PATAS, a unique first-in-class insulin sensitizer that targets the adipocyte and that will treat insulin resistance, type 2 diabetes and associated comorbidities.
Targeted Innovation
PATAS Peptide
Clinical Expertise
Metabolic Balance
What is AdipoPharma?
We are a French biotech company committed to understanding the role of the adipocyte cells in diabetes via their unique effect on lipid biosynthesis and management of whole-body lipid homeostasis.
The company was created to commercialize the work of its founder, Dr. Vincent Marion PhD, MSc, and Biochemist and researcher at INSERM, the French National Institute for Health and Medical Research. Dr Marion’s team has spent more than a decade identifying therapeutic targets based on the adipocyte’s specific role in the metabolic effects of insulin resistance and diabetes.
This work began by the detailed genetic investigation of Alström syndrome, an ultra-rare devastating disease characterized by severe insulin resistance, early-onset type 2 diabetes and associated metabolic dysfunctions.
This led to the development of a detailed analysis of the adipocyte’s complex function, its intrinsic lipid modulating effects and a proprietary targeted approach to treatment.
The result is AdipoPharma’s innovative and first-in-class therapeutic peptide “PATAS”, which enter clinical trial phase in 2025. This safe and novel therapeutic approach has been shown to restore healthy lipid biosynthesis in the diseased adipocyte leading to reduction of unhealthy lipids like the ceramides. PATAS is set to be the first anti-diabetic drug to have a significant beneficial effect on insulin resistance, beta cell plaque removal, liver steatosis and fibrosis and ceramides, the leading cause of cardiovascular dysfunction in diabetes.
Our Science
Inspired by genetic-derived knowledge to design innovative metabolic drugs targeting the adipocyte
Redefining Diabetes Treatment
AdipoPharma is pioneering a new class of metabolic therapy using stapled peptides designed to restore the natural function of adipocytes, the fat cells at the heart of metabolic regulation.
By specifically targeting insulin resistance, our lead therapeutic, PATAS, addresses the root cause of type 2 diabetes rather than just managing symptoms.
This innovative approach aims to reduce toxic lipids like ceramides, improve liver health, and support pancreatic β-cell function, offering new hope for millions affected by this chronic disease.


PATAS
a macrocyclic molecule
A first-in-class stapled peptide to target type 2 diabetes at its root cause.
PATAS is AdipoPharma’s breakthrough peptide drug designed to restore metabolic health by acting directly on the adipose tissue. Pre-clinical results show it improves glucose absorption, reduces insulin resistance, and tackles complications like liver fibrosis and cardiovascular issues.
Team Members

James Michael Nolan

John H. Friedman

Alan Cherrington

Guy Heynen

Vincent Marion

Vincent Marion
Founder, President & CEO

Catherine Perot
Chief Financial Officer

Michael J. Fare
Chief Operating Officer

Tarekegn G. Hiwot
Chief Medical Officer

Virginie Barthel
Director of Clinical Operations

Martine Brandt
Office Manager

Ralph Defronzo

Bob Seevers

Kenneth Draper

Bruno Kieffer

Alan Cherrington

Alexander Fleming

Paul Zimmet
scientific publications and communications

Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation
- Pnas
- 106(6)
- 1820-1825

BBS-Induced Ciliary Defect Enhances Adipogenesis, Causing Paradoxical Higher-Insulin Sensitivity, Glucose Usage, and Decreased Inflammatory Response
- Cell Metabolism
- Volume 16, Issue 3
- 363-377

147-LB: PATAS, an Adipocyte-Targeted Peptide Approach to Treat Type 2 Diabetes and Associated Comorbidities
- Diabetes
- 68(Supplement_1)
- 147-LB

Relative Adipose Tissue Failure in Alström Syndrome Drives Obesity-Induced Insulin Resistance
- Diabetes
- 70(2)
- 364–376

PATAS, a First-in-Class Therapeutic Peptide Biologic, Improves Whole-Body Insulin Resistance and Associated Comorbidities In Vivo
- Diabetes
- 71(9)
- 2034–2047