Protego

At the forefront of drug discovery
targeting protein misfolding diseases

At the forefront of drug discovery
targeting protein misfolding diseases

We are laser focused on accelerating the development of first-in-class therapies for protein misfolding diseases, which represent a critical challenge in medical research due to their intricate mechanisms and the current lack of effective treatments.

Target Selection

High-Confidence Targets, Data Driven Analysis

We use monogenic or pathway genetic evidence, bioinformatics, deep biology, and clinical pathology analysis to target unmet medical needs.

Drug Discovery

Disease Modifying Focus, Innovative Discovery Platform

Developing pharmacological chaperones to directly bind to and modulate target protein stability to restore healthy-state structure and function.

Translational Research

Biomarker Discovery, Precision Medicine

Specific and sensitive biomarkers will enable early patient identification and provide clinical stage readouts for target engagement and therapeutic efficacy.

About Us

Protego focuses on the discovery and development of first-in-class small-molecule therapeutics that aim to reprogram protein folding for the treatment of various diseases.

We are exploring monogenetic protein misfolding diseases that cause myopathy, cardiomyopathy, stroke, renal disease, retinal diseases, channelopathies, and various degenerative diseases.

Our approach builds on the proven pharmacological chaperones approach previously exemplified by tafamidis, which was discovered and developed by our cofounders Dr. Jeffery W. Kelly and Dr. Richard Labaudinière, for the treatment of transthyretin amyloidosis.

Our Team

Leadership

Board of Directors

Shelley Chu, M.D., Ph.D.

Scientific Advisory Board

Investors

Our Science

Proteins are the molecular engines of human biology, responsible for a wide range of essential physiological processes. The structural integrity of proteins is critical to their biological functions, and disruptions in this integrity—known as protein misfolding—are increasingly recognized as the root cause of many chronic degenerative diseases. Protein misfolding can result in two major outcomes: 1) the loss of normal biological function, and 2) the acquisition of harmful, toxic functions.

Protein homeostasis, or proteostasis, is governed by a delicate balance of protein folding, misfolding, and aggregation dynamics. This balance is further modulated by a network of tightly regulated biological pathways that manage protein synthesis, folding, trafficking, and degradation both inside and outside of cells.

Protego BioPharma addresses the challenges of protein misfolding by targeting the energetics of protein folding and stability through small molecule interactions, such as pharmacological chaperones. Additionally, we modulate cellular stress and secretory pathways to restore proteostasis.

Our approach builds on the success of pharmacological chaperones, a strategy exemplified by tafamidis—a groundbreaking treatment for transthyretin amyloidosis—discovered and developed by our cofounders, Dr. Jeffery W. Kelly and Dr. Richard Labaudinière.

We also expand on the principle of correcting imbalances in protein homeostasis by using small molecules to activate the unfolded protein response (UPR). This targeted activation enhances the cell’s capacity to fold proteins, addressing underlying pathologies associated with misfolded proteins.

Pipeline

Advancing key programs targeting diseases with high unmet needs.

Careers

At Protego Bio, we value innovation, dedication, and a passion for advancing science. We are always seeking exceptional talent to join our dynamic team.

If you believe your skills and expertise align with our mission, we encourage you to submit your resume and cover letter to Careers@protegobio.com

We will keep your information on file and contact you if a suitable opportunity arises.