Drug intelligence / Profile preview

Myr-T3

Development stage
Preclinical
Lead developer
Amsterdam UMC
Modality
Peptide-Drug Conjugates → Peptide Conjugates → Peptides
Administration
Subcutaneous
01

Overview

Myr-T3 is a peptide-drug conjugate consisting of Myrcludex B (bulevirtide), a synthetic peptide targeting the liver-specific bile salt transporter sodium taurocholate co-transporting polypeptide (NTCP), chemically conjugated to triiodothyronine (T3), a thyroid hormone [3181]. Developed by Amsterdam UMC and Novo Nordisk, Myr-T3 is designed for liver-specific delivery of T3 to enhance hepatic lipid metabolism and treat metabolic dysfunction-associated steatotic liver disease (MASLD) and hypercholesterolemia, while minimizing the systemic cardiovascular and skeletal toxicities typically associated with thyroid hormone administration [3181]. Preclinical studies have demonstrated that Myr-T3 preserves the biological activity of both components, showing hepatic efficacy in reducing plasma cholesterol and upregulating T3-responsive genes in the liver, though further structural optimization is required to improve its organ specificity and prevent systemic toxicity at high doses [3181].

Other names
Myr-T3 fusionMyr-T-3 fusionMyr-T 3 fusionMyrcludex B-T3 conjugateMyrcludex B-triiodothyronine conjugate
02

Targets

NTCP (Na+-taurocholate cotransporting polypeptide)

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