Development and validation of a novel analytical method for related substances of resmetirom and identification of new degradation products

Background Resmetirom (MGL-3196), a highly selective thyroid hormone receptor β agonist, is indicated for treating adults with noncirrhotic nonalcoholic steatohepatitis (NASH) exhibiting moderate to advanced liver fibrosis. Related substances are critical factors that directly impact the safety and efficacy of the active pharmaceutical ingredient (API). Therefore, the quantitative detection of related substances in resmetirom is of particular importance. Methods This study established a reverse-phase high-performance liquid chromatography (RP-HPLC) for the separation of resmetirom and its related substances. The analysis was performed using an Agilent 5 HC C 18 (2) column (250 mm × 4.6 mm, 5 µm) at 35 °C, with detection at 220 nm. A gradient elution method was employed, achieving effective separation of all impurities within a 45-min runtime. The final HPLC method utilized with a mixture of H 2 O/ACN (90/10, v/v) containing 0.045% TFA as mobile phase A, and ACN as mobile phase B. The gradient elution proceeded as follows: 0–2 min, 10% B→ 10% B; 2–20 min, 10% B→ 50% B; 20–30 min, 50% B→ 54% B; 30–35 min, 54% B→ 54% B; 35–36 min, 54% B→ 10% B; and 36–45 min, 10% B→ 10% B. The rate of flow was 1.0 mL/min. A 10 µL volume was used for the sample injection. Results The method was validated according to International Conference on Harmonization (ICH) guidelines, and the results demonstrated that it possesses good specificity, stability, linearity, precision, repeatability, and robustness. Furthermore, a new degradation product, designated as imp-A, was generated under alkaline degradation conditions in this study. Its chemical structure was elucidated using nuclear magnetic resonance (NMR) and high-resolution mass spectrometry (HRMS), and this compound has been reported for the first time. Conclusion The RP-HPLC method established in this study is capable of accurately and reliably separating and detecting resmetirom and its related substances. The method is simple to operate and yields dependable results, providing a practical and efficient analytical tool for the quality control of resmetirom and its formulations. This contributes to ensuring the safety and efficacy of the drug product.

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Publication Details

Journal
Frontiers in Chemistry
Published
2026-03-24
DOI
https://doi.org/10.3389/fchem.2026.1795082
Primary Topic
Pharmacological Effects and Assays
Type
article
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article

Development and validation of a novel analytical method for related substances of resmetirom and identification of new degradation products

Frontiers in Chemistry
Pharmacological Effects and Assays
article

Development and validation of a novel analytical method for related substances of resmetirom and identification of new degradation products

article en

Abstract

Background Resmetirom (MGL-3196), a highly selective thyroid hormone receptor β agonist, is indicated for treating adults with noncirrhotic nonalcoholic steatohepatitis (NASH) exhibiting moderate to advanced liver fibrosis. Related substances are critical factors that directly impact the safety and efficacy of the active pharmaceutical ingredient (API). Therefore, the quantitative detection of related substances in resmetirom is of particular importance. Methods This study established a reverse-phase high-performance liquid chromatography (RP-HPLC) for the separation of resmetirom and its related substances. The analysis was performed using an Agilent 5 HC C 18 (2) column (250 mm × 4.6 mm, 5 µm) at 35 °C, with detection at 220 nm. A gradient elution method was employed, achieving effective separation of all impurities within a 45-min runtime. The final HPLC method utilized with a mixture of H 2 O/ACN (90/10, v/v) containing 0.045% TFA as mobile phase A, and ACN as mobile phase B. The gradient elution proceeded as follows: 0–2 min, 10% B→ 10% B; 2–20 min, 10% B→ 50% B; 20–30 min, 50% B→ 54% B; 30–35 min, 54% B→ 54% B; 35–36 min, 54% B→ 10% B; and 36–45 min, 10% B→ 10% B. The rate of flow was 1.0 mL/min. A 10 µL volume was used for the sample injection. Results The method was validated according to International Conference on Harmonization (ICH) guidelines, and the results demonstrated that it possesses good specificity, stability, linearity, precision, repeatability, and robustness. Furthermore, a new degradation product, designated as imp-A, was generated under alkaline degradation conditions in this study. Its chemical structure was elucidated using nuclear magnetic resonance (NMR) and high-resolution mass spectrometry (HRMS), and this compound has been reported for the first time. Conclusion The RP-HPLC method established in this study is capable of accurately and reliably separating and detecting resmetirom and its related substances. The method is simple to operate and yields dependable results, providing a practical and efficient analytical tool for the quality control of resmetirom and its formulations. This contributes to ensuring the safety and efficacy of the drug product.

Frontiers in ChemistryVol. 14
Nanchang University (CN), Nantong University (CN), Affiliated Hospital of Nantong University (CN), China National Pharmaceutical Group Corporation (China) (CN), First Affiliated Hospital of Jiangxi Medical College (CN)
Openalex Percentile: Top 8%
Pharmacological Effects and Assays
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