Results from a first-in-human study of dersimelagon, an investigational oral selective MC1R agonist

• Published in: European journal of clinical pharmacology Vol. 79; no. 6; pp. 801 - 813
• Main Authors: Ogasawara, Akihito, Ogawa, Kei, Ide, Ryosuke, Ikenaga, Yuka, Fukunaga, Chie, Nakayama, Satoshi, Tsuda, Minoru
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.06.2023; Springer Nature B.V
• Subjects: Administration, Oral; Agonists; Area Under Curve; Biomedical and Life Sciences; Biomedicine; Dosage; Dose-Response Relationship, Drug; Double-Blind Method; Erythropoietic protoporphyria; Healthy Volunteers; Humans; Hyperpigmentation; Melanin; Pharmacodynamics; Pharmacokinetics; Pharmacology/Toxicology; Population studies; X-linked protoporphyria; First-in human; Dersimelagon; Melanin density; Erythropoietic protoporphyria
• ISSN: 0031-6970; 1432-1041
• DOI: 10.1007/s00228-023-03476-6

Purpose To describe outcomes from the first-in-human study of dersimelagon, an investigational oral selective MC1R agonist, under development for the treatment of erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP). Methods In this double-blind, placebo-controlled phase 1 study, the safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple ascending oral doses of dersimelagon in healthy participants were evaluated. Results Dersimelagon was generally well tolerated in healthy participants, with the most common TEAEs being lentigo (52.8%) and skin hyperpigmentation (50.0%) after multiple doses. Systemic exposure to dersimelagon in plasma (based on AUC 0-∞ and C max ) increased in a slightly more than dose-proportional manner over the 1- to 600-mg single-dose range. Following multiple doses, dersimelagon was rapidly absorbed (median T max ranging from 4 to 5 h postdose on days 1 and 14). Mean t 1/2 ranged from 10.56 to 18.97 h on day 14, and the steady state of plasma concentration was generally reached by 5 days of multiple dosing. There were no observable effects of age or race on the PK profile of dersimelagon or its metabolite dersimelagon glucuronide. No treatment-related effects on melanin density (MD) were observed following single doses of dersimelagon; however, after multiple doses, increases in MD were observed in participants receiving 150 and 300 mg dersimelagon. Conclusion Our study results indicate that dersimelagon is generally well tolerated and demonstrates a generally consistent PK profile across diverse subgroups. Treatment-related increases in MD warrant further investigation in a larger study population and in patients with EPP and XLP. Trial registration A Study to Investigate the Safety, Tolerability and Pharmacokinetics of MT-7117 in Healthy Subjects, NCT02834442, https://clinicaltrials.gov/ct2/show/NCT02834442 , registration began July 2016.