Discovery of Zilucoplan: A Complement C5 Inhibitor for Treatment of Anti-Acetylcholine Receptor (AChR) Antibody-Positive Generalized Myasthenia Gravis (gMG)

Complement component 5 (C5) is a protein in the complement cascade and a part of the innate immune system that has been clinically validated as a therapeutic target for several immune-mediated diseases including generalized myasthenia gravis (gMG). In this paper, we discuss the early discovery of zilucoplan, a macrocyclic peptide drug, which was identified via innovative extreme diversity mRNA display (Ma, Z.; Hartman, M. C. T. In Vitro Selection of Unnatural Cyclic Peptide Libraries via mRNA Display. In <i>Ribosome Display and Related Technologies: Methods and Protocols</i>; Douthwaite, J. A., Jackson, R. H., Eds.; Springer: New York, 2012; pp 367-390.) against C5 and approved for the treatment of gMG. We highlight the key steps and rationale behind the peptide medicinal chemistry optimization of the initial screening hits, that led to improved potency, stability, and pharmacokinetic properties.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-12-11
DOI
https://doi.org/10.1021/acs.jmedchem.5c02537
Citations
1
Primary Topic
Myasthenia Gravis and Thymoma
Type
article
Field-Weighted Citation Impact
1.39
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article

Discovery of Zilucoplan: A Complement C5 Inhibitor for Treatment of Anti-Acetylcholine Receptor (AChR) Antibody-Positive Generalized Myasthenia Gravis (gMG)

Ketki Dhamnaskar, Michelle D. Hoarty, Ping Ye, Steven J. DeMarco et al.
1 citations
Journal of Medicinal Chemistry
Myasthenia Gravis and Thymoma
1.39
article

Discovery of Zilucoplan: A Complement C5 Inhibitor for Treatment of Anti-Acetylcholine Receptor (AChR) Antibody-Positive Generalized Myasthenia Gravis (gMG)

Ketki Dhamnaskar, Michelle D. Hoarty, Ping Ye, Steven J. DeMarco, Guoqing Tang, Zhaolin Wang, Robert P. Hammer, Alonso Ricardo, Zhong Ma
article en
1 citations

Abstract

Complement component 5 (C5) is a protein in the complement cascade and a part of the innate immune system that has been clinically validated as a therapeutic target for several immune-mediated diseases including generalized myasthenia gravis (gMG). In this paper, we discuss the early discovery of zilucoplan, a macrocyclic peptide drug, which was identified via innovative extreme diversity mRNA display (Ma, Z.; Hartman, M. C. T. In Vitro Selection of Unnatural Cyclic Peptide Libraries via mRNA Display. In <i>Ribosome Display and Related Technologies: Methods and Protocols</i>; Douthwaite, J. A., Jackson, R. H., Eds.; Springer: New York, 2012; pp 367-390.) against C5 and approved for the treatment of gMG. We highlight the key steps and rationale behind the peptide medicinal chemistry optimization of the initial screening hits, that led to improved potency, stability, and pharmacokinetic properties.

Journal of Medicinal ChemistryVol. 68(24)
AVEO Oncology (United States) (US), Bioscience Research (US), Factor Bioscience (United States) (US)
Openalex Percentile: Top 13%
Myasthenia Gravis and Thymoma
1.39
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