Pharmacokinetics, Pharmacodynamics (PK/PD), and Safety Profile of Ulviprubart: Results from a 48-week, Open-label, Phase 1 Study in Patients with Inclusion Body Myositis (IBM) (P3-11.012)

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Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000211798
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
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article

Pharmacokinetics, Pharmacodynamics (PK/PD), and Safety Profile of Ulviprubart: Results from a 48-week, Open-label, Phase 1 Study in Patients with Inclusion Body Myositis (IBM) (P3-11.012)

Christina Liang, Dulce Soler-Ferran, H. Jeffrey Wilkins, Robert D. Henderson et al.
5 links
Neurology
Inflammatory Myopathies and Dermatomyositis
article

Pharmacokinetics, Pharmacodynamics (PK/PD), and Safety Profile of Ulviprubart: Results from a 48-week, Open-label, Phase 1 Study in Patients with Inclusion Body Myositis (IBM) (P3-11.012)

Christina Liang, Dulce Soler-Ferran, H. Jeffrey Wilkins, Robert D. Henderson, Merrilee Needham, Steven A. Greenberg
article en

Abstract

No abstract available for this paper.
NeurologyVol. 104(7_Supplement_1)
University of Notre Dame (US), Brigham and Women's Hospital (US), The University of Queensland (AU), Murdoch University (AU), Royal Brisbane and Women's Hospital (AU), Royal North Shore Hospital (AU), Fiona Stanley Hospital (AU)
Openalex Percentile: Top 90%
Inflammatory Myopathies and Dermatomyositis
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Pharmacokinetics, Pharmacodynamics (PK/PD), and Safety Profile of Ulviprubart: Results from a 48-week, Open-label, Phase 1 Study in Patients with Inclusion Body Myositis (IBM) (P3-11.012) — Christina Liang, Dulce Soler-Ferran, et al. · Neurology (2025) | TGRS Research Map | TGRS