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)
Authors
Christina Liang (ORCID: https://orcid.org/0000-0002-2503-1917)
Dulce Soler-Ferran
H. Jeffrey Wilkins
Robert D. Henderson (ORCID: https://orcid.org/0000-0002-2820-8183)
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.
Local Database Links
5 links
Journal
Neurology
Topics
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.
Publication Tag
NeurologyVol. 104(7_Supplement_1)
Institutions
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)
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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