Open-label study characterizes pharmacokinetics, efficacy, and safety of tanruprubart in participants with GBS, suggesting potential treatment benefits.
Characterize the pharmacokinetics, pharmacodynamics, efficacy, and safety of tanruprubart 30 mg/kg in participants with Guillain-Barré syndrome (GBS) from North America and Europe.
No takes yet. Share an insight, caveat, or question.
Ladha et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: