Results 61 to 70 of about 2,004 (157)

Safety profile of complement C5 inhibitors and FcRn inhibitors in the treatment of myasthenia gravis: analysis of the FAERS database and disease-gene interaction network

open access: yesFrontiers in Immunology
ObjectiveTo integrate pharmacovigilance and network pharmacology methods for a comprehensive analysis of the potential adverse reactions of complement C5 inhibitors (eculizumab, ravulizumab, zilucoplan) and neonatal Fc receptor (FcRn) inhibitors ...
Luqiong Wang   +5 more
doaj   +1 more source

Disease Activity After Switching From Eculizumab to Ravulizumab in Patients With Paroxysmal Nocturnal Haemoglobinuria: Real World Data From Denmark and Finland

open access: yeseJHaem
Introduction Ravulizumab replaced eculizumab as the preferred complement inhibitor for Paroxysmal Nocturnal Haemoglobinuria (PNH) in Denmark and Finland after 2020. Data on real‐world disease activity after switching are limited.
Anders Rønneholt‐Frederiksen   +8 more
doaj   +1 more source

Ravulizumab as an alternative for gemcitabine related trombotic microangiopathy: A case report

open access: yesNefrología (English Edition)
Thrombotic microangiopathy (TMA) is characterized by endotelial damage, microangiopathic hemolytic anemia, thrombocytopenia and organ damage, particularly renal. In Oncology, TMA can be secondary to the cancer itself or related to oncological treatments.
Cristina Riaza Ortiz   +5 more
doaj   +1 more source

Ravulizumab for adults with generalized myasthenia gravis: a plain language summary of three studies

open access: yesJournal of Comparative Effectiveness Research
What is this summary about? Generalized myasthenia gravis (often shortened to gMG) is a rare health condition that causes muscular weakness. This summary gives an overview of three published articles that report the results of research studies of a ...
Florencia Aguirre, Renata Andrade
doaj   +1 more source

Ravulizumab for relapse prevention in AQP4-IgG–positive neuromyelitis optica spectrum disorder: a 2-year follow-up case report

open access: yesFrontiers in Medicine
BackgroundNeuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease of the central nervous system, distinct from multiple sclerosis, characterized by severe inflammatory attacks targeting the optic nerves, spinal cord, and brainstem ...
Nabil Akkawi   +2 more
doaj   +1 more source

Correlation between a 2-week change in platelet count and clinical outcomes after the initiation of ravulizumab treatment in adult patients with atypical hemolytic uremic syndrome: post-hoc analysis of the phase III trial

open access: yesThrombosis Journal
Background Atypical hemolytic uremic syndrome (aHUS) is a rare disease with poor outcomes when untreated, in which ravulizumab or eculizumab are the standard of care where available.
Masanori Matsumoto   +5 more
doaj   +1 more source

Real-World Case Series of Ravulizumab Use in Patients with Myasthenia Gravis in Romania

open access: yesBrain Sciences
Background and Objectives: Ravulizumab, a long-acting C5 complement inhibitor, was approved in the US and Europe in 2022 as an add-on therapy for the standard treatment of AChR-positive generalized MG (gMG).
Crisanda Vîlciu   +7 more
doaj   +1 more source

Assessing Preferences for Rare Disease Treatment: Qualitative Development of the Paroxysmal Nocturnal Hemoglobinuria Patient Preference Questionnaire (PNH-PPQ©)

open access: yesPatient Preference and Adherence, 2020
Karen Kaiser,1 Susan E Yount,1 Christa E Martens,1 Kimberly A Webster,1 Sara Shaunfield,1 Amy Sparling,1 John Devin Peipert,1 David Cella,1 Scott T Rottinghaus,2 Bonnie MK Donato,2 Richard Wells,3 Ioannis Tomazos2 1Department of Medical Social Sciences ...
Kaiser K   +11 more
doaj  

mRNA-1273/ravulizumab [PDF]

open access: yesReactions Weekly, 2021
openaire   +1 more source

Translating biomarker insights into practice: a path forward in TA-TMA management

open access: yesFrontiers in Medicine
Recent advances in the management of transplant-associated thrombotic microangiopathy (TA-TMA) include the harmonization of diagnostic criteria and the identification of high-risk disease features.
Sonata Jodele, Eleni Gavriilaki
doaj   +1 more source

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