Successful treatment with avacopan (CCX168) in a pediatric patient with C3 glomerulonephritis.

Author: CappoliAndrea, Diomedi-CamasseiFrancesca, EmmaFrancesco, GargiuloAntonio, VivarelliMarina, ZottaFederica

Paper Details 
Original Abstract of the Article :
C3 glomerulonephritis (C3GN) is a subtype of C3 glomerulopathy (C3G), characterized by dysregulation of the alternative pathway of complement and by dominant C3 by immunofluorescence on the kidney biopsy. There is no approved treatment for patients with C3G. Immunosuppressive drugs as well as biolog...See full text at original site
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引用元:
https://doi.org/10.1007/s00467-023-06035-4

データ提供:米国国立医学図書館(NLM)

Avacopan: A New Oasis in the Desert of C3 Glomerulonephritis

C3 glomerulonephritis (C3GN), a rare and potentially serious kidney disease, can feel like a daunting desert, with limited treatment options. This study explores the use of avacopan (CCX168), a C5aR antagonist, in a pediatric patient with C3GN, offering a glimmer of hope for a new treatment approach.

Avacopan: A Promising New Frontier

The study highlights the potential of avacopan as a treatment for C3GN, demonstrating its effectiveness in a pediatric patient. The study's findings suggest that avacopan, like a spring of water in a barren desert, could offer a vital source of relief for individuals with this challenging condition.

A New Path for Treatment: Targeting the Complement System

This research offers hope for a new approach to treating C3GN, focusing on the complement system. The study's findings suggest that avacopan could potentially play a role in managing this complex and often debilitating disease.

Dr.Camel's Conclusion

This case study offers a promising glimpse into the potential of avacopan as a treatment for C3 glomerulonephritis, offering a new path to hope for individuals facing this challenging condition. Just as a camel navigates a desert seeking a source of water, so too do researchers explore new avenues for treating diseases, seeking solutions to improve patient outcomes.

Date :
  1. Date Completed 2023-11-07
  2. Date Revised 2023-11-07
Further Info :

Pubmed ID

37306717

DOI: Digital Object Identifier

10.1007/s00467-023-06035-4

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Languages

English

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