Investigational drugs inhibiting complement for the treatment of geographic atrophy

被引:4
|
作者
Desideri, Lorenzo Ferro [1 ,2 ,4 ]
Artemiev, Dmitri [1 ]
Bernardi, Enrico [1 ]
Paschon, Karin [1 ]
Zandi, Souska [1 ,2 ]
Zinkernagel, Martin [1 ,2 ]
Anguita, Rodrigo [1 ,3 ]
机构
[1] Univ Bern, Bern Univ Hosp, Dept Ophthalmol, Inselspital, Bern, Switzerland
[2] Univ Bern, Bern Univ Hosp, Bern Photog Reading Ctr, Inselspital, Bern, Switzerland
[3] Moorfields Eye Hosp NHS Fdn Trust, London, England
[4] Univ Bern, Bern Univ Hosp, Dept Ophthalmol, Inselspital, Freiburgstr 15, CH-3010 Bern, Switzerland
关键词
Geographic atrophy; GA; macular degeneration; AMD; complement cascade; pegcetacoplan; lampalizumab; avacincaptad pegol; PATHWAY; VARIANT; LECTIN; C3;
D O I
10.1080/13543784.2023.2276759
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionGeographic atrophy (GA) is a progressive form of age-related macular degeneration (AMD) that leads to severe visual impairment and central vision loss. Traditional treatment options for GA are limited, highlighting the need for new therapeutic approaches. In recent years, targeting the complement system has emerged as a promising strategy for the treatment of GA.Areas coveredThis expert opinion article reviews the investigational drugs inhibiting the complement cascade for the treatment of GA. Specifically, it focuses on the recent FDA approved pegcetacoplan, a C3 complement inhibitor, and avacincaptad pegol, a C5 complement inhibitor, highlighting their potential efficacy and safety profiles based on clinical trial data.Expert opinionFDA approval of intravitreal pegcetacoplan and avacincaptad pegol marks significant progress in the landscape of GA treatment. However, variable results from trials underscore the complex nature of GA and the importance of patient selection. Complement inhibition holds promise, but ongoing research is vital to refine treatment strategies and offer improved outcomes for GA patients.
引用
收藏
页码:1009 / 1016
页数:8
相关论文
共 50 条
  • [31] Complement Inhibition for Geographic Atrophy: A Tempting Target with Mixed Results
    Lin, Jonathan B.
    Halawa, Omar A.
    Miller, Joan W.
    Vavvas, Demetrios G.
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (13)
  • [32] Complement inhibition treatment for geographic atrophy (GA): functional and morphological efficacy and relevant biomarkers in clinical practice
    Schmidt-Erfurth, Ursula
    Riedl, Sophie
    OPHTHALMOLOGIE, 2024, 121 (06): : 476 - 481
  • [33] Ethics framework for treatment use of investigational drugs
    Jan Borysowski
    Andrzej Górski
    BMC Medical Ethics, 21
  • [34] Synthetic investigational new drugs for the treatment of tuberculosis
    Kwon, Yong-Soo
    Koh, Won-Jung
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2016, 25 (02) : 183 - 193
  • [35] Experimental and investigational drugs for the treatment of anal cancer
    Jacome, Alexandre A.
    Eng, Cathy
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2018, 27 (12) : 941 - 950
  • [36] Current and investigational drugs for the treatment of diabetic retinopathy
    Tolentino, Michael Steven
    Tolentino, Andrew John
    Tolentino, Michael John
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2016, 25 (09) : 1011 - 1022
  • [37] Investigational drugs for the treatment of kidney transplant rejection
    van Vugt, Lukas K.
    Schagen, Maaike R.
    de Weerd, Annelies
    Reinders, Marlies Ej
    de Winter, Brenda Cm
    Hesselink, Dennis A.
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2022, 31 (10) : 1087 - 1100
  • [38] Investigational drugs for treatment of juvenile idiopathic arthritis
    Mauro, Angela
    Rigante, Donato
    Cimaz, Rolando
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2017, 26 (04) : 381 - 387
  • [39] Ethics framework for treatment use of investigational drugs
    Borysowski, Jan
    Gorski, Andrzej
    BMC MEDICAL ETHICS, 2020, 21 (01)
  • [40] Investigational drugs under development for the treatment of PTSD
    Ragen, Benjamin J.
    Seidel, Jordan
    Chollak, Christine
    Pietrzak, Robert H.
    Neumeister, Alexander
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2015, 24 (05) : 659 - 672