Background Geographic atrophy is an advanced form of dry age-related macular degeneration that can lead to irreversible vision loss and high burden of disease. We aimed to assess efficacy and safety of avacincaptad pegol 2 mg in reducing geographic atrophy lesion growth.Methods GATHER2 is a randomised, double-masked, sham-controlled, 24-month, phase 3 trial across 205 retina clinics, research hospitals, and academic institutions globally. To be eligible, patients had to be aged 50 years or older with non-centrepoint-involving geographic atrophy and best corrected visual acuity between 20/25 and 20/320 in the study eye. Eligible patients were randomly assigned (1:1) to monthly avacincaptad pegol 2 mg administered as a 100 mu L intravitreal injection or sham for the first 12 months. Randomisation was performed using an interactive response technology system with stratification by factors known to be of prognostic importance in age-related macular degeneration. Patients, investigators, study centre staff, sponsor personnel, and data analysts were masked to treatment allocation. The primary endpoint was geographic atrophy lesion size measured by fundus autofluorescence at baseline, month 6, and month 12. Efficacy and safety analyses were done in the modified intention-to-treat and safety populations, respectively. This trial is registered with ClinicalTrials.gov, NCT04435366.Findings Between June 22, 2020, and July 23, 2021, 1422 patients were screened for eligibility, of whom 448 were enrolled and randomly assigned to avacincaptad pegol 2 mg (n=225) or sham (n=223). One patient in the sham group did not receive study treatment and was excluded from analyses. There were 154 (68%) female patients and 71 (32%) male patients in the avacincaptad pegol 2 mg group, and 156 (70%) female patients and 66 (30%) male patients in the sham group. From baseline to month 12, the mean rate of square-root-transformed geographic atrophy area growth was 0 center dot 336 mm/year (SE 0 center dot 032) with avacincaptad pegol 2 mg and 0 center dot 392 mm/year (0 center dot 033) with sham, a difference in growth of 0 center dot 056 mm/year (95% CI 0 center dot 016-0 center dot 096; p=0 center dot 0064), representing a 14% difference between the avacincaptad pegol 2 mg group and the sham group. Ocular treatment-emergent adverse events in the study eye occurred in 110 (49%) patients in the avacincaptad pegol 2 mg group and 83 (37%) in the sham group. There were no endophthalmitis, intraocular inflammation, or ischaemic optic neuropathy events over 12 months. To month 12, macular neovascularisation in the study eye occurred in 15 (7%) patients in the avacincaptad pegol 2 mg group and nine (4%) in the sham group, with exudative macular neovascularisation occurring in 11 (5%) in the avacincaptad pegol 2 mg group and seven (3%) in the sham group.Interpretation Monthly avacincaptad pegol 2 mg was well tolerated and showed significantly slower geographic atrophy growth over 12 months than sham treatment, suggesting that avacincaptad pegol might slow disease progression and potentially change the trajectory of disease for patients with geographic atrophy.Funding Iveric Bio, An Astellas Company.Copyright (c) 2023 Elsevier Ltd. All rights reserved.

Efficacy and safety of avacincaptad pegol in patients with geographic atrophy (GATHER2): 12-month results from a randomised, double-masked, phase 3 trial / Khanani, Arshad M; Patel, Sunil S; Staurenghi, Giovanni; Tadayoni, Ramin; Danzig, Carl J; Eichenbaum, David A; Hsu, Jason; Wykoff, Charles C; Heier, Jeffrey S; Lally, David R; Monés, Jordi; Nielsen, Jared S; Sheth, Veeral S; Kaiser, Peter K; Clark, Julie; Zhu, Liansheng; Patel, Hersh; Tang, Justin; Desai, Dhaval; Jaffe, Glenn J; Alezzandrini, Arturo; Francone, Anibal Andres; Bafalluy, Joaquín; Bainttein, Silvina; Luna Pinto, Jose; Saravia, Mario; Vidosevich, Matko; Zeolite, Carlos; Furno Sola, Federico; Chang, Andrew; Cornish, Elisa Eleanor Guida; Nguyen, Thanh; Findl, Oliver; Haas, Anton; Kralinger, Martina; Sacu, Stefan; Postelmans, Laurence Dominique; Farah, Michel; Maia, Mauricio; Nehemy, Marcio; Ali, Fareed; Brent, Michael; Dollin, Michael; Gonder, John; Kherani, Amin; Merkur, Andrew; Tuli, Raman; Lopera, Monica Marie; Rodriguez, Francisco; Bradvica, Mario; Ernest, Jan; Kalijurand, Kuldar; Noor, Kai; Cohen, Yves; Creuzot-Garcher, Catherine; De Bats, Flore; Devin, François; Français-Maury, Catherine; Kodjikian, Laurent; Korobelnik, Jean François; Le Mer, Yannick; Quaranta El Maftouhi, Maddalena; Razavi, Sam; Souied, Eric; Tadayoni, Ramin; Weber, Michel; Eter, Nicole; Feltgen, Nicolas; Grisanti, Salvatore; Walter, Peter; Liegl, Raffael; Lorenz, Katrin; Spital, Georg; Priglinger, Siegfried; Spitzer, Martin; Volker, Michael; Krohne, Tim; Jochmann, Claudia; Lohmann, Chris Patrick; Framme, Carsten; Kerenyi, Agnes; Papp, Andras; Seres, Andras; Toth-Molnar, Edit; Tsorbatzoglou, Alexis; Vajas, Atilla; Varsanyi, Balázs; Vogt, Gabor; Bar, Asaf; Eting, Eva; Hauser, David; Levy, Jamie; Mathalone, Nurit; Morori-Katz, Haia; Rosenblatt, Irit; Soudry-Zayit, Shiri; Trivizky, Omert; Bandello, Francesco; Ciardella, Antonio Pasquale; Figus, Michele; Giansanti, Fabrizio; Lanzetta, Paolo; Mariotti, Cesare; Mastropasqua, Leonardo; Midena, Edoardo; Parmeggiani, Francesco; Ricci, Federico; Simonelli, Francesca; Staurenghi, Giovanni; Viola, Francesco; Varano, Monica; Laganovska, Guna; Cisiecki, Sławomir; Jedrzejewski, Wojciech; Kaluzny, Jakub; Misiuk-Hojło, Marta; Abengoechea, Santiago; Iribarren, Javier Araiz; Ascaso, Franciso Javier; Cubero, Juan Manuel; Gallego-Pinazo, Roberto; Gomez-Ulla De Irazazabal, Francisco; Mestre, Ignasi Jürgens; Mones I Carilla, Jordi Manel; Montero Moreno, Javier; María Ruiz Moreno, José; Sararols Ramsay, Laura; Garcia Layana, Alfredo; Downey, Louise; Abraham, Prema; Alfaro, Daniel Virgil; Bagheri, Nika; Barbazetto, Irene; Benevento, Joseph; Bernstein, Paul; Bertolucci, George; Bhavsar, Abdhish; Bridges, William; Brooks, Jr, Harold Logan; Brown, Jamin; Brucker, Alexander; Calvo, Charles M.; Capone, Antonio; Carlson, John; Chan, Clement; Chang, Emmanuel; Chan-Kai, Brian; Chaudhry, Nauman; Chen, Sanford; Csaky, Karl; Cummings, Howard; Danzig, Carl; Dessouki, Amr; Dyer, David; Eaton, Alexander; Eichenbaum, David; Faber, David; Feldman, Robert; Finnen, Neil; Freeman, William; Frenkel, Ronald; Gonzales, Christine; Gonzalez, Victor; Gross, John; Gupta, Sunil; Hall, Edward; Han, Min-Kyu; Heier, Jeffrey; Hershberger, Vrinda; Higgins, Patrick; Hsu, Jason; Ip, Michael; Jablon, Eric; Jewart, Brian; John, Vishak; Jonisch, Jonathan; Joondeph, Brian; Kay, Christine; Khanani, Arshad; Kokame, Gregg T.; Kwun, Robert; Lai, Michael; Lally, David; Laud, Ketan; Lavina, Adrian; Lee, Michael; Lin, Phoebe; Lin, Haijiang; Manoharan, Niranjan; Marcus, Dennis; Martidis, Adam; McCabe, Frank; Nielsen, Jared; Osher, James; Palmer, James; Patel, Sunil; Pearlman, Joel; Perkins, Stephen; Pirouz, Ashkan; Qureshi, Jawad; Randolph, John; Piri, Niloofar; Rosenfeld, Phillip; Saperstein, David; Scartozzi, Richard; Schwartz, Steven; Sharma, Ashish; Sharma, Atul; Sheth, Veeral; Singer, Michael; Spinak, David; Suan, Eric; Tabandeh, Homayoun; Tabassian, Ali; Uchiyama, Eduardo; Varenhorst, Michael; Wagner, Alan; Warrow, David; Wells, III, John; Wong, Robert; Wong, Keye; Wykoff, Charles; Xavier, Samantha; Ysasaga, Edward. - In: THE LANCET. - ISSN 0140-6736. - ELETTRONICO. - 402:(2023), pp. 1449-1458. [10.1016/s0140-6736(23)01583-0]

Efficacy and safety of avacincaptad pegol in patients with geographic atrophy (GATHER2): 12-month results from a randomised, double-masked, phase 3 trial

Rodriguez, Francisco;Giansanti, Fabrizio;Parmeggiani, Francesco;Viola, Francesco;
2023

Abstract

Background Geographic atrophy is an advanced form of dry age-related macular degeneration that can lead to irreversible vision loss and high burden of disease. We aimed to assess efficacy and safety of avacincaptad pegol 2 mg in reducing geographic atrophy lesion growth.Methods GATHER2 is a randomised, double-masked, sham-controlled, 24-month, phase 3 trial across 205 retina clinics, research hospitals, and academic institutions globally. To be eligible, patients had to be aged 50 years or older with non-centrepoint-involving geographic atrophy and best corrected visual acuity between 20/25 and 20/320 in the study eye. Eligible patients were randomly assigned (1:1) to monthly avacincaptad pegol 2 mg administered as a 100 mu L intravitreal injection or sham for the first 12 months. Randomisation was performed using an interactive response technology system with stratification by factors known to be of prognostic importance in age-related macular degeneration. Patients, investigators, study centre staff, sponsor personnel, and data analysts were masked to treatment allocation. The primary endpoint was geographic atrophy lesion size measured by fundus autofluorescence at baseline, month 6, and month 12. Efficacy and safety analyses were done in the modified intention-to-treat and safety populations, respectively. This trial is registered with ClinicalTrials.gov, NCT04435366.Findings Between June 22, 2020, and July 23, 2021, 1422 patients were screened for eligibility, of whom 448 were enrolled and randomly assigned to avacincaptad pegol 2 mg (n=225) or sham (n=223). One patient in the sham group did not receive study treatment and was excluded from analyses. There were 154 (68%) female patients and 71 (32%) male patients in the avacincaptad pegol 2 mg group, and 156 (70%) female patients and 66 (30%) male patients in the sham group. From baseline to month 12, the mean rate of square-root-transformed geographic atrophy area growth was 0 center dot 336 mm/year (SE 0 center dot 032) with avacincaptad pegol 2 mg and 0 center dot 392 mm/year (0 center dot 033) with sham, a difference in growth of 0 center dot 056 mm/year (95% CI 0 center dot 016-0 center dot 096; p=0 center dot 0064), representing a 14% difference between the avacincaptad pegol 2 mg group and the sham group. Ocular treatment-emergent adverse events in the study eye occurred in 110 (49%) patients in the avacincaptad pegol 2 mg group and 83 (37%) in the sham group. There were no endophthalmitis, intraocular inflammation, or ischaemic optic neuropathy events over 12 months. To month 12, macular neovascularisation in the study eye occurred in 15 (7%) patients in the avacincaptad pegol 2 mg group and nine (4%) in the sham group, with exudative macular neovascularisation occurring in 11 (5%) in the avacincaptad pegol 2 mg group and seven (3%) in the sham group.Interpretation Monthly avacincaptad pegol 2 mg was well tolerated and showed significantly slower geographic atrophy growth over 12 months than sham treatment, suggesting that avacincaptad pegol might slow disease progression and potentially change the trajectory of disease for patients with geographic atrophy.Funding Iveric Bio, An Astellas Company.Copyright (c) 2023 Elsevier Ltd. All rights reserved.
2023
402
1449
1458
Goal 3: Good health and well-being
Khanani, Arshad M; Patel, Sunil S; Staurenghi, Giovanni; Tadayoni, Ramin; Danzig, Carl J; Eichenbaum, David A; Hsu, Jason; Wykoff, Charles C; Heier, J...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1356191
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