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DOI 10.1038/s41591-023-02561-8

Медицинская библиотека · Nature medicine · 2023

Garetosmab in fibrodysplasia ossificans progressiva: a randomized, double-blind, placebo-controlled phase 2 trial.

Di Rocco Maja, Forleo-Neto Eduardo, Pignolo Robert J, Keen Richard, Orcel Philippe, Funck-Brentano Thomas, Roux Christian, Kolta Sami, Madeo Annalisa, Bubbear Judith S, Tabarkiewicz Jacek, Szczepanek Małgorzata, Bachiller-Corral Javier, Cheung Angela M, Dahir Kathryn M, Botman Esmée, Raijmakers Pieter G, Al Mukaddam Mona, Tile Lianne, Portal-Celhay Cynthia, Sarkar Neena, Hou Peijie, Musser Bret J, Boyapati Anita, Mohammadi Kusha, Mellis Scott J, Rankin Andrew J, Economides Aris N, Trotter Dinko Gonzalez, Herman Gary A, O'Meara Sarah J, DelGizzi Richard, Weinreich David M, Yancopoulos George D, Eekhoff E Marelise W, Kaplan Frederick S

Рандомизированное исследованиеКлиническое исследование II фазыСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Fibrodysplasia ossificans progressiva (FOP) is a rare disease characterized by heterotopic ossification (HO) in connective tissues and painful flare-ups. In the phase 2 LUMINA-1 trial, adult patients with FOP were randomized to garetosmab, an activin A-blocking antibody (n = 20) or placebo (n = 24) in period 1 (28 weeks), followed by an open-label period 2 (28 weeks; n = 43). The primary end points were safety and for period 1, the activity and size of HO lesions. All patients experienced at least one treatment-emergent adverse event during period 1, notably epistaxis, madarosis and skin abscesses. Five deaths (5 of 44; 11.4%) occurred in the open-label period and, while considered unlikely to be related, causality cannot be ruled out. The primary efficacy end point in period 1 (total lesion activity by PET-CT) was not met (P = 0.0741). As the development of new HO lesions was suppressed in period 1, the primary efficacy end point in period 2 was prospectively changed to the number of new HO lesions versus period 1. No placebo patients crossing over to garetosmab developed new HO lesions (0% in period 2 versus 40.9% in period 1; P = 0.0027). Further investigation of garetosmab in FOP is ongoing. ClinicalTrials.gov identifier NCT03188666 .

Для цитирования: Di Rocco Maja, Forleo-Neto Eduardo, Pignolo Robert J, Keen Richard, Orcel Philippe, Funck-Brentano Thomas, Roux Christian, Kolta Sami, Madeo Annalisa, Bubbear Judith S, Tabarkiewicz Jacek, Szczepanek Małgorzata, Bachiller-Corral Javier, Cheung Angela M, Dahir Kathryn M, Botman Esmée, Raijmakers Pieter G, Al Mukaddam Mona, Tile Lianne, Portal-Celhay Cynthia, Sarkar Neena, Hou Peijie, Musser Bret J, Boyapati Anita, Mohammadi Kusha, Mellis Scott J, Rankin Andrew J, Economides Aris N, Trotter Dinko Gonzalez, Herman Gary A, O'Meara Sarah J, DelGizzi Richard, Weinreich David M, Yancopoulos George D, Eekhoff E Marelise W, Kaplan Frederick S. Garetosmab in fibrodysplasia ossificans progressiva: a randomized, double-blind, placebo-controlled phase 2 trial.. Nature medicine. 2023. DOI: 10.1038/s41591-023-02561-8.

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