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

© 2023. The Author(s)..

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.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:29

Enthalten in:

Nature medicine - 29(2023), 10 vom: 28. Okt., Seite 2615-2624

Sprache:

Englisch

Beteiligte Personen:

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

Links:

Volltext

Themen:

Clinical Trial, Phase II
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 23.10.2023

Date Revised 23.11.2023

published: Print-Electronic

ClinicalTrials.gov: NCT03188666

Citation Status MEDLINE

doi:

10.1038/s41591-023-02561-8

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM362668701