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Abatacept in individuals at high risk of rheumatoid arthritis (APIPPRA): a randomised, double-blind, multicentre, parallel, placebo-controlled, phase 2b clinical trial

Title: Abatacept in individuals at high risk of rheumatoid arthritis (APIPPRA): a randomised, double-blind, multicentre, parallel, placebo-controlled, phase 2b clinical trial
Authors: Cope AP; Jasenecova M; Vasconcelos JC; Filer A; Raza K; Qureshi S; D'Agostino MA; McInnes IB; Isaacs JD; Pratt AG; Fisher BA; Buckley CD; Emery P; Ho P; Buch MH; Ciurtin C; van Schaardenburg D; Huizinga T; Toes R; Georgiou E; Kelly J; Murphy C; Prevost AT; Norton S; Lempp H; Opena M; Subesinghe S; Garrood T; Menon B; Ng N; Douglas K; Koutsianas C; Cooles F; Falahee M; Echavez-Naguicnic I; Bharadwaj A; Villaruel M; Pande I; Collins D; Pegler S; Raizada S; Siebert S; Fragoulis G; Guinto J; Galloway J; Rutherford A; Barnes T; Jeffrey H; Patel Y; Batley M; O'Reilly B; Venkatachalam S; Sheeran T; Gorman C; Reynolds P; Khan A; Gullick N; Banerjee S; Mankia K; Jordan D; Rowlands J; Starmans-Kool M; Taylor J; Nandi P; Sahbudin I; Maybury M; Hider S; Barcroft A; McNally J; Kitchen J; Nisar M; Quick V
Source: The Lancet, 2024
Publisher Information: Elsevier BV
Publication Year: 2024
Collection: Newcastle University Library ePrints Service
Description: © 2024 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Background: Individuals with serum antibodies to citrullinated protein antigens (ACPA), rheumatoid factor, and symptoms, such as inflammatory joint pain, are at high risk of developing rheumatoid arthritis. In the arthritis prevention in the pre-clinical phase of rheumatoid arthritis with abatacept (APIPPRA) trial, we aimed to evaluate the feasibility, efficacy, and acceptability of treating high risk individuals with the T-cell co-stimulation modulator abatacept. Methods: The APIPPRA study was a randomised, double-blind, multicentre, parallel, placebo-controlled, phase 2b clinical trial done in 28 hospital-based early arthritis clinics in the UK and three in the Netherlands. Participants (aged ≥18 years) at risk of rheumatoid arthritis positive for ACPA and rheumatoid factor with inflammatory joint pain were recruited. Exclusion criteria included previous episodes of clinical synovitis and previous use of corticosteroids or disease-modifying antirheumatic drugs. Participants were randomly assigned (1:1) using a computer-generated permuted block randomisation (block sizes of 2 and 4) stratified by sex, smoking, and country, to 125 mg abatacept subcutaneous injections weekly or placebo for 12 months, and then followed up for 12 months. Masking was achieved by providing four kits (identical in appearance and packaging) with pre-filled syringes with coded labels of abatacept or placebo every 3 months. The primary endpoint was the time to development of clinical synovitis in three or more joints or rheumatoid arthritis according to American College of Rheumatology and European Alliance of Associations for Rheumatology 2010 criteria, whichever was met first. Synovitis was confirmed by ultrasonography. Follow-up was completed on Jan 13, 2021. All participants meeting the intention-to-treat principle were included in the analysis. This trial was registered with EudraCT (2013–003413–18). Findings: Between Dec 22, ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/296952; https://eprints.ncl.ac.uk/fulltext.aspx?url=296952/4D8D5159-788B-4D2E-AE23-66F7A88486DF.pdf&pub_id=296952
Availability: https://eprints.ncl.ac.uk/296952
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.EDA97D2E
Database: BASE