BackgroundABX464 upregulates the expression of the anti-inflammatory microRNA miR-124 and is a first-in-class drug candidate as an oral treatment for moderate-to-severe Rheumatoid Arthritis (RA).ObjectivesThis phase 2a randomized, double blind, placebo controlled, parallel group 12-week study evaluated the safety and preliminary efficacy of ABX464 (50 and 100 mg q.d.), in combination with methotrexate (MTX) in 60 patients (1:1:1 ratio) with moderate-to-severe active RA who have inadequate response to MTX or/and to an anti-TNFα therapy. Patients who completed the 12-week induction phase could roll over into a 52-week open-label maintenance study to evaluate the long-term safety and efficacy of 50 mg q.d oral ABX464 in RA.MethodsThe primary end point was the safety of ABX464; efficacy endpoints included the proportion of patients achieving ACR20/50/70 responses, disease activity scores (DAS28, SDAI, CDAI), EULAR response, DAS28 low disease activity (DAS28-CRP ≤ 3.2) or remission. Blood samples from patients were used to measure the expression of miR-124 and the relative concentrations of cytokines (baseline and week 8).ResultsPatients baseline characteristics were well balanced in terms of disease severity and demographics (mean ± SD DAS28-CRP: 5.43 ± 0.78; RA duration: 6.43 ± 7.43 years). ABX464 50 mg was safe and well tolerated. Two serious adverse events (SAEs) were reported (one on placebo group and one on ABX464 100 mg). Eleven patients were withdrawn for AEs (9 patients on 100 mg, 1 on 50 mg and 1 on placebo). An increased incidence of largely mild-to-moderate gastrointestinal AEs in the 100 mg treatment group led to a higher drop-out rate of patients. The nature of these AEs was consistent with what has been observed in more than 1023 subjects who have so far been treated in other clinical trials with ABX464 across different indications. No cases of opportunistic infection, no malignancies and no death were reported.Although the sample size of this proof-of-concept study was not powered to show efficacy, multiple early efficacy endpoints showed signs of promise with the ABX464 50 mg daily dose. Compared to placebo, ABX464 50 mg showed significantly higher proportions of patients achieving ACR20 and ACR50 responses at week 12 in the per protocol population (PP). DAS28-CRP and DAS28-ESR decreased significantly (Intent-to-Treat Population, ITT) and rates of categorical DAS28-CRP response (PP) or CDAI remission (ITT) increased significantly on ABX464 at week 12 (Table 1). Compared to placebo, a significant upregulation of miR-124 expression and a decrease in IL-6 blood levels were observed for every patient dosed with ABX464.Table 1.Efficacy endpoints.Placebo50 mg100 mgPPITTPPITTPPITT(n=19)(n=20)(n=16)(n=21)(n=7)(n=19)Early discontinuations due to AE119 ACR20 n (%)4 (21%)4 (20%)9 (56%) *9 (43%)3 (43%)3 (16%) ACR50 n (%)1 (5%)1 (5%)5 (31%) *5 (24%)2 (29%)2 (11%) ACR70 n (%)1 (5%)1 (5%)4 (25%)4 (19%)1 (14%)1 (5%)DAS28-CRP-0.63-0.60-1.79 *-1.41 *-1.94 *-0,72Mean change from baselineDAS28-ESR-0.65-0.59-1.86 *-1.43 *-2.0 **-0.74Mean change from baselineLow Disease Activity2 (11%)2 (10%)4 (25%)4 (19%)3 (43%)3 (16%)(DAS28-CRP ≤ 3.2) n (%)Categorical DAS28-CRP response8 (42%)8 (40%)14 (88%) **14 (67%)6 (86%) *6 (32%)n (%)CDAI ≤ 10 n (%)2 (11%)2 (10%)5 (31%)5 (24%)3 (43%)3 (16%)CDAI Remission n (%)003 (19%) *3 (14%) *00* P < 0.05, ** P < 0.01 Chi-squared test ABX-464 versus placebo40 patients enrolled in the ongoing open-label maintenance study with ABX464 50 mg q.d.At week 52, the drop-out rate of patients was 44 % (17/39), including 7 drop-outs due to AE (18 %). Preliminary maintenance efficacy data, defined as Low Disease Activity, were obtained from 22 patients who reached 52 weeks of treatment: 44 % patients achieved LDA according to ITT.ConclusionEfficacy and safety findings of the first-in-class drug candidate ABX464 warrant further exploration at 50 mg q.d. or less as an oral treatment for RA patients.Disclosure of InterestsClaire Daien Speakers bureau: Abivax, Consultant of: Abivax, Abbvie, Amgen, BMS, Fresenius-Kabi, MSD, Novartis, Pfizer, Sandoz, Sanofi, Roche-Chugai, UCB, Grant/research support from: punctual links or research grant from Abbvie, Amgen, BMS, Fresenius-Kabi, MSD, Novartis, Pfizer, Sandoz, Sanofi, Roche-Chugai, UCB, Marek Krogulec: None declared, Paul Gineste Employee of: Abivax, Jean-Marc Steens Employee of: Abivax, Laurence Desroys Du Roure Employee of: Abivax, Sophie Biguenet Employee of: Abivax, Didier Scherrer Employee of: Abivax, Julien Santo Employee of: Abivax, Hartmut Ehrlich Employee of: Abivax, Patrick Durez: None declared