Safety of adalimumab biosimilar MSB11022 (acetate-buffered formulation) in patients with moderately-to-severely active rheumatoid arthritis

The AURIEL-RA study (NCT03052322; EudraCT 2016-002852-26) was a phase 3 multicenter, randomized, double-blind parallel group trial conducted from 31 January 2017 to 7 August 2018. The study was conducted in 47 centers across 6 European countries. The trial consisted of 3 periods: a 4-week screening period, a 52-week double-blind treatment period, and a 4-month safety follow-up period. Following the screening period, patients were randomized 1:1 in permuted blocks by a central interactive web response system to receive MSB11022 (acetate formulation) or reference adalimumab (Humira® citrate formulation; AbbVie Inc., North Chicago, IL, USA; European Union authorized). Patients were stratified by previous systemic therapy use: non-biologic versus biologic. Patients who previously received both biologic and non-biologic systemic therapies were assigned to the “biologic” group. The participation of patients in the previous biologic systemic therapy stratum was capped at 20% of the total number of patients randomized. The trial was double-blinded and blinding was maintained throughout the trial. Emergency unblinding did not occur. MSB11022 or reference adalimumab was administered at a dose of 40 mg subcutaneously every other week starting at baseline, up to, and including week 48.

Patients who achieved less than 20% improvement in both swollen and tender joint counts at week 24 or at any scheduled visit from week 24 up to week 52 discontinued study treatment (but participated in the safety and immunogenicity assessments).

Patients aged ≥ 18 years with a clinical diagnosis of moderately-to-severely active RA with disease duration ≥ 6 months from confirmed diagnosis were eligible for inclusion (defined by the 2010 revised American College of Rheumatology (ACR)/EULAR criteria or the 1987 Criteria of the American Rheumatology Association) [13, 14]. Patients were required to have ≥ 6 swollen joints and ≥ 6 tender joints (from the 66/68 joint count system) at screening and randomization, and either erythrocyte sedimentation rate (ESR) ≥ 28 mm/h or serum C-reactive protein (CRP) ≥ 1.0 mg/dl at screening. Patients were treated with methotrexate for ≥ 12 weeks prior to baseline with both a stable route of administration (oral or parenteral) and stable dose (10–25 mg/week) for ≥ 4 weeks prior to screening. Patients were required to be adalimumab-naïve and to have discontinued infliximab, certolizumab pegol, or golimumab at least 8 weeks prior to screening. Etanercept had to be discontinued 4 weeks prior to screening. Exposure to previous biologics was limited to one TNFα inhibitor other than adalimumab. Patients had to have no history of tuberculosis, no active tuberculosis, and no history or evidence of latent tuberculosis. Detailed exclusion criteria and prohibited medications are listed in Online Resource 2.

All subjects provided written informed consent. The study was conducted in accordance with the current International Council for Harmonisation Good Clinical Practice and the Declaration of Helsinki as well as with applicable local regulations.

The primary endpoint was the incidence of treatment-emergent adverse events of special interest (AESIs) (predefined as hypersensitivity according to Standardized MedDRA Queries [narrow] as per the latest MedDRA version) up to and including week 52. The key secondary endpoint was ACR20 at week 12 (defined as improvement of ≥ 20% from baseline in the ACR core set of measurements) [15]. Other secondary efficacy endpoints included ACR20 at weeks 2, 4, 8, and 52, and assessments of ACR50, ACR70, Disease Activity Score 28-joint count-ESR (DAS28-ESR), Clinical Disease Activity Index (CDAI), Simplified Disease Activity Index (SDAI), and ACR/EULAR Boolean remission rates at weeks 2, 4, 8, 12, 24, and 52. QoL was assessed using the Disability Index (HAQ-DI) [16], 36-item Short Form Health Survey (SF-36) [17, 18], and Euro Quality of Life – 5 dimensions and 5 levels (EQ-5D-5L) [19] questionnaires at baseline and weeks 2, 4, 8, 12, 24, and 52 (HAQ-DI only at weeks 2, 4, and 8).

Antidrug antibodies (ADAs) and neutralizing antibodies (NAbs) were assessed at baseline and at scheduled visits at weeks 2, 4, 12, 24, 36, and 52. Blood samples were taken pre-dose and serum concentrations were quantified using a validated enzyme-linked immunosorbent assay. The incidence of ADAs was assessed using a highly sensitive and drug-tolerant validated bioanalytical method based on the Meso Scale Discovery Electrochemiluminescent platform (Meso Scale Diagnostics, Rockville, MD, USA). The assay sensitivity was 86.4 ng/mL with a drug tolerance of 250 μg/mL at the low positive control level of 129.6 ng/mL. In addition, all patients had blood samples taken for population pharmacokinetic (PK) assessment pre-first dose, and then prior to dosing on weeks 2, 4, 12, 24, 36, and 52.

Secondary safety endpoints included the incidence of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) up to week 52 and at the 4-month safety follow-up. Injection site pain was evaluated using a 0–100 visual analogue scale (VAS) after 3 consecutive administrations of study drug (weeks 4, 6, and 8). Pain was evaluated immediately post-injection, and at 15 min and 1 h post-injection.

The primary endpoint was evaluated using the safety analysis set, which consisted of all randomized patients who received at least one dose of study drug. The incidence of treatment-emergent AESIs and 95% CIs were calculated for each treatment group. 95% CIs for the difference in incidence between groups were also calculated for any observed clinical events of AESIs (hypersensitivity) observed in ≥ 3% of patients. Therefore, the study was descriptive, and a sample size of approximately 260 patients was chosen to ensure at least 100 patients remained in each treatment arm at week 52. According to scientific advice from the European Medicines Agency, this sample size is informative for a study primarily focusing on safety in a biosimilar setting [20]. As such, this study was not powered to demonstrate equivalence between MSB11022 and reference adalimumab, and there was no hypothesis tested to justify the sample size.

For the key secondary endpoint, ACR20 at week 12, 95% CIs were calculated for each treatment group. This analysis was performed in both the per-protocol (PP; all randomized and treated patients without important protocol deviations) and intention-to-treat (ITT; all randomized patients) sets. Other secondary endpoints, including efficacy and QoL endpoints, were assessed using the PP and ITT sets, and were summarized descriptively according to the type of outcome. Immunogenicity and safety data, including injection site pain, were summarized descriptively using the safety analysis set. PK data were summarized using the PK analysis set. Analyses exploring associations between PK and immunogenicity and between PK and efficacy also used the PK analysis set.

A total of 288 patients were randomized (ITT: MSB11022, n = 143; reference adalimumab, n = 145). (Fig. 1). All randomized patients received at least one dose of study drug and were included in the safety analysis set. Seven patients (4.9%) in the MSB11022 arm and 12 patients (8.3%) in the reference adalimumab arm were excluded from the PP analysis (PP: MSB11022, n = 136; reference adalimumab, n = 133). Reasons for exclusion from the PP set included being assigned to an incorrect randomization stratum with respect to systemic therapy previously received, using prohibited medication(s) and/or therapies at any time during the study, being < 80% compliant to subcutaneous injection administration, ACR20 could not be calculated at week 12, compliance was below 80% up to week 10, and discontinuing treatment before week 12. Patient demographics and baseline characteristics were similar between treatment arms (Table 1). In both treatment arms, the median number of injections was 25 and the median duration of exposure was 50 weeks.

Few treatment-emergent AESIs of hypersensitivity were reported during the study. The proportions of patients who experienced ≥ 1 hypersensitivity AESI by week 52 was similar across treatment arms: 6 patients (4.2%; 95% CI 1.56, 8.91) in the MSB11022 arm and 8 patients (5.5%; 95% CI 2.41, 10.58) in the reference adalimumab arm (Fig. 2). The types of hypersensitivity reactions recorded were comparable between treatment arms (Table 2). Two hypersensitivity reactions qualified as SAEs: one event of dermatitis (grade 3) in the reference adalimumab arm, and one anaphylactic reaction (grade 4) in the MSB11022 arm, which was considered to be treatment-related. Both events occurred after the completion of the study treatment. The first patient was hospitalized with a generalized erythematous exfoliating dermatitis of the whole body with scalp involvement and secondary superinfection. After 10 days of treatment, the subject was discharged from hospital with significant resorption of the lesions with no new eruptions and improvement of pruritus-related symptoms. The second patient experienced dyspnea, dizziness, vertigo, and nausea 30 min after administration of last study dose of MSB11022. The event resolved with treatment (chloropyramine and methylprednisolone). No subjects permanently discontinued treatment or withdrew from the study due to hypersensitivity, and there were no deaths reported subsequent to a hypersensitivity reaction.

During the 52-week treatment period, 80.4% and 71.7% of patients in the MSB11022 and reference adalimumab treatment arms had at least one positive ADA result, and 39.9% and 39.3% of patients in the MSB11022 and reference adalimumab arms, respectively, had a positive NAb result (Fig. 4). At week 12, the mean (SD) adalimumab trough level for MSB11022 and reference adalimumab was 8,490 (2,291) ng/mL and 7,570 (3,169) ng/mL, respectively, in ADA-negative patients, and 5,070 (3,657) ng/mL and 5,050 (3,514) ng/mL, respectively, in ADA-positive patients. No meaningful differences in ACR20 response rates were reported at scheduled visits up to week 52 when looking separately at ADA-positive and ADA-negative status (Online Resource 6a).

For MSB11022 and reference adalimumab, the mean trough serum concentrations at week 24 were 6,380 ng/mL and 6,550 ng/mL, and at week 52, these were 5,610 ng/mL and 5,330 ng/mL, respectively, with similar concentrations across groups at all time points up to week 52. The presence of ADA had an impact on adalimumab trough concentrations, where ADA-positive subjects had lower trough concentrations compared with ADA-negative subjects; this trend was similar for both MSB11022 and reference adalimumab (Online Resource 6b). The influence of ADA on PK parameters was similar across treatment groups. Lower mean trough concentrations were also observed in the ADA-positive subjects who tested NAb-positive compared with those who tested NAb-negative (data not shown).

The incidence of TEAEs up to week 52 was similar between the treatment arms (MSB11022: n = 83 [58.0%]; reference adalimumab: n = 93 [64.1%]; Table 2. A lower proportion of patients in the MSB11022 compared with the reference adalimumab treatment arm permanently discontinued treatment due to TEAEs (4.2% vs 9.7%). In the 4-month safety follow-up, only 6 patients in each arm experienced a TEAE; none of which were considered to be treatment-related. Few patients experienced an SAE during the treatment period or during the 4-month safety follow-up (Table 2). There was no notable imbalance between the treatment arms.

There were three deaths reported in the study. One patient died of unknown causes prior to randomization. One patient died in the reference adalimumab arm during the treatment period following arteriosclerosis in the coronary artery and myocardial ischemia; this was considered to be unrelated to the treatment. One patient died of unknown causes in the reference adalimumab arm during the 4-month safety follow-up. This was also considered to be unrelated to the treatment.

Fewer injection site reactions (ISRs) were reported in the MSB11022 arm compared with the reference adalimumab arm, 13 patients (9.1%) reported 56 ISRs with MSB11022 and 33 patients (22.8%) reported 298 ISRs with reference adalimumab. A large proportion of reported ISRs concentrated on a small number of subjects experiencing multiple repeat ISRs. The most commonly reported ISRs were erythema, pruritus, and pain, which accounted for more than half of all reported events.

There was no notable pattern in terms of AESIs, TEAEs, or ISRs between the treatment arms with regard to ADA status or NAb status.