AURIEL-PsO: a randomized, double-blind phase III equivalence trial to demonstrate the clinical similarity of the proposed biosimilar MSB11022 to reference adalimumab in patients with moderate-to-severe chronic plaque-type psoriasis.
J HercogováKim A PappV ChyrokM UllmannP VlachosC J EdwardsPublished in: The British journal of dermatology (2019)
Therapeutic equivalence between MSB11022 and reference adalimumab was demonstrated. AURIEL-PsO provides evidence to support the similarity of both products with regard to efficacy, safety and immunogenicity. What's already known about this topic? Adalimumab is a fully human antitumour necrosis factor-α monoclonal antibody, indicated for the treatment of multiple inflammatory disorders, including psoriasis, psoriatic arthritis, rheumatoid arthritis, inflammatory bowel diseases and ankylosing spondylitis. MSB11022 is a proposed adalimumab biosimilar that has shown structural and functional similarity to the reference product in an extensive analytical comparability exercise. MSB11022 has demonstrated bioequivalence and comparable safety and immunogenicity profiles in a phase I study in healthy volunteers. What does this study add? This phase III study confirmed equivalent efficacy for MSB11022 and reference adalimumab in patients without any immunomodulation comedication in moderate-to-severe chronic plaque-type psoriasis at week 16. The efficacy, safety and immunogenicity of MSB11022 and reference adalimumab were similar over the respective observation periods (week 52 for efficacy and immunogenicity, week 66 for safety). A switch from reference adalimumab to MSB11022 at week 16 did not impact efficacy, safety or immunogenicity.
Keyphrases
- rheumatoid arthritis
- phase iii
- ankylosing spondylitis
- placebo controlled
- double blind
- juvenile idiopathic arthritis
- clinical trial
- disease activity
- open label
- hidradenitis suppurativa
- ulcerative colitis
- end stage renal disease
- chronic kidney disease
- coronary artery disease
- randomized controlled trial
- endothelial cells
- peritoneal dialysis
- drug induced
- systemic lupus erythematosus
- atopic dermatitis
- oxidative stress
- systemic sclerosis
- liquid chromatography
- pluripotent stem cells