Development of biologics active against Th17 pathway targets
Biologic agent | Developer | Psoriasis | PsA | AS | RA | IBD | Other indications |
Anti-IL-17A mAb | |||||||
Secukinumab [AIN457, KB03303A] (Consentyx) | Novartis | Marketed | Marketed | Marketed | P-III | Discontinued (CD) | Alopecia areata (P-II) Atopic dermatitis (P-II) |
Ixekizumab [LY2439821] (Taltz) | Eli Lily | Marketed | P-III (submitted) | P-III | P-II | ||
CNTO 6785 | Janssen, MorphoSys | P-II | COPD (P-II) | ||||
CJM112 | Novartis | P-I/II | Acne (P-II) Hydradenitis suppurativa (P-II) | ||||
BCD 085 | Biocad | P-II | P-II | ||||
SCH-900117 | Merck & Co | P-I | |||||
Perakizumab [RG 4934, RO 5310074] | Roche | Discontinued | |||||
Dual anti-IL-17A and anti-IL-17F mAb | |||||||
Bimekizumab [CDP-4940, UCB-4940] | UCB | P-II | P-II | P-II | P-II | P-II (UC) | |
ALX-0761 [MSB-0010841, M-1095] | Merck Serono, Ablynx | P-I | |||||
RG 7624 [NI-1401, MCAF-5352A] | Genentech, NovImmune SA | Preclinical | |||||
Dual IL-17A and TNF-α mAb | |||||||
ABT-122 | AbbVie | P-II | P-II | ||||
COVA322 | Janssen | P-I/II | |||||
ABBV-257 | AbbVie | P-I | |||||
LY 3114062* | Eli Lilly | ‘Inflammatory arthritis’ (P-I) | |||||
Anti-IL-17RA mAb | |||||||
Brodalumab [AMG 827, KHK4827] (Lumicef, Siliq, Kyntheum) | AstraZeneca, Kyowa Hakko Kirin, Valeant Pharmaceuticals, LEO Pharma | Marketed | Marketed† | P-III | Discontinued | Discontinued (CD) | |
Anti-IL-12/23p40 mAb | |||||||
Ustekinumab [CNTO-1275] (Stelara) | Janssen | Marketed | Marketed | P-III | Discontinued | Marketed (CD) P-III (UC) | SLE (P-II) Atopic dermatitis (P-II) |
Briakinumab [ABT-874, A-796874.0, BSF415977, J695, LU415977, WAY-165772] (Ozespa) | Abbott | P-III (submission withdrawn) | Discontinued | Discontinued (CD) | |||
Anti-IL-23 mAb | |||||||
Guselkumab [CNTO-1959] | Janssen, MorphoSys | P-III (submitted) | P-II | P-II | |||
Tildrakizumab [SCH-900222, MK-3222] | Merck, Sun Pharmaceutical Industries | P-III (submitted) | P-II | P-II | |||
Brazikumab [AMG 139, MEDI2070] | Allergan, AstraZeneca, Amgen | P-II (CD) | |||||
Risankizumab [ABBV 066, BI 655066] | Boehringer Ingelheim, AbbVie | P-III | P-II | P-II | P-II (CD) | Asthma (P-II) | |
Mirikizumab [LY 3074828] | Eli Lilly | P-II | P-II (CD and UC) |
Adapted from Refs 4 6 122 123. Development status based on http://adisinsight.springer.com, accessed 30 May 2017.
*LY3114062 mechanism of action is not yet disclosed, but believed to be a dual IL-17/TNF-α inhibitor.
†Brodalumab approved for treatment of psoriatic arthritis in Japan, although currently not approved for this indication in USA or Europe.
AS, ankylosing spondylitis; CD, Crohn’s disease; COPD, chronic obstructive pulmonary disease; IBD. inflammatory bowel disease; IL, interleukin; P-I, phase I clinical trial; P-II, phase II clinical trial; P-III, phase III clinical trial; PsA, psoriatic arthritis; mAb, monoclonal antibody; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus; Th, T-helper; TNF, tumour necrosis factor; UC, ulcerative colitis.