Switzerland-based Novartis has revealed new data for 441 Chinese patients with moderate to severe plaque psoriasis from a Phase III study investigating the efficacy and safety of its psoriasis drug, Cosentyx (secukinumab), it was reported yesterday.
The data is a part of a broader ongoing 52 week Phase III study in 543 patients, indicating 97.7% of patients treated with Cosentyx 300mg achieved PASI 75 and 80.9% achieved PASI 90 by week 12, with 87% of patients reaching PASI 90 by week 16. In patients treated with Cosentyx 150mg, 87.8% achieved PASI 75 and 66.4% achieved PASI 90 at week 12.
Novartis says that Cosentyx is backed by a wealth of research with 100 studies and has been proven to offer clear or almost clear skin in 8 out of 10 patients within 16 weeks of treatment. The product is a targeted biologic and the first and only fully-human treatment that specifically inhibits IL-17A, a cornerstone cytokine involved in the inflammation and development of psoriatic disease, including psoriasis, psoriatic arthritis and ankylosing spondylitis.
Celltrion launches AVTOZMA IV in the United States following FDA approval
Novartis to launch US direct-to-patient platform for Cosentyx
Vascarta completes VAS-101 osteoarthritis clinical trial
Sen-Jam Pharmaceutical and KVK Tech complete final development deliverables for SJP-002C
OSE Immunotherapeutics forms strategic alliance with Inserm Transfert and Nantes University
ResVita Bio completes face-to-face Pre-IND meeting with FDA for RVB-003
N4 Pharma advances RNA delivery breakthrough with SRI collaboration
EMA recommends marketing approval of Alvotech's Gobivaz biosimilar to Simponi
Evommune reveals further positive data from Phase 2 EVO756 trial
J & D Pharmaceuticals receives Orphan Drug Designation for JD-004
Ascletis presents Phase III results of denifanstat (ASC40) for acne treatment at EADV Congress 2025
Sanofi reports positive phase 2a results for brivekimig in hidradenitis suppurativa