in guidelines
in dermatology and rheumatology
dosing scheme1
Indication in DERMATOLOGY AND RHEUMATOLOGY1:
Within DERMATOLOGY AND RHEUMATOLOGY, Uzpruvo® is approved to treat:1
Uzpruvo® is currently not approved for the ulcerative colitis indication (since the originator still has exclusivity for this indication)
and Paediatric
Plaque Psoriasis
Arthritis
UNIQUE mode of action of ustekinumab:
IL12/IL23-receptor binding inhibition
Ustekinumab is a fully human IgG1κ monoclonal antibody that binds with specificity to the shared p40 protein subunit of pro-inflammatory cytokines IL-12 and IL-23 to prevent them from binding to their receptors, expressed on the surface of immune cells, therefore inhibiting inflammatory processes early1
UZPRUVO® IN DERMATOLOGY & RHEUMATOLOGY
POSOLOGY OPTIONS1
Choose between two dose strengths to suit individual treatment needs
Maintenance:
SC Injection*
Presentation:
Pre-filled Syringe
SC, subcutaneous
Dosing Scheme1
BW, body weight; PFS, pre-filled syringe; Q12W, every 12 weeks; SC, subcutaneous
1. Uzpruvo® SmPC.
Uzpruvo® vs The reference product*:
Phase III Trial Design1
Primary objective: PASI % improvement from BL to Week 12
Secondary objective:
- PASI 50/75/90/100 response rates from BL at Weeks 4, 8, 12, 16, 28, 40 and 52
- PASI % improvement from BL to Weeks 4, 8, 16, 28, 40 and 52
- sPGA responses
- Change from baseline in DLQI and BSA affected by psoriasis
- Additional secondary assessments were safety, serum trough concentrations at steady state and immunogenicity
Adapted from Feldman SR et al. 20231
BL, baseline; BSA, body surface area; DLQI, Dermatology life quality index; EoS, end of study; PASI, Psoriasis Area and Severity Index; Q12W, every 12 weeks; SC, subcutaneous; sPGA, statistic physician's global assessment
*Stelara®; **≤100 kg body weight: 45 mg, >100 kg body weight: 90 mg
1. Feldman SR et al. Expert Opin Biol Ther. 2023;23(3):253-60. DOI: 10.1080/14712598.2023.2235263.
Uzpruvo® vs The reference product*:
Similar safety PROFILE, even after switching1
Comparable AE profiles for Uzpruvo® and the reference product* up to Week 52, even after switching
Adapted from Feldman SR et al. 20231
AE, adverse event; RP, reference product; TEAE, treatment-emergent adverse event
*Stelara® 1. Feldman SR et al. Expert Opin Biol Ther. 2023;23(3):253-60. DOI: 10.1080/14712598.2023.2235263.