Lilly breakthrough: Dual treatment clears skin & cuts weight in psoriasis patients
The trial targeted a patient population with high BMI and extensive skin involvement, averaging over 39 kg/m²
The trial targeted a patient population with high BMI and extensive skin involvement, averaging over 39 kg/m²
The therapy was well tolerated through Week 24, with a safety profile consistent with Alumis’ Phase 2 data
The filing clears the regulatory path for potential first-in-human trials and marks a key advance in the company’s chronic inflammatory disease pipeline
Takeda said zasocitinib was generally well tolerated, with a safety profile consistent with earlier studies
Imsidolimab, an IgG4 IL-36 receptor antagonist, works by inhibiting IL-36 receptor signaling, directly addressing the deficiency in the IL-36RA regulator common in GPP patients
Ilumya is the first IL-23 inhibitor to complete five years of study based on a pooled analysis of two Phase 3 efficacy and safety extension trials
The study demonstrated equivalent efficacy, safety, immunogenicity, and pharmacokinetics between YESINTEK and the reference product Stelara
The drug exhibited greater treatment persistence and control of moderate-to-severe PsO symptoms compared to secukinumab and ixekizumab
EC grants conditional marketing authorization based on the EFFISAYIL trial
CHMP positive opinion is based on evidence from the EFFISAYIL trial, the largest clinical trial in
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