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Rapid pruritus reduction with ruxolitinib cream treatment in patients with atopic dermatitis.
Blauvelt, Andrew; Kircik, Leon; Papp, Kim A; Simpson, Eric L; Silverberg, Jonathan I; Kim, Brian S; Kwatra, Shawn G; Kuligowski, Michael E; Venturanza, May E; Wei, Shaoceng; Szepietowski, Jacek C.
Afiliación
  • Blauvelt A; Oregon Medical Research Center, Portland, Oregon, USA.
  • Kircik L; Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Papp KA; K. Papp Clinical Research and Probity Medical Research, Waterloo, Ontario, Canada.
  • Simpson EL; Oregon Health & Science University, Portland, Oregon, USA.
  • Silverberg JI; George Washington University, Washington, District of Columbia, USA.
  • Kim BS; Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Kwatra SG; Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Kuligowski ME; Incyte Corporation, Wilmington, Delaware, USA.
  • Venturanza ME; Incyte Corporation, Wilmington, Delaware, USA.
  • Wei S; Incyte Corporation, Wilmington, Delaware, USA.
  • Szepietowski JC; Department of Dermatology, Venereology, and Allergology, Wroclaw Medical University, Wroclaw, Poland.
J Eur Acad Dermatol Venereol ; 37(1): 137-146, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36066323
BACKGROUND: Ruxolitinib cream is a topical formulation of ruxolitinib, a Janus kinase (JAK) 1/JAK2 inhibitor. OBJECTIVES: To report timing and magnitude of effect of ruxolitinib cream on itch in patients with atopic dermatitis (AD), a highly pruritic inflammatory skin disease. METHODS: Two phase 3 trials (TRuE-AD1 [NCT03745638]/TRuE-AD2 [NCT03745651]) enrolled patients aged ≥12 years with AD for ≥2 years, Investigator's Global Assessment score of 2 or 3, and 3%-20% affected body surface area. Patients (total N = 1249; median age, 32 years) were randomised (2:2:1) to twice daily 0.75% ruxolitinib cream, 1.5% ruxolitinib cream or vehicle cream for 8 weeks of double-blinded treatment. Worst itch was measured using the numerical rating scale (NRS). RESULTS: Significantly more patients who applied ruxolitinib cream (either strength) achieved a ≥2-point itch reduction (NRS2) within approximately 12 h versus vehicle (0.75%/1.5% ruxolitinib cream, 16.3%/13.1%; vehicle, 6.9%; both P < 0.05), with further improvements through Week 8 (58.3%/65.1% vs 29.4%; both P < 0.0001). A ≥4-point itch reduction (NRS4) was achieved by significantly more patients who applied 0.75%/1.5% ruxolitinib cream versus vehicle by Day 2 (8.9%/11.2% vs 2.1%; P < 0.005); higher rates were observed at Week 8 (41.5%/51.5% vs 15.8%; P < 0.0001). Median time for the 0.75%/1.5% ruxolitinib cream groups to achieve NRS4 from baseline was 15.0/13.0 days; this endpoint was not reached by the vehicle group. CONCLUSIONS: Ruxolitinib cream demonstrated rapid improvement in itch in patients with mild to moderate AD that was sustained for 8 weeks. Significantly more patients applying ruxolitinib cream achieved itch NRS2 within approximately 12 h and itch NRS4 by Day 2 versus vehicle.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dermatitis Atópica / Inhibidores de las Cinasas Janus Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dermatitis Atópica / Inhibidores de las Cinasas Janus Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos