Pfizer Reports Results of Abrocitinib in P-III JADE MONO-2 Study for Moderate to Severe Atopic Dermatitis

Pfizer Reports Results of PF-05280586 (rituximab biosimilar) in REFLECTIONS B328-06 study for CD20-Positive Non-Hodgkin Lymphoma


  • The P-III JADE MONO-2 study involves assessing of Abrocitinib (qd, 100mg & 200mg) vs PBO in 391 patients with mod. to sev. AD aged ≥12yrs. for 12wks.
  • The P-III JADE MONO-2 study results: met its 1EPs & 2EPs i.e, improvement in IGA score of clear (0) or almost clear (1) skin, ≥75% change in baseline in EASI score & 4point or larger reduction in itching measured with a decrease in magnitude in PSAAD respectively, safety results are consistent with JADE MONO-1 study
  • Abrocitinib is an oral JAK-inhibitor, modulating multiple cytokines involved in the pathophysiology of AD, including IL-4, IL-13, IL-31, and interferon-gamma and has received FDA’s BT designation in Feb’2018

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