Pfizer Reports Results of Abrocitinib in Fifth P-lll JADE REGIMEN Across Different Dosing Regimens
Shots:
- The P-lll JADE REGIMEN study involves assessing of Abrocitinib (100/ 200mg) vs PBO in 1233 patients aged ≥ 12 yrs. in a ratio (1:1:1) with mod. to sev. AD following response to initial open-label induction treatment with abrocitinib (200mg)
- Result: The study met its 1EPs i.e. probability of not experiencing a flare @52wks. (81.1%- 57.4% vs 19.1%) and 2EPs i.e. patients maintain an IGA response of clear or almost clear relative
- Following an initial 12wks. induction treatment phase- fewer patients experienced a flare at any point in the trial @40wks. Abrocitinib is a JAK inhibitor- which modulates multiple cytokines involved in the pathophysiology of AD- including IL-4- IL-13- IL-31- IL-22- and TSLP
Ref: Pfizer | Image: Forbes
Click here to read the full press release
Tags
This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com