AstraZeneca’s Tezepelumab (thymic stromal lymphopoietin antagonist) Receives FDA BT Designation for the Treatment of Severe Asthma with irrespective T2 biomarker status

 AstraZeneca’s Tezepelumab (thymic stromal lymphopoietin antagonist) Receives FDA BT Designation for the Treatment of Severe Asthma with irrespective T2 biomarker status

AstraZeneca’s Tezepelumab (thymic stromal lymphopoietin antagonist) Receives FDA BT Designation for the Treatment of Severe Asthma with irrespective T2 biomarker status

Shots:

  •  The designation is based on P-IIb PATHWAY assessing (tezepelumab vs PBO) in patients with asthma exacerbations, uncontrolled asthma receiving inhaled corticosteroids/LA- β2-agonists w/o oral corticosteroids and additional asthma controllers
  •  P-IIb PATHWAY involves administering of (70/210mg q4w or 280mg q2w) which showed reduction in annual asthma exacerbation rate reductions of 62%, 71% and 66% vs PBO
  • AZ received seven BT designation since 2014, with first in respiratory and tezepelumab is under P-III PATHFINDER clinical trial programme

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Vartika Singh

Vartika Singh is a content writer who loves to write research articles and reports at PharmaShots. She has in-depth knowledge of the life sciences industry including the Pharma and Biotech sectors. Any articles written by her can be contacted at connect@pharmashots.com.

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