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FDA approves Yesintek, a biosimilar to the reference product, Stelara – Biocon Biologics

Written by | 7 Dec 2024

Biocon Biologics Ltd , a fully integrated global biosimilars company and subsidiary of Biocon Ltd, announced  that the FDA  has approved Yesintek (ustekinumab-kfce), a biosimilar to the reference… read more.

Skyrizi met all primary and secondary endpoints versus Stelara in head-to-head study in Crohn’s disease – AbbVie

Written by | 16 Sep 2023

AbbVie announced top-line results from the Phase III SEQUENCE clinical trial evaluating risankizumab (Skyrizi, 600 mg intravenous [IV] induction at week 0, 4 and 8 and 360 mg… read more.

Janssen submits application seeking FDA approval of Stelara for the treatment of pediatric patients with juvenile psoriatic arthritis

Written by | 24 Oct 2021

The Janssen Pharmaceutical Companies of Johnson & Johnson announced the submission of a supplemental Biologics License Application (sBLA) to the FDA seeking expanded approval of Stelara (ustekinumab) to… read more.

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