InnoCare Pharma Ltd. has received regulatory approval from the Center for Drug Evaluation $(CDE)$ to conduct a phase III registrational clinical trial of orelabrutinib for the treatment of systemic lupus erythematosus $(SLE)$. This approval follows the successful achievement of the primary endpoint in the phase IIb study, where orelabrutinib demonstrated outstanding efficacy and a well-tolerated safety profile in SLE patients.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. InnoCare Pharma Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9601891-en) on December 14, 2025, and is solely responsible for the information contained therein.
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