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BioFactura Reports P-I Study Results of BFI-751 (biosimilar, ustekinumab)

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BioFactura

BioFactura Reports P-I Study Results of BFI-751 (biosimilar, ustekinumab)

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  • The P-I study results published in the peer-reviewed journal, Clinical Pharmacology in Drug Development evaluating PK profiles of BFI-751 vs EU & US ustekinumab in 216 healthy adult volunteers
  • All 3 treatments met the standard BE criteria that is CI: 90% of the geometric mean ratios of AUC (0-infinity), AUC (0 to Cmax), and maximum concentration are completely within the acceptance interval
  • No differences in the safety, immunogenicity & tolerability profiles were seen with no difference in the overall incidence of injection site reactions after dosing among treatment groups. BioFactura & CuraTeQ sign exclusive license for BFI-751, a biosimilar to Stelara on July 2023

Ref: Cision PR Web Image: Biofactura

Related News:- Aurobindo Pharma Subsidiary CuraTeQ Signs an Exclusive License Agreement with BioFactura to Commercialize BFI-751, a proposed biosimilar to Stelara

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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