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Biocon Reports P-I Study (RHINE-3) Results of Biosimilar Insulin

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Biocon Reports P-I Study (RHINE-3) Results of Biosimilar Insulin

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  • The P-I study (RHINE-3) evaluating a single dose of 0.4IU/kg of Biocon's Insulin-70/30 vs US-licensed Humulin-70/30 vs in a ratio (1:1) in 78 patients
  • The results showed a PK & PD equivalence b/w the biosimilar insulin-70/30 and Humulin-70/30 as a single SC administration for the primary EPs. The study also showed equivalence for the secondary PK/PD EPs & was well-tolerated with no clinically relevant differences in the safety profiles & no serious AEs were reported
  • Additionally, plasma insulin concentrations and glucose infusion rates (GIRs) were assessed over 24hrs., no serious AEs, deaths, or discontinuations due to safety or tolerability reasons were reported

Ref: CrenterforBiosimilar Image: Biocon

Related News:- Lannett Entered into a Patent License Agreement with Ypsomed and HEC for Pen Injector Device in Use of Biosimilar Insulin Glargine and Insulin Aspart

Click here to­ read the full press release 

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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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