Logo

Formycon and Fresenius Kabi Settled with Johnson & Johnson for FYB202, a Proposed Biosimilar to Stelara (ustekinumab)

Share this
Formycon

Formycon and Fresenius Kabi Settled with Johnson & Johnson for FYB202, a Proposed Biosimilar to Stelara (ustekinumab)

Shots:

  • Formycon and Fresenius Kabi entered into a settlement agreement with Johnson & Johnson concerning FYB202, a proposed ustekinumab biosimilar in the US. FYB202 can be marketed in the US subject to regulatory approval, no later than April 2025
  • FYB202, a human mAb that targets the cytokines interleukin-12 and interleukin 23 for immune-mediated disorders. Stelara was approved for mod. to sev. PsO, CD, UCas well as active PsA
  • Formycon seeks to submit the BLA in 2023. Formycon & Fresenius Kabi collaborated in Feb 2023 to commercialize the proposed ustekinumab biosimilar (FYB202) in key global markets after successful approvals while both companies share equal post-commercialization value

Ref: FORMYCON | Image: FORMYCON

Related News:- Formycon AG and its License Partner Klinge Biopharma GmbH Report the BLA Submission of FYB203 (biosimilar, aflibercept) to the US FDA

PharmaShots! Your go-to media platform for customized news ranging for multiple indications. For more information connect with us at connect@pharmashots.com

Click here to­ read the full press release 

Senior Editor

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.

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions