Logo

The EMA Accepts Formycon’s MAA for FYB203 to Treat Neovascular Age-Related Macular Degeneration (AMD)

Share this
Formycon

The EMA Accepts Formycon’s MAA for FYB203 to Treat Neovascular Age-Related Macular Degeneration (AMD)

Shots: 

  • Formycon and its license partner Klinge Biopharma have received the EMA’s acceptance on the MAA submitted for FYB203 (biosimilar Eylea) for the treatment of AMD  
  • Eylea is a long-acting injectable form of aflibercept prescribed to be administered q2month or q4month after the initial dosing period for the treatment of neovascular wet AMD or other retinal diseases
  • The company had previously launched Ranivision (FYB201, biosimilar ranibizumab) for the treatment of neovascular AMD and other retinal diseases in EU 

Ref: FORMYCON | Image: FORMYCON

Related News:- Formycon and its License Partner Klinge Biopharma Reports the BLA Submission of FYB203 (Biosimilar, Eylea) to the EMA

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 

Shivani Chandra

Shivani was a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She was covering news related to Product approvals, clinical trial results, and updates. We 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