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[Disclosure] Celltrion (068270) – Approval of Korean MFDS Marketing Authorization for Avtozma Subcutaneous Injection (CT-P47, Actemra Biosimilar) / 2025-02-13

Posted on February 13, 2025August 6, 2026 By K-STOCK Editor

Fact Source: Financial Supervisory Service DART

💡 3-Second Summary

Celltrion received marketing authorization from the Ministry of Food and Drug Safety (MFDS) of South Korea for Avtozma Subcutaneous Injection (CT-P47), a biosimilar referencing Actemra, for the treatment of rheumatoid arthritis.

📊 Key Disclosure Content & Financial Highlights

  1. Overview
  • Company: Celltrion, Inc. (Stock Code: 068270)
  • Disclosure Type: Major Matters Report Related to Investment Decisions
  • Subject: Korean MFDS Marketing Authorization Approval for Avtozma Subcutaneous Injection (CT-P47, Actemra Biosimilar)
  • Regulatory Authority: Ministry of Food and Drug Safety (MFDS), South Korea
  • Key Dates:
    • Application Date: 2024-02-28
    • Marketing Approval Date: 2025-02-12
  • Confirmation Date: 2025-02-12 (Date MFDS approval was confirmed)
  1. Product & Indication Details
  • Approved Product: Avtozma Subcutaneous Injection (CT-P47, Active Ingredient: Tocilizumab)
  • Approved Indication: Rheumatoid arthritis
  1. Key Details & Future Plans
  • Approval Details: Secured domestic marketing authorization for Avtozma Subcutaneous Injection for the specified target indication
  • Expected Effects: Expanded therapeutic options for patients in South Korea suffering from rheumatoid arthritis
  • Additional Notes: Content will be utilized in upcoming press releases and IR materials

📝 Editor’s Comment (Key Follow-up Checkpoint)

📌 Verification of Domestic Marketing Authorization Listing in Official Documents

This disclosure serves as official notification regarding MFDS marketing approval for Avtozma Subcutaneous Injection in South Korea. Checking whether the marketing authorization status is accurately reflected in the company’s official periodic reporting documents is important for verifying the formal regulatory documentation. Relevant updates can be confirmed through subsequent periodic reports or official IR materials.

📢 Disclaimer & Source Notice

Source: This content was structured and generated based on official disclosure data from the Financial Supervisory Service’s DART system.

Investment Risk Warning: This material is provided for informational and language reference purposes only. Under no circumstances does it constitute financial advice or a recommendation to buy or sell specific stocks. All investment decisions and financial responsibilities rest solely with the investor.

Contact: For compliance inquiries or copyright requests, please contact ksb220805@gmail.com.

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