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[Disclosure] Celltrion (068270) – Approval of Phase 3 Clinical Trial Plan in Korea for CT-P44 (Darzalex Biosimilar) / 2025-07-03

Posted on July 3, 2025August 6, 2026 By K-STOCK Editor No Comments on [Disclosure] Celltrion (068270) – Approval of Phase 3 Clinical Trial Plan in Korea for CT-P44 (Darzalex Biosimilar) / 2025-07-03

Fact Source: Financial Supervisory Service DART

💡 3-Second Summary

Celltrion has received Phase 3 Clinical Trial Application (IND) approval from the Ministry of Food and Drug Safety (MFDS) of Korea for ‘CT-P44’, a biosimilar candidate to Darzalex, enabling patient recruitment and clinical trial execution in South Korea.

📊 [Key Disclosure Details & Financial Summary]

  • Disclosure Title: Approval of Phase 3 Clinical Trial Plan in Korea for CT-P44 (Darzalex Biosimilar)
  • Target Product: CT-P44 (Biosimilar to Darzalex / Darzalex Faspro, Subcutaneous Injection)
  • Clinical Trial Phase: Global Phase 3 Clinical Trial
  • Target Indication: Refractory or Relapsed Multiple Myeloma
  • Filing & Approval Dates (Regulatory Authority):
    • IND Application Date: March 20, 2025
    • Approval Date: July 2, 2025 (Fact Confirmation Date: July 2, 2025)
    • Regulatory Authority: Ministry of Food and Drug Safety (MFDS), Korea / EU CT Number: 2024-518588-36-00
  • Trial Design & Scale:
    • Number of Subjects: 486 patients
    • Trial Period: Approx. 2 years
    • Trial Design: Double-blind, randomized, active-controlled, parallel-group Phase 3 trial (in combination with lenalidomide and dexamethasone)
  • Purpose & Future Plans:
    • Demonstrating biosimilarity in terms of efficacy and safety compared to the reference drug Darzalex
  • Investment Caution:
    • Statistically, the average success rate for clinical-stage drugs reaching final regulatory approval is around 10%

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

📌 Verification of Domestic Clinical Site Activation and First-Patient Dosing Progress

This disclosure confirms that Celltrion has secured IND approval from the Korean MFDS for Phase 3 clinical trials of CT-P44. Following regulatory clearance, it is key to monitor the initiation of patient recruitment and first-patient dosing (FPD) at Korean clinical sites. Tracking subject enrollment and execution of the planned 2-year R&D timeline confirms operational development progress. Clinical progress and enrollment milestones can be verified through future regulatory filings or upcoming periodic reports (Quarterly, Half-Yearly, or Annual Business Reports).

📢 Disclaimer & Source Information

Source: This content was newly generated and structured based on official data submitted to the Data Analysis, Retrieval and Transfer System (DART) of the Financial Supervisory Service.

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

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

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