Press Releases

03-06 Celltrion to expand treasury share cancellation to 9.11 million shares: Prioritizing shareholder value amid heightened market uncertainty PU
02-19 Celltrion : New ECCO data show subcutaneous (SC) infliximab (Remsima™ SC) effectively recaptures and maintains disease control after drug holiday PU
02-12 Celltrion : to Submit Approx KRW 1.46Tn Treasury Share Cancellation Proposal to Shareholders’ Meeting; To Amend Articles Ahead of Commercial Act Revision to Enhance Transparency and Shareholder Value PU
02-05 Celltrion : Reports Record-High Annual Revenue of KRW 4.1625Tn and Operating Profit of KRW 1.1685Tn in 2025… Signaling Continued Strong Growth Backed by High-Margin Newer Portfolio PU
01-08 Celltrion And Sandoz Launch Their Aflibercept Biosimilars In Europe AQ
11-05 FDA Grants Interchangeability Designation To Fresenius Kabi's And Celltrion's Denosumab Biosimilars AQ
14/10/25 Celltrion Announces Launch Of AVTOZMA® (Tocilizumab-anoh) Intravenous Formulation In The United States AQ
30/09/25 FDA Approves Biocon's Denosumab Biosimilars AQ
16/06/25 Celltrion : announces U.S. FDA approval of additional presentation of STEQEYMA® (ustekinumab-stba), expanding dosing options for pediatric patients PU
12/05/25 Celltrion : Investor Presentation May & June 2025 PU
29/04/25 Celltrion Adalimumab Biosimilar Granted Interchangeability Designation AQ
28/03/25 Celltrion's STEQEYMA, now added to the Costco Member Prescription Program AQ
28/03/25 Celltrion Wins Costco Formulary Listing For Its Recently Launched Ustekinumab AQ
26/03/25 Celltrion Launches STEQEYMA® (ustekinumab-stba) In The United States AQ
10/03/25 U.S. FDA approves Celltrion's OMLYCLO as the first and only biosimilar with interchangeability designation referencing XOLAIR AQ
06/03/25 Celltrion : Investor Presentation March & April 2025 PU
25/02/25 Celltrion : FY2024, 4Q24 Earning Release Celltrion Inc. PU
24/02/25 Celltrion Receives EC Approval for Avtozma, a Biosimilar to RoActemra AQ
31/01/25 Amgen And Celltrion Settle Denosumab BPCIA Case AQ
09/01/25 FDA Approves Celltrion's STEQEYMA (Ustekinumab-stba) AQ
21/11/24 BPCIA Lawsuit Against Accord's Proposed Prolia® / Xgeva® Biosimilar Filed By Amgen AQ
07/11/24 FDA Accepts ABLAs For Prolia® / Xgeva® Biosimilars From Organon And Teva AQ
16/10/24 Celltrion presents 2-year post-hoc analysis findings for subcutaneous infliximab, highlighting dose escalation as an option for managing loss of response in inflammatory bowel disease AQ
16/10/24 Amgen Files BPCIA Complaint Against Fresenius Kabi Regarding Denosumab AQ
20/09/24 Celltrion Wins Brazilian Federal Tender For Trastuzumab For Fifth Consecutive Year AQ
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