医療従事者の為の最新医療ニュースや様々な情報・ツールを提供する医療総合サイト

Celltrion Enters into Phases 1 and 3 Clinical Trials for the Adalimumab Biosimilar ‘CT-P17′

2018年08月07日 PM08:55
このエントリーをはてなブックマークに追加


 

INCHEON, South Korea

Celltrion (KRX:068270) applied for the clinical trials for its adalimumab biosimilar ‘CT-P17’, as a rheumatoid arthritis therapeutic agent, to the MHRA (Medicines and Healthcare Products Regulatory Agency) in the UK.

Celltrion is set to launch phase 1 clinical trials for the safety and pharmacokinetic assessment of the adalimumab biosimilar in the UK. And Celltrion also conducts global phase 3 clinical trials in about 75 sites in eight nations in European region from August 2018. It aims to complete phase 3 clinical trials by 2020.

The Abbvie’s HUMIRA®, the original medicine of CT-P17, is a therapeutic biopharmaceutical for the treatment of rheumatoid arthritis, inflammatory bowel disease, psoriatic arthritis, ankylosing spondylitis, etc., and it recorded sales of about USD 18.4 billion in 2017,1 making it the global largest-selling blockbuster medicine.

Celltrion has developed CT-P17 as a high-concentration formulation and thus differentiated it from the competitive biosimilars which are conducting clinical trials or have already been approved.

Meanwhile, after completing clinical trials for CT-P17, Celltrion is set to maximize its market share in TNF-α inhibitor biosimilar markets under the strategy of diversifying its TNF-α inhibitors along with Remsima®, already sharing 52%2 of the Europe’s original medicine market, and CT-P13 SC which is undergoing clinical trials with the goal of obtaining approvals in 2019.

1 Abbvie 2017 Annual Report
2 IQVIA 2017 data

About Celltrion, Inc.

Headquartered in Incheon, Korea, Celltrion is a leading biopharmaceutical company, specializing in research, development and manufacture of biosimilar and innovative drugs. Celltrion strives to provide more affordable biosimilar mAbs to patients who previously had limited access to advanced therapeutics. Celltrion received FDA and EC’s approval for INFLECTRA® and Remsima®, respectively, which is the world’s first mAb biosimilar to receive approval from a regulatory agency in a developed country. For more information, visit www.celltrion.com.

View source version on businesswire.com: https://www.businesswire.com/news/home/20180807005445/en/

CONTACT

Celltrion, Inc.
Gunn Lee, +82-32-850-5168
Gunhyuk.lee@celltrion.com
or
Heewon
Park, +82-32-850-5356
Heewon.park@celltrion.com

同じカテゴリーの記事 

  • Shaperon to Conduct Strategic Partnering and Institutional Investor Meetings at the 10th Annual BFC Healthcare Business Development & Investment Conference in Shanghai
  • Makana™ Issued Patent in South Korea for Its Genetically-Modified TKO Pig for Use in Xenotransplantation
  • Aurion Biotech Announces Completion of Enrollment in Phase 1 / 2 Clinical Trial
  • Poxel Provides a Financial Update for the First Quarter 2024 and Announces the Postponement of its 2023 Full-Year Results Release
  • ENHERTU® Demonstrated Statistically Significant and Clinically Meaningful Improvement in Progression-Free Survival in HR Positive, HER2 Low Metastatic Breast Cancer Following One or More Lines of Endocrine Therapy in DESTINY-Breast06 Phase 3 Trial