As capacity at its 3 existing plants begins to run out, Samsung Biologics will add a fourth plant to its Incheon, Republic of Korea, site.
As Samsung Biologics’ bioreactor facilities are expected to reach full utilization by 2022, the company said it will construct a fourth plant and a bio campus, according to industry reports.
Samsung Biologics and Biogen are major shareholders in the biosimilar manufacturer Samsung Bioepis, which is anticipating the European Commission approval of its bevacizumab biosimilar candidate (Aybintio). The developmental agent was recommended for approval by the European Medicines Agency’s Committee for Medicinal Products for Human Use in June.
Samsung Biologics has seen activities expand at its site in Incheon, Republic of Korea, since it began constructing its first of 3 manufacturing plants there in 2011. The production center has a bioreactor capacity of 364,000 liters, according to The Korea Times, reporting on a recent shareholder meeting.
Recent large-scale contract announcements indicate that excess plant capacity will be used up in 2 years, and Kim Tae-han, CEO of Samsung Biologics, said the need for more production capacity led to the decision to design a fourth plant, according to BioProcess International.
Samsung Biologics’ Deals
Samsung Biologics is a contract and development management organization, meaning that it serves other pharmaceutical companies on a contract basis to provide comprehensive drug development and manufacturing services.
In March, The Korea Times reported that Samsung Biologics will open a research and development lab in the San Francisco, California, area later in 2020, which in terms of physical expansion, marks the company’s first steps outside the Republic of Korea.
According to the Nikkei Asian Review, Samsung Biologics has closed over $1.5 billion worth of orders in the past 3 months.
The Japanese media outlet stated that Samsung Biologics made a deal in April with Vir Biotechnology worth $362 million for Samsung Biologics to help the US-based company initiate production of a coronavirus disease 2019 antibody treatment. Samsung Biologics notched a deal in May valued at $231 million to manufacture biologics, including lupus drug Benlysta (belimumab), for GlaxoSmithKline.
Top 5 Most-Read Oncology Articles of 2024
December 24th 2024The top 5 oncology biosimilar articles in 2024 cover Duke's recommendations for cell and gene therapy biosimilars, FDA approval of Shanghai Henlius Biotech's trastuzumab biosimilar, Boehringer Ingelheim layoffs, the safety of rituximab biosimilar CT-P10, and more.
Biosimilars Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
Review Confirms Clinical Safety of Sandoz Denosumab Biosimilar vs Originator
December 11th 2024Sandoz's biosimilar denosumab (Jubbonti/Wyost) has demonstrated analytical, pharmacokinetic, pharmacodynamic, and clinical equivalence to reference denosumab (Prolia/Xgeva), supporting its approval and extrapolation to all approved indications.
A New Chapter: How 2023 Will Shape the US Biosimilar Space for 2024 and Beyond
December 31st 2023On this episode of Not So Different, Cencora's Brian Biehn and Corey Ford take a look back at major policy and regulatory advancements in 2023 and how these changes will alter the space going forward.
Pertuzumab Biosimilar Shows Promise in HER2-Positive Breast Cancer Treatment
December 9th 2024The proposed pertuzumab biosimilar QL1209 demonstrated equivalent efficacy and safety to reference pertuzumab (Perjeta) in neoadjuvant treatment of HER2-positive, ER/PR-negative early or locally advanced breast cancer, offering a cost-effective alternative with comparable clinical outcomes.
Switching to Rituximab Biosimilars Is Safe, Effective for Patients With Oncohematological Diseases
December 5th 2024Patients with oncohematological diseases switching to rituximab biosimilars experienced similar safety and efficacy, highlighting biosimilars' potential for cost-effective treatment across various medical conditions.