- Bone Health
- Immunology
- Hematology
- Respiratory
- Dermatology
- Diabetes
- Gastroenterology
- Neurology
- Oncology
- Ophthalmology
- Rare Disease
- Rheumatology
Samsung Bioepis Launches Adalimumab Biosimilar in Australia
Through a partnership with Merck, Samsung Bioepis adds to its portfolio of biosimilars available in Australia.
Samsung Bioepis, of Incheon, Republic of Korea, is reporting that its adalimumab biosimilar Hadlima has been launched in Australia. The agent references AbbVie’s Humira and is indicated for the treatment of rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, adult and pediatric Crohn disease, ulcerative colitis, hidradenitis suppurativa, and plaque psoriasis.
“With the launch in Australia, Samsung Bioepis’ adalimumab is now available in 3 markets: Europe, Canada, and Australia,” the company said in a statement. Via a partnership with Biogen, Hadlima was originally launched in 2018 in Europe under the brand name Imraldi. It was made available in Canada in 2021 via a partnership with Merck, which is also assisting with the Australia launch.
Hadlima marks the third anti–tumor necrosis factor biosimilar Samsung Bioepis has launched in Australia. The others are etanercept (Brenzys) and infliximab (Renflexis) biosimilars, in 2016 and 2017, respectively.
Hadlima will be available on the Australian Pharmaceutical Benefits Scheme (PBS) starting April 1, 2021. The PBS subsidizes medicines for residents of Australia.
Julie Reed: Why 2024 Is Important for Biosimilars
April 17th 2024Julie Reed, executive director of the Biosimilars Forum, showcases how the biosimilar industry is expected to develop throughout 2024, including major policy changes and hope for continued improvement in market share for adalimumab biosimilars.
Decoding the Patent Puzzle: Navigating the Legal Landscape of Biosimilars
March 17th 2024On this episode of Not So Different, Ha Kung Wong, JD, an intellectual patent attorney and partner at Venable LLP, details the confusing landscape that is the US patent system and how it can be improved to help companies overcome barriers to biosimilar competition.
Alvotech’s Stelara Biosimilar, Selarsdi, Receives FDA Approval
April 16th 2024Alvotech’s Selarsdi (ustekinumab-aekn), a biosimilar referencing Stelara (ustekinumab), gained FDA approval, making it the second ustekinumab biosimilar and second for the company to be given the green light for the American market.
Biosimilars Rheumatology Roundup for February 2024—Podcast Edition
March 3rd 2024On this episode of Not So Different, The Center for Biosimilars® revisited all the major rheumatology biosimilar news from February 2024, including the FDA approval of the 10th adalimumab biosimilar, the promise for an oral delivery system for ustekinumab, and the impact of adalimumab products on COVID-19 antibodies.
BioRationality: Removing the Misconceptions Surrounding Interchangeability
April 15th 2024Sarfaraz K. Niazi, PhD, outlines the current state of interchangeable biosimilars in the US and policy changes needed to clear up misconceptions surrounding the meaning behind interchangeability designations.
What Clinicians Need to Know About Using Biosimilars to Treat IBD
April 13th 2024A review article, intended to act as a guide for clinicians, summarizes the available infliximab and adalimumab biosimilars for treating inflammatory bowel disease (IBD) as well as others that are coming down the pipeline.
