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Samsung Bioepis Co.,
Ltd. announced that Brenzys – a biosimilar referencing Enbrel
(etanercept), also known as SB4 – received regulatory approval in
Canada for the treatment of rheumatoid arthritis and ankylosing
spondylitis. Brenzys will be commercialized in Canada by Merck Canada
Inc.
“As evidenced in
other markets, we believe Brenzys will help drive down healthcare costs
and increase patient access to one of the most widely used autoimmune
treatment options in Canada,” said Christopher Hansung Ko, president
& CEO of Samsung Bioepis. “We remain committed to advancing one of
the industry's largest biosimilar pipelines, so that more patients
across Canada can access affordable, high-quality treatment.”
Prior to receiving
approval in Canada, Samsung Bioepis’ SB4 etanercept biosimilar received
regulatory approvals from Korea’s Ministry of Food and Drug Safety
(MFDS) as Brenzys in September 2015, the European Commission (EC) as
Benepali in January 2016 and Australia’s Therapeutic Goods
Administration (TGA) as Brenzys in July 2016.
Samsung Bioepis is
responsible for the development and manufacture of all immunology and
oncology biosimilar candidates in its pipeline, including Brenzys, as
well as global clinical trials and regulatory registration in all
markets worldwide for these biosimilar candidates. Following approval,
Samsung Bioepis biosimilar products are marketed and distributed by its
commercialization partners, Biogen and Merck, which is known as MSD
outside the United States and Canada.
The regulatory submission
for Brenzys was based on data from a randomized, double-blind 52-week
phase III study, involving 596 patients with moderate to severe
rheumatoid arthritis across 70 sites in 10 countries, who were treated
with either weekly dose of subcutaneous 50 mg SB4 or Enbrel with
background methotrexate. At week 52, SB4 showed ACR20 response rate of
80.8% in the SB4 arm versus 81.5% in the Enbrel arm, fully supporting
the 24-week study results of 78.1% and 80.3%, respectively.
Samsung Bioepis
continues to advance a broad pipeline of 13 biosimilar candidates,
which includes the following six first-wave candidates that cover the
therapeutic areas of immunology, oncology and diabetes: SB4 biosimilar
candidate referencing Enbrel (etanercept); SB2 biosimilar candidate
referencing Remicade (infliximab); SB5 biosimilar candidate referencing
Humira (adalimumab); SB9 (MK-1293) biosimilar candidate referencing
Lantus (insulin glargine); SB3 biosimilar candidate referencing
Herceptin (trastuzumab); SB8 biosimilar candidate referencing Avastin
(bevacizumab)
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