Guangzhou, China/Budapest, Hungary– # October 9,
2024 – Bio-Thera Solutions (688177:SH; “Bio-Thera”), a commercial-stage
biopharmaceutical company developing a pipeline of innovative therapies and
biosesimilars, and Gedeon Richter (“Richter”) announce today they have reached an
exclusive commercialization and license agreement for BAT2206, a biosesimilar
candidate to Stelara® (ustekinumab).
Under the agreement, Bio-Thera will maintain
responsibility for development, manufacturing, and supply of BAT2206 and
Bio-Thera has filed BAT2206 for regulatory approval with EMA on 1 July 2024. Richter will
have exclusive rights to commercialize the product in the European Union (EU), the
UK, Switzerland and selected other countries.
Bio-Thera will receive an upfront payment of
US$8.5 million, as well as further development and commercial milestones of up
to US$101.5 million, subject to the fulfillment of certain conditions.
“We are pleased to establish this partnership
with Gedeon Richter for BAT2206”, said Dr. Shengfeng Li, CEO of Bio-Thera. “BAT2206
is an important product to Bio-Thera and we believe that Richter is the right
partner for helping Bio-Thera bring BAT2206 to the most patients possible in
the EU and UK.”
“We are pleased to announce that Richter has made another important step towards building a robust biosesimilar portfolio across its core commercial region” – said Dr. Erik Bogsch, Head of the Biotechnology Business Unit of Richter. “Subsequent to the acquisitions made earlier this year and the recent news of our denosumab filing, the current deal with Bio-Thera reinforces Richter’s presence and biosesimilar portfolio in Europe.”
About BAT2206 (ustekinumab)
BAT2206 is a proposed biosesimilar to Jansen’s Stelara® which is a human monoclonal antibody that inhibits the bioactivity of human IL-12 and IL-23 by preventing shared p40 from binding to the IL-12Rβ1 receptor protein expressed on the surface of immune cells. IL-12 and IL-23 are involved in inflammatory and immune responses, such as natural killer cell activation and CD4+ T-cell differentiation and activation. IL-12 and IL-23 have been implicated as important contributors to the chronic inflammation that is a hallmark of Crohn's disease and ulcerative colitis, among many other autoimmune diseases. In the EU, Stelara® is currently approved for the treatment of 1) moderate to severe plaque psoriasis in adults and children above the age of 6 years whose condition has not improved with, or who cannot use, other systemic (whole-body) psoriasis treatments, 2) active psoriatic arthritis, alone or combined with methotrexate, in adults, when the condition has not improved enough with other treatments called disease-modifying anti-rheumatic drugs (DMARDs), 3) moderately to severely active Crohn’s disease in adults whose condition has not improved enough with other treatments for Crohn’s disease or who cannot receive such treatments, 4) moderately to severely active ulcerative colitis in adults whose condition has not improved enough with other treatments for ulcerative colitis or who cannot receive such treatments.
About Bio-Thera Solutions
Bio-Thera Solutions, Ltd., a leading innovative, global biopharmaceutical company in Guangzhou, China, is dedicated to researching and developing novel therapeutics for the treatment of cancer, autoimmune, cardiovascular, eye diseases, and other severe unmet medical needs, as well as biosesimilars for existing, branded biologics to treat a range of cancer and autoimmune diseases. As a leader in next generation antibody discovery and engineering, the company has advanced multiple candidates into late-stage development, including four approved products: QLETLI® and BETAGRIN®(Bevifibatide Citrate Injection) in China, and TOFIDENCE/ BAT1806 and Avzivi® / Pobevcy® in the US, EU and China. In addition, the company has more than 20 promising candidates in clinical trials, focusing on immuno-oncology in the post-PD-1 era and targeted therapies such as ADCs. For more information, please visit www.qdrongyue.com/en/ or follow us on Twitter (@bio_thera_sol) and WeChat (Bio-Thera).
About Gedeon Richter
Gedeon Richter Plc. (www.gedeonrichter.com),
headquartered in Budapest/Hungary, is a major pharmaceutical company in Central
Eastern Europe, with an expanding direct presence in Western Europe, China,
Latin America, and Australia. Having reached a market capitalization of EUR
4.3bn (USD 4.7bn) by the end of 2023, Richter's consolidated sales were
approximately EUR 2.1bn (USD 2.3bn) during the same year. The product portfolio
of Richter covers many important therapeutic areas, including Women's
Healthcare, Central Nervous System, and Cardiovascular areas. Having the
largest R&D unit in Central Eastern Europe, Richter's original research
activity focuses on CNS disorders. With its widely acknowledged steroid
chemistry expertise, Richter is a significant player in the Women's Healthcare
field worldwide. Richter is also active in developing, manufacturing and commercializing
biosesimilars for the treatment of osteoporosis, rheumatoid arthritis and other
auto-immune diseases.
Bio-Thera Cautionary Note Regarding
Forward-Looking Statements
This news release contains certain forward-looking statements relating to BAT2206,
or the product pipelines in general of Bio-Thera Solutions. Readers are
strongly cautioned that reliance on any forward-looking statements involves
known and unknown risks and uncertainties. The forward-looking statements
include, among others, those containing "could," "may,"
"should," "will," "would,"
"anticipate," "believe," "plan,"
"promising," "potentially," or similar expressions. They
reflect the company's current views with respect to future events that are
based on what the company believes are reasonable assumptions in view of
information currently available to Bio-Thera Solutions, and are not a guarantee
of future performance or developments. Actual results and events may differ
materially from information contained in the forward-looking statements as a
result of a number of factors, including, but not limited to, risks and
uncertainties inherent in pharmaceutical research and development, such as the
uncertainties of pre-clinical and clinical studies. Other risks and
uncertainties include challenges in obtaining regulatory approvals,
manufacturing, marketing, competition, intellectual property, product efficacy
or safety, changes in global healthcare situation, changes in the company's
financial conditions, and changes to applicable laws and regulations, etc.
Forward-looking statements contained herein are made only as of the date of
their initial publication. Unless required by laws or regulations, Bio-Thera
Solutions undertakes no obligation to publicly update any forward-looking
statement, whether as a result of new information, future events, changes in
the company's views or otherwise.
1. Stelara® is a registered trademark of Johnson & Johnson
2. QLETLI® is a registered trademark of Bio-Thera Solutions, Ltd.
3. TOFIDENCETM is a trademark of Biogen MA Inc.
4. Avzivi® is a registered trademark of Sandoz AG
5. POBEVCY® is a registered trademark of Bio-Thera Solutions, Ltd.
6. BETAGRIN® is a registered trademark of Bio-Thera Solutions, Ltd.