STOCKHOLM, March 14, 2022 /PRNewswire/ -- Calliditas
Therapeutics AB (Nasdaq: CALT, Nasdaq Stockholm: CALTX)
("Calliditas") today announced that the company has expanded its
licensing agreement with Everest Medicines II Limited (HKG: 1952)
("Everest") to extend the territory covered to include South Korea.
"We continue to have a fruitful and positive collaboration with
Everest and are delighted that we have come to an agreement also
around South Korea," said CEO
Renée Aguiar-Lucander.
The extension results in an upfront payment of USD 3 million to Calliditas as well as additional
payments and royalties related to future potential approvals and
commercialisation of Nefecon in South
Korea. Calliditas and Everest entered into a license
agreement in 2019 to develop and commercialize Nefecon in
Greater China and Singapore for the chronic autoimmune kidney
disease IgA Nephropathy (IgAN).
For further information, please contact:
Marie Galay, IR Manager,
Calliditas
Tel.: +44 79 55 12 98 45, email: marie.galay@calliditas.com
The information was sent for publication, through the agency
of the contact persons set out above, on March 14, 2022 at 07:00
a.m. CET.
About Calliditas
Calliditas Therapeutics is a biopharma company based in
Stockholm, Sweden focused on
identifying, developing and commercializing novel treatments in
orphan indications, with an initial focus on renal and hepatic
diseases with significant unmet medical needs. Calliditas' lead
product, TARPEYO, has been approved by the FDA as the first and
only treatment of IgA nephropathy (IgAN), indicated for reduction
of proteinuria in adults with primary IgAN at risk of rapid disease
progression, generally a UPCR of ≥1.5g/gram. Calliditas has also
filed a marketing authorization application (MAA) with the European
Medicines Agency (EMA) for this drug product. Additionally,
Calliditas has initiated a clinical trial in primary biliary
cholangitis, and also plans to initiate a trial in head and neck
cancer, with NOX inhibitor product candidate setanaxib. Calliditas
is listed on Nasdaq Stockholm (ticker: CALTX) and the Nasdaq Global
Select Market (ticker: CALT).
Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995, as amended, including, without limitation, statements
regarding Calliditas' strategy, commercialization efforts, business
plans, regulatory submissions, clinical development plans and
focus. The words "may," "will," "could," "would," "should,"
"expect," "plan," "anticipate," "intend," "believe," "estimate,"
"predict," "project," "potential," "continue," "target," and
similar expressions are intended to identify forward-looking
statements, although not all forward-looking statements contain
these identifying words. Any forward-looking statements in this
press release are based on management's current expectations and
beliefs and are subject to a number of risks, uncertainties, and
important factors that may cause actual events or results to differ
materially from those expressed or implied by any forward-looking
statements contained in this press release, including, without
limitation, any related to Calliditas' business, operations,
continued FDA approval for TARPEYO, market acceptance of TARPEYO,
clinical trials, supply chain, strategy, goals and anticipated
timelines, competition from other biopharmaceutical companies, and
other risks identified in the section entitled "Risk Factors" in
Calliditas' reports filed with the Securities and Exchange
Commission. Calliditas cautions you not to place undue reliance on
any forward-looking statements, which speak only as of the date
they are made. Calliditas disclaims any obligation to publicly
update or revise any such statements to reflect any change in
expectations or in events, conditions, or circumstances on which
any such statements may be based, or that may affect the likelihood
that actual results will differ from those set forth in the
forward-looking statements. Any forward-looking statements
contained in this press release represent Calliditas' views only as
of the date hereof and should not be relied upon as representing
its views as of any subsequent date.
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SOURCE Calliditas Therapeutics