STOCKHOLM, Dec. 21,
2022 /PRNewswire/ -- Calliditas Therapeutics AB
(publ) (Nasdaq: CALT, Nasdaq Stockholm: CALTX) ("Calliditas")
announced today that CEO Renée Aguiar-Lucander has net purchased
50,000 shares through Calliditas' warrant program 2019/2022.
Following the new subscription for shares, her shareholding in the
company will amount to 643,000 common shares.
The majority of the members of management who are eligible
option holders in the program have today net purchased shares via
the warrant program 2019/2022, which includes 422,500 warrants and
can be exercised up to and including December 31, 2022. To partially finance the share
purchases, the option holders in the program, including the CEO and
eligible members of management, have sold shares. This sale, which
consisted of 352,500 shares, was made today in a block
transaction.
" I am excited about the company's development and success to
date, including the promising start to our commercialization of
TARPEYO in the US and the significant progress of the franchise
such as regulatory filing in China, commercial launch in Europe and the addition of a partner in
Japan. I look forward to
continuing building value in our lead program backed by our
exciting late-stage pipeline, which also has the potential of
significant value creation in 2023," said Renée Aguiar-Lucander,
CEO of Calliditas Therapeutics.
All shares in the warrant program 2019/2022 have been subscribed
for, and Calliditas will receive SEK 31.5
million in cash.
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 Calliditas contact person set out above, on December 20, 2022 at 9:15
p.m. CET.
About Calliditas
Calliditas Therapeutics is a commercial stage 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, Nefecon, has been granted accelerated approval by the FDA
under the trade name TARPEYO® and conditional marketing
authorization by the European Commission under the trade name
Kinpeygo®. Kinpeygo is being commercialized in the European Union
Member States by Calliditas' partner, STADA Arzneimittel AG.
Additionally, Calliditas is conducting a Phase 2b/3 clinical trial in primary biliary
cholangitis and a Phase 2 proof-of-concept trial in head and neck
cancer with its NOX inhibitor product candidate, setanaxib.
Calliditas' common shares are listed on Nasdaq Stockholm (ticker:
CALTX) and its American Depositary Shares are listed on the Nasdaq
Global Select Market (ticker: CALT). Visit www.calliditas.com for
further information.
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, ,
market acceptance of Kinpeygo/TARPEYO, safety or efficacy of
Kinpeygo/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.
The following files are available for download:
https://mb.cision.com/Main/16574/3688063/1750220.pdf
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Warrant program
2019
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SOURCE Calliditas Therapeutics