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Save the date: Calliditas to host a Capital Markets Day in Stockholm, Sweden, on January 20, 2021

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Calliditas Therapeutics will host a Capital Markets Day in Stockholm, Sweden, on January 20, 2021, featuring presentations from the management team and key opinion leaders. The event will cover an overview of the company's clinical development, including the successful topline data from the Phase 3 study, regulatory updates on Nefecon, and US commercialization plans. The program will run from 1:00 p.m. to 5:00 p.m. CET and will be accessible via webcast.

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STOCKHOLM, Dec. 9, 2020 /PRNewswire/ -- Calliditas Therapeutics AB (publ) ("Calliditas") today announced that the company will host a Capital Markets Day in Stockholm, Sweden, on January 20, 2021 for investors, analysts and media.

Presentations will be made by members of Calliditas' management team as well as invited key opinion leaders. The program will include an overview of the company's clinical development program, with a review of the recent successful topline data readout from the Phase 3 clinical study NefIgArd; the lead candidate drug Nefecon's regulatory path towards potential market approval; an update on preparations for US commercialization; and updates on the pipeline. There will be moderated Q&A sessions following the presentations.

The program will run from 1:00 p.m. CET to 5:00 p.m. CET and will be accessible through a webcast via the company's website.

The Capital Markets Day will be held in English. The presentations will be available on the company's website after the event. Further details will follow shortly.

If you wish to register now, please send an email to finance@calliditas.com

For further information, please contact:

Marie Galay, IR Manager, Calliditas

Tel.: +44 79 55 98 12 45, email: marie.galay@calliditas.com

The information was sent for publication through the agency of the contact persons set out above, on December 9, 2020 at 1:00 p.m. CET.

About Calliditas

Calliditas Therapeutics is a specialty pharmaceutical 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 candidate, Nefecon, is a proprietary, novel oral formulation of budesonide, an established, highly potent local immunosuppressant, for the treatment of the autoimmune renal disease IgA nephropathy, or IgAN, for which there is a high unmet medical need and there are no approved treatments. Calliditas is running a global Phase 3 study within IgAN and, if approved, aims to commercialize Nefecon in the United States. Calliditas is listed on Nasdaq Stockholm (ticker: CALTX) and the Nasdaq Global Select Market (ticker: CALT). Visit www.calliditas.com for further information.

This information was brought to you by Cision http://news.cision.com

https://news.cision.com/calliditas-therapeutics/r/save-the-date--calliditas-to-host-a-capital-markets-day-in-stockholm--sweden--on-january-20--2021,c3251677

The following files are available for download:

https://mb.cision.com/Main/16574/3251677/1346197.pdf

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Cision View original content:http://www.prnewswire.com/news-releases/save-the-date-calliditas-to-host-a-capital-markets-day-in-stockholm-sweden-on-january-20-2021-301189349.html

SOURCE Calliditas Therapeutics

FAQ

What is the date of Calliditas' Capital Markets Day?

Calliditas' Capital Markets Day is scheduled for January 20, 2021.

Where will the Capital Markets Day be held?

The Capital Markets Day will be held in Stockholm, Sweden.

What will be discussed at the Capital Markets Day?

Topics will include the clinical development program, Phase 3 study data, Nefecon's regulatory path, and US commercialization plans.

What time does the Capital Markets Day start?

The event will start at 1:00 p.m. CET and end at 5:00 p.m. CET.

How can I access the Capital Markets Day presentations?

The presentations will be available via webcast on Calliditas' website.

What is Nefecon?

Nefecon is Calliditas' lead product candidate for treating IgA nephropathy, currently in Phase 3 clinical studies.

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