STOCKHOLM, Nov. 14, 2019 /PRNewswire/ -- "This third quarter of 2019 saw us move steadily towards full recruitment of the NefIgArd study, despite a somewhat slower pace during the summer months. We can now see the finish line and we hope that the next couple of months develop as planned so that we can achieve our ambitious goal. Due to our interactions with the FDA during the year, we have been able to achieve acceptance by the FDA of a revised design of the confirmatory part of our study, using a more sensitive endpoint, which reduces the number of patients and shortens the confirmatory part of the trial substantially. We also received positive advice from EMA related to our revised study design as well as a confirmed path forward towards conditional approval in Europe."
Renée Aguiar-Lucander, CEO
Summary of Q3 2019
July 1 - September 30, 2019
Significant events during Q3 2019, in summary
Significant events after the end of reporting period, in summary
Investor presentation November 14, 15:00 CET
Audio cast with teleconference, Q3 2019, November 14, 2019, 15:00 (Europe/Stockholm)
Webcast: https://tv.streamfabriken.com/calliditas-therapeutics-q3-2019
Teleconference: Dial-in number SE +46850558368 UK: +443333009266 US: +18335268395
Financial calendar
Year-end report for the period January 1 - December 31, 2019 February 14, 2020
Interim report for the period January 1 - March 31, 2020 May 14, 2020
Interim report for the period January 1 - June 30, 2020 August 13, 2020
Interim report for the period January 1 - September 30, 2020 November 12, 2020
For further information, please contact:
Renée Aguiar-Lucander, CEO at Calliditas
Email: [email protected]
Telephone: +46 722 52 10 06
Mikael Widell, Head of Communications at Calliditas
Email: [email protected]
Telephone: +46 703 11 99 60
The information was submitted for publication, through the agency of the contact persons set out above, at 07:00 CET on November 14, 2019.
About Calliditas Therapeutics
Calliditas Therapeutics is a specialty pharmaceutical company based in Stockholm, Sweden. It is focused on developing high quality pharmaceutical products for patients with a significant unmet medical need in niche indications, in which the Company can partially or completely participate in the commercialization efforts. The Company is focused on the development and commercialization of the product candidate Nefecon, a unique formulation optimized to combine a time lag effect with a concentrated release of the active substance budesonide, within a designated target area. This patented, locally acting formulation is intended for treatment of patients with the inflammatory renal disease IgA nephropathy (IgAN). Calliditas Therapeutics is running a global Phase 3 study within IgAN and aims to commercialize Nefecon in the US. The company is listed on Nasdaq Stockholm (ticker: CALTX). Visit www.calliditas.com for further information.
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The following files are available for download:
Release | |
https://mb.cision.com/Public/16574/2961095/9346d030049768f5.pdf | press release Q3 2019 ENG |
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