Read the latest press releases from Calliditas Therapeutics by clicking on a title below.

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FDA grants Calliditas Therapeutics Accelerated Approval of TARPEYO™ (budesonide) to Reduce Proteinuria in IgA Nephropathy

Interim Report Q3, 2021

Calliditas announces poster presentations at ASN Digital Kidney Week 2021

Calliditas Therapeutics’ nomination committee for the AGM 2022

Calliditas announces acquisition of remaining Genkyotex minority shares

Updated regulatory timeline for review of MAA in Europe.

PDUFA goal date extension for Nefecon NDA in the U.S.

Number of shares and votes in Calliditas Therapeutics

Interim Report Q2, 2021

Calliditas Therapeutics has resolved on a directed share issue in the amount of 2.4 million shares, raising proceeds of approximately SEK 324 million

Calliditas Therapeutics intends to carry out a directed share issue

Calliditas Receives FDA Fast Track Designation for setanaxib in PBC

Calliditas Therapeutics and STADA partner to register and commercialize specialty therapy for IgA Nephropathy in Europe

Calliditas secures $75 million term loan facility

Calliditas Announces Submission of Marketing Authorisation Application for Nefecon to the European Medicines Agency

Calliditas Therapeutics to Present at Jefferies Virtual Healthcare Conference

Bulletin from the annual general meeting of Calliditas Therapeutics AB (publ)

Interim Report Q1, 2021

Calliditas Therapeutics to host conference call to provide Business Update for the first quarter of 2021

Calliditas promotes Andrew Udell to President, North America

FDA grants priority review for Nefecon, for patients with IgA nephropathy

Calliditas Therapeutics’ 2020 Annual Report Published

Change in financial calendar

Notice of annual general meeting of Calliditas Therapeutics AB (publ)

EMA Grants Accelerated Assessment Procedure for Nefecon for the Treatment of IgA Nephropathy

Calliditas Announces Submission of New Drug Application to U.S. FDA for Nefecon in Patients with Primary IgA Nephropathy

Calliditas strengthens its US Commercial and Medical Affairs Organization

Calliditas Therapeutics to Host Key Opinion Leader Perspectives Webinar on the Pathophysiology and Treatment of IgA Nephropathy in Clinical Practice

Year-End Report, 2020

First Patient Dosed in NefIgArd Open Label Extension Study

Calliditas announces termination of the proposed global offering

Calliditas Therapeutics launches proposed global offering

Calliditas Announces Full Enrollment of the Phase 3 NefIgArd Trial

Calliditas announces clinical development plan for setanaxib and comments on data from Part A of NefIgArd study at today´s R&D Day

Positive Phase 1 results in high-dose setanaxib trial

Agenda for Calliditas virtual R&D Day on January 20, 2021