Annual General
Meeting 2019
Our AGM 2019 took place
on Friday May 3, 2019.
Phase 3 investigation of
aprocitentan for resistant
hypertension management
Phase 3 investigation of
clazosentan for patients with
cerebral vasospasm
Phase 3 investigation of
daridorexant for patients with
insomnia
Phase 3 investigation of
lucerastat for patients with
Fabry disease
| Event | When |
| Full-Year 2019 Financial Results reporting* | February 6, 2020 |
| First Quarter 2020 Financial Results reporting* | April 23, 2020 |
| Annual General Meeting of Shareholders | May 13, 2020 |
| Half-Year 2020 Financial Results reporting* | July 23, 2020 |
*We will be in a silent period for 10 days ahead of the financial reporting.
| 10 Jan 2020 | |
| 05 Dec 2019 | |
| 19 Nov 2019 |
Idorsia published its half year financial results 2019 on Tuesday July 23, 2019.
Idorsia published its full year financial results 2018 on Thursday February 7, 2019.
Idorsia published its half year financial results 2018 on Tuesday July 24, 2018.
In June 2018, Idorsia announced that the first patient had been enrolled into PRECISION, a Phase 3 study to investigate the efficacy and safety of aprocitentan for resistant hypertension management in adults.
In June 2018, Idorsia announced that it is initiating a Phase 3 study, REACT, to investigate the efficacy and safety of clazosentan for the prevention of clinical deterioration due to vasospasm-related delayed cerebral ischemia in patients following an aneurysmal subarachnoid hemorrhage. The company also gave an update on the Japanese registration program and the establishment of Idorsia Pharmaceuticals Japan.
In June 2018, Idorsia announced that the first patients had been enrolled in a registration study to investigate the effect of daridorexant (recommended INN for ACT-541468), a dual orexin receptor antagonist, for the treatment of adult and elderly patients with insomnia. NB: The proposed INN "nemorexant" was unsuccessful and will no longer be used in association with ACT-541468.
In May 2018, Idorsia announced that the first patient had been enrolled in a registration study to investigate the effect of lucerastat, as an oral monotherapy, for the treatment of adult patients with genetically confirmed Fabry disease, irrespective of their genetic mutation type.
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