|Full-Year 2018 Financial Results reporting*||February 7, 2019|
|First Quarter 2019 Financial Results reporting*||April 18, 2019|
|Annual General Meeting 2019||May 3, 2019|
|Half-Year 2019 Financial Results reporting*||July 23, 2019|
*We will be in a silent period for 10 days ahead of the financial reporting.
Phase 3 initiation: Aprocitentan for resistant hypertension management
Phase 3 Advancing: Clazosentan for cerebral vasospasm
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.
Phase 3 initiation: Nemorexant for insomnia
In June 2018, Idorsia announced that the first patients had been enrolled in a registration study to investigate the effect of nemorexant (proposed INN for ACT-541468), a dual orexin receptor antagonist, for the treatment of adult and elderly patients with insomnia.
Phase 3 initiation: Lucerastat for Fabry disease
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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