IDORSIA N Profil

Ad hoc announcement pursuant to Art. 53 LR Viatris and Idorsia will collaborate on the global development and commercialization of two Phase 3 assets, selatogrel and cenerimod. Idorsia to receive an upfront payment of USD 350 million, potential development and regulatory milestone payments, additional sales milestone payments and tiered royalties on annual net sales. Viatris and Idorsia will both contribute to the development costs for both programs. Includes future optionality to expand...

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The application includes data from the Phase 3 registration study of patients with resistant hypertension, where aprocitentan demonstrated a sustained blood pressure reduction over 48 weeks and was well-tolerated Allschwil, Switzerland – Dec ember 2 0 , 2022 Idorsia Ltd (SIX: IDIA) today announced that it has submitted a New Drug Application (NDA) to the US Food and Drug Administration (FDA) seeking approval for aprocitentan, Idorsia’s investigational, novel dual endothelin receptor...

Daridorexant, taken every night for up to 12 months, was well-tolerated with no signs of tolerance (loss of effect) or physical dependence, and no evidence of withdrawal or rebound insomnia upon treatment discontinuation Exploratory efficacy endpoints show sustained improvements in nighttime sleep variables and daytime functioning Allschwil, Switzerland – December 1 2 , 2022 Idorsia Ltd (SIX: IDIA) today announced the publication of “ Long-term safety and tolerability of daridorexant in...

Ad - hoc -M itteilu ng gemäss Art. 53 K R Allschwil, S chweiz – 8. Februar 202 2 Idorsia Ltd (SIX: IDIA) veröffentlichte heute die Finanzergebnisse für 2021. Operative H ighlights QUVIVIQ™ (Daridorexant) 25 mg und 50 mg von der amerikanischen Food and Drug Administration (FDA) für die Behandlung der Schlaflosigkeit bei Erwachsenen zugelassen Zulassungsantrag für Daridorexant zur Behandlung der Schlaflosigkeit bei Erwachsenen wird von europäischer Arzneimittelagentur EMA, Swissmedic und...

Idorsia hat die Woche gleich mit einer sehr guten Nachricht begonnen. Der Biotechkonzern erhielt für sein Schlafmittel ......

Ad hoc announcement pursuant to Art. 53 LR Idorsia receives US FDA approval of QUVIVIQ (daridorexant) 25 and 50 mg for the treatment of adults with insomnia The approval of QUVIVIQ™ – 25 & 50 mg – is based on a robust Phase 3 clinical program that demonstrated significant improvement versus placebo on objective measures of sleep onset and sleep maintenance, as well as patient reported total sleep time Idorsia’s first approved medicine is a new treatment option for the approximately 25...