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Idorsia Ltd (IDIA.SW)

Swiss - Swiss Delayed price. Currency in CHF
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1.9530-0.0590 (-2.93%)
At close: 05:31PM CEST
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Previous close2.0120
Open2.0120
Bid0.0000 x 0
Ask2.0200 x 0
Day's range1.9000 - 2.0500
52-week range1.2940 - 9.7500
Volume497,043
Avg. volume1,177,969
Market cap349.433M
Beta (5Y monthly)0.82
PE ratio (TTM)N/A
EPS (TTM)-2.1100
Earnings date21 May 2024
Forward dividend & yieldN/A (N/A)
Ex-dividend date16 Jun 2017
1y target est1.74
  • Globe Newswire

    Bondholders approve amended terms of the 2024 convertible bonds

    Ad hoc announcement pursuant to Art. 53 LR Bondholders approve amended terms of the 2024 convertible bonds The proposed amendments to the terms of the 2024 convertible bond have been approved by the bondholders and will become binding and effective upon approval by the higher cantonal composition authority. Allschwil, Switzerland – May 6, 2024Idorsia Ltd. (SIX: IDIA) today announced the positive outcome of a bondholder meeting held at 17:30 CEST on May 6, 2024. The bondholder meeting for holders

  • GlobeNewswire

    Idorsia increases the consent fee in connection with the proposed restructuring of the 2024 convertible bond

    Ad hoc announcement pursuant to Art. 53 LR The proposed consent fee will be increased to 8’000’000 Idorsia shares. All other matters as proposed on April 23, 2024, remain unchanged.The bondholder meeting will take place on May 6, 2024, in order to vote on the proposals published on April 23, 2024. Allschwil, Switzerland – May 1, 2024Idorsia Ltd (SIX: IDIA) today announced that in relation to the bondholder meeting for holders of its outstanding convertible bonds maturing on July 17, 2024 (ISIN:

  • Globe Newswire

    JERAYGO (aprocitentan) recommended for approval in Europe for the treatment of resistant hypertension

    Ad hoc announcement pursuant to Art. 53 LR Idorsia receives a positive opinion from the Committee for Medicinal Products for Human Use for JERAYGO™ (aprocitentan) as the first and only endothelin receptor antagonist for the treatment of resistant hypertension in adult patients in combination with at least three antihypertensive medicinal products.A CHMP positive opinion is one of the final steps before marketing authorization can be granted by the European Commission – a final decision is expect