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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™ as the first and only endothelin receptor...

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Idorsia Pharmaceuticals Ltd: JERAYGO (aprocitentan) recommended for approval in Europe for the treatment of resistant hypertension

Idorsia Pharmaceuticals Ltd: JERAYGO (aprocitentan) recommended for approval in Europe for the treatment of resistant hypertension
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JERAYGO (Aprocitentan) Recommended For Approval In Europe For The Treatment Of Resistant Hypertension

(MENAFN - GlobeNewsWire - Nasdaq) Ad hoc announcement pursuant to Art. 53 LR Idorsia receives a positive opinion from the Committee for Medicinal Products for Human Use for JERAYGOTM ... ...

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AstraZeneca: Voydeya approved in the EU as a treatment for HPN

AstraZeneca announces that Voydeya has been approved in the European Union as an adjunct to ravulizumab or eculizumab for the treatment of adult patients with paroxysmal nocturnal hemoglobinuria ...

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AstraZeneca (AZN) Announces Voydeya Approval in EU as add-on to ravulizumab or eculizumab

AstraZeneca (AZN) Announces Voydeya Approval in EU as add-on to ravulizumab or eculizumab
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Form 20-F Achilles Therapeutics For: Dec 31

Form 20-F Achilles Therapeutics For: Dec 31
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FDA approves Basilea's intravenous antibiotic Zevtera for three indications

FDA approves Basilea's intravenous antibiotic Zevtera for three indications
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European Commission Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults -March 28, 2024 at 06:46 am EDT

Decision marks the first approval in Europe for an anti-PD-1/L1 therapy in resectable NSCLC based on positive overall survival results and represents the sixth approval for KEYTRUDA in lung cancer in...

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European Commission Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults

European Commission Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults
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Merck (MRK) Announces EU Approval of KEYTRUDA Plus Chemotherapy for NSCLC

Merck (MRK) Announces EU Approval of KEYTRUDA Plus Chemotherapy for NSCLC
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