- Daten der OASIS 3 Studie ergänzen positive Topline-Ergebnisse von OASIS 1 und 2 Studien und unterstützen Erkenntnisse zur Wirksamkeit, und bieten zudem Langzeitsicherheitsdaten für Elinzanetant
- Bayer wird auf Basis der Daten aus OASIS-Studien 1, 2 und 3 Marktzulassung für die Behandlung vasomotorischer Symptome bei Frauen in den Wechseljahren beantragen
- Elinzanetant ist neuartiger dualer Neurokinin-1,3 (NK-1,3) einmal täglich oral zu verabreichender Rezeptor-Antagonist in der späten klinischen Entwicklung, der zur nicht-hormonellen Behandlung von vasomotorischen Symptomen im Zusammenhang mit Wechseljahren untersucht wird
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