Arvinas reported positive efficacy signals in both clinical-stage programs and closed an underwritten public offering of common stock, receiving net proceeds of $431.9 million. The company's cash, cash equivalents, and marketable securities are expected to fund operations into 2024.
Presented interim Phase 1 data for ARV-471 showing potential for best-in-class safety and tolerability and a robust efficacy signal in heavily pretreated patients with ER+/HER2- breast cancer.
Presented data from the ongoing dose escalation portion of the Phase 1/2 trial of ARV-110 in men with mCRPC, providing additional evidence of anti-tumor activity and patient benefit.
Closed an underwritten public offering of 6,571,428 shares of common stock at a public offering price of $70.00 per share, receiving net proceeds of $431.9 million.
Initiated the ARDENT Phase 2 dose expansion study of ARV-110 and the VERITAC Phase 2 dose expansion study of ARV-471.
Arvinas expects its cash, cash equivalents, and marketable securities will be sufficient to fund its planned operating expenses and capital expenditures into 2024.
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