ContraFect Announces First Patient Dosed in Pivotal Phase 3 DISRUPT Study of Exebacase as a Treatment for Staph aureus Bacteremia, Including Right-Sided Endocarditis
ContraFect Corporation (CFRX)
Last contrafect corporation earnings: 3/18 07:00 am
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Source: GlobeNewswire
YONKERS, N.Y., Jan. 10, 2020 (GLOBE NEWSWIRE) -- ContraFect Corporation (Nasdaq:CFRX), a clinical-stage biotechnology company focused on the discovery and development of direct lytic agents (DLAs), including lysins and amurin peptides, as new medical modalities for the treatment of life-threatening, antibiotic-resistant infections, today announced the first patient has been dosed in the Phase 3 DISRUPT (Direct Lysis of Staph aureus Resistant Pathogen Trial) study of exebacase in patients with Staph aureus bacteremia, including right-sided endocarditis. “We are pleased by the rapid enrollment and dosing of the first patient in the Phase 3 pivotal study of our lead lysin candidate, exebacase, which we believe has the potential to improve clinical outcomes for patients suffering and dying from Staph aureus bacteremia, particularly those infected with difficult to treat methicillin-resistant Staph aureus (MRSA). We are confident in the protocol for the Phase 3 study which aims to be
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