Viracta Therapeutics Reports First Quarter 2024 Financial Results and Provides Business Update
Viracta Therapeutics, Inc. (VIRX)
Company Research
Source: GlobeNewswire
Presented positive topline Nana-val results from Stage 1 of the pivotal Phase 2 NAVAL-1 trial in patients with relapsed or refractory (R/R) Epstein-Barr virus-positive (EBV+) peripheral T-cell lymphoma (PTCL) Initial results from the ongoing NAVAL-1 trial further validate Nana-val’s “Kick and Kill” mechanism of action; additional data are expected in the third quarter of 2024 Plan to engage with U.S. Food and Drug Administration (FDA) in mid-2024 to align on requirements for accelerated approval and support speed to market strategy Progressed the Phase 1b/2 study of Nana-val in patients with advanced EBV+ solid tumors; on track to determine the recommended Phase 2 dose (RP2D) in the second half of 2024 Positive engagement with the Japanese Pharmaceuticals and Medical Devices Agency (PMDA) enables patients in Japan to be enrolled directly into the NAVAL-1 trial without a preceding Japanese Phase 1 safety/pharmacokinetics study SAN DIEGO, May 09, 2024 (GLOBE NEWSWIRE) -- Viracta
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