Why Is Cancer-Focused Penny Stock Viracta Therapeutics Trading Higher On Wednesday?

Zinger Key Points
  • Viracta pauses the EBV+ solid tumor program to focus resources on more advanced EBV+ lymphoma program.
  • Viracta implements reduction in force that impacts approximately 23% of its employees.

Wednesday, Viracta Therapeutics Inc. VIRX stock is trading higher after the company reported Phase 2 NAVAL-1 trial results from Stages 1 and 2 of the relapsed or refractory (R/R) Epstein-Barr virus-positive (EBV+) peripheral T-cell lymphoma (PTCL) cohort.

Twenty-one patients with primarily Stage III-IV disease received nanatinostat in combination with valganciclovir.

  • As of the June 28 data cutoff, combined Stages 1 and 2 data demonstrated:
    • In the R/R EBV+ PTCL population: In the intent-to-treat (ITT) population (n=21), the overall response rate (ORR) was 33%, and the complete response rate (CRR) was 19%.
    • In the efficacy-evaluable (EE) population (n=17), the ORR was 41%, and the CRR was 24%.
    • In the second-line EBV+ PTCL subpopulation: The ORR was 60%, and the CRR was 30% in the ITT population (n=10).
    • The ORR was 67%, and the CRR was 33% in the EE population (n=9).
    • The median duration of response (DOR) has not yet been reached. Two responding patients proceeded to hematopoietic stem-cell transplant without relapse, one of whom remains in response over 16 months.
  • Nana-val was generally well-tolerated:

Additionally, the company received FDA feedback, which clarified the potential regulatory path to the initial registration of Nana-val in patients with R/R EBV+ PTCL.

Based on the FDA’s feedback, Viracta plans to begin a randomized controlled trial of Nana-val in the second half of 2025.

Viracta said it will focus Nana-val’s clinical development on patients with R/R EBV+ PTCL as follows:

  • First, the company will focus the primary analysis on the second-line EBV+ PTCL subpopulation in the ongoing NAVAL-1 trial’s expansion phase.
  • Second, the company plans to begin an RCT of Nana-val in 2025 for the second-line treatment of EBV+ PTCL patients.

Viracta believes this strategy will best position Nana-val for a potential NDA filing in 2026 for accelerated approval.

Viracta has aligned resources to prioritize its EBV+ lymphoma program.

Hence, the company has paused the EBV+ solid tumor program to focus resources on the more advanced EBV+ lymphoma program.

Along with this pipeline reprioritization, a force reduction has been implemented, which impacts approximately 23% of the company’s employees.

Price Action: VIRX stock is up 4.30% at $0.49 during the premarket session at last check Wednesday.

Photo via Shutterstock

Read Next:

Don’t miss the opportunity to dominate in a volatile market at the Benzinga SmallCAP Conference on Oct. 9-10 at the Chicago Marriott Downtown Magnificent Mile. Get exclusive access to CEO presentations, 1:1 meetings with investors, and valuable insights from top financial experts. Whether you’re a trader, entrepreneur, or investor, this event offers unparalleled opportunities to grow your portfolio and network with industry leaders. Secure your spot and get your tickets today!

Market News and Data brought to you by Benzinga APIs
Comments
Loading...
Posted In: EquitiesNewsMoversBriefsStories That Matterwhy it's moving
Benzinga simplifies the market for smarter investing

Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.

Join Now: Free!