Viracta Therapeutics, Inc. (VIRX) — 0.84 (+0.036)

US NASDAQ — Healthcare Sector
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Key Metrics & Ratings

  • symbol VIRX
  • Rev/Share 0.0
  • Book/Share 0.7757
  • PB 0.6348
  • Debt/Equity 0.8518
  • CurrentRatio 1.769
  • ROIC -0.8839

 

  • MktCap 19018753.0
  • FreeCF/Share -0.975
  • PFCF -0.5043
  • PE -0.3927
  • Debt/Assets 0.3847
  • DivYield 0
  • ROE -1.0602

 

  • Rating B+
  • Score 3.0
  • Recommendation Neutral
  • P/E Score 2.0
  • DCF Score 5.0
  • P/B Score 4.0
  • D/E Score 4.0

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
No ratings available.

News

Viracta Therapeutics Appoints Michael Faerm as Chief Financial Officer
VIRX
Published: May 14, 2024 by: GlobeNewsWire
Sentiment: Neutral

SAN DIEGO, May 14, 2024 (GLOBE NEWSWIRE) -- Viracta Therapeutics, Inc. (Nasdaq: VIRX), a clinical-stage precision oncology company focused on the treatment and prevention of virus-associated cancers that impact patients worldwide, today announced the appointment of Michael Faerm as Chief Financial Officer, effective immediately. Mr. Faerm is a seasoned biotech executive with more than 25 years of experience in life sciences companies, equity research and investment banking.

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image for news Viracta Therapeutics Appoints Michael Faerm as Chief Financial Officer
Viracta Therapeutics Announces Positive Topline Nana-val Results from Stage 1 of the NAVAL-1 Trial in Patients with Relapsed or Refractory Epstein-Barr Virus-Positive (EBV+) Peripheral T-Cell Lymphoma
VIRX
Published: April 15, 2024 by: GlobeNewsWire
Sentiment: Neutral

- Patients in the Nana-val (nanatinostat in combination with valganciclovir) treatment arm achieved clinically meaningful anti-tumor responses with an overall response rate of 50% and a complete response rate of 20% in the intent-to-treat population (71% and 29% in the efficacy-evaluable population) with a generally manageable safety profile -

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image for news Viracta Therapeutics Announces Positive Topline Nana-val Results from Stage 1 of the NAVAL-1 Trial in Patients with Relapsed or Refractory Epstein-Barr Virus-Positive (EBV+) Peripheral T-Cell Lymphoma
Viracta Therapeutics to Present Topline Nana-val Results from Stage 1 of the NAVAL-1 Trial at the 2024 Annual Congress of The Hematology Society of Taiwan
VIRX
Published: April 01, 2024 by: GlobeNewsWire
Sentiment: Neutral

The oral presentation will focus on topline Stage 1 data from both arms of the relapsed or refractory EBV+ peripheral T-cell lymphoma cohort (in patients randomized to either nanatinostat monotherapy [n=10] or to nanatinostat in combination with valganciclovir [Nana-val, n=10]), with an aim to clearly delineate the differentiation of Nana-val's ‘Kick and Kill' mechanism of action The oral presentation will focus on topline Stage 1 data from both arms of the relapsed or refractory EBV+ peripheral T-cell lymphoma cohort (in patients randomized to either nanatinostat monotherapy [n=10] or to nanatinostat in combination with valganciclovir [Nana-val, n=10]), with an aim to …

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image for news Viracta Therapeutics to Present Topline Nana-val Results from Stage 1 of the NAVAL-1 Trial at the 2024 Annual Congress of The Hematology Society of Taiwan
Viracta Therapeutics to Present at the Oppenheimer 34th Annual Healthcare Life Sciences Conference
VIRX
Published: February 06, 2024 by: GlobeNewsWire
Sentiment: Neutral

SAN DIEGO, Feb. 06, 2024 (GLOBE NEWSWIRE) -- Viracta Therapeutics, Inc. (Nasdaq: VIRX), a clinical-stage precision oncology company focused on the treatment and prevention of virus-associated cancers that impact patients worldwide, today announced that Mark Rothera, its President and Chief Executive Officer, and Darrel P. Cohen, M.D., Ph.D., its Chief Medical Officer, are scheduled to participate in a virtual fireside chat at the Oppenheimer 34th Annual Healthcare Life Sciences Conference on Tuesday, February 13, 2024, at 9:00 a.m. PT/12:00 p.m. ET.

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image for news Viracta Therapeutics to Present at the Oppenheimer 34th Annual Healthcare Life Sciences Conference
Viracta Therapeutics Provides Clinical Update and Outlook for 2024
VIRX
Published: January 04, 2024 by: GlobeNewsWire
Sentiment: Neutral

Speed to market strategy for Nana-val in patients with relapsed or refractory EBV + peripheral T-cell lymphoma supported by complete enrollment of Stage 1, complete enrollment of Stage 2 anticipated in Q1 2024 and engagement with the FDA on potential accelerated approval pathway by mid-2024

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image for news Viracta Therapeutics Provides Clinical Update and Outlook for 2024
Viracta Therapeutics Announces Orphan Drug Designation Granted by the U.S. FDA to Nana-val for the Treatment of Nasopharyngeal Carcinoma
VIRX
Published: December 12, 2023 by: GlobeNewsWire
Sentiment: Neutral

First orphan drug designation for Nana-val granted in EBV + solid tumors Seventh orphan drug designation for Nana-val globally; fifth granted by the FDA SAN DIEGO, Dec. 12, 2023 (GLOBE NEWSWIRE) -- Viracta Therapeutics, Inc. (Nasdaq: VIRX), a clinical-stage precision oncology company focused on the treatment and prevention of virus-associated cancers that impact patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has granted an orphan drug designation (ODD) to Nana-val (nanatinostat in combination with valganciclovir), the company's all-oral investigational therapy targeting Epstein-Barr virus (EBV)-associated cancers, for the treatment of nasopharyngeal carcinoma (NPC). This represents the first …

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image for news Viracta Therapeutics Announces Orphan Drug Designation Granted by the U.S. FDA to Nana-val for the Treatment of Nasopharyngeal Carcinoma
Viracta Therapeutics Announces Interim Data from Phase 1b/2 Clinical Trial of Nana-val in Patients with Epstein-Barr Virus-Positive Solid Tumors that Show Confirmed Tumor Responses at Higher Dose Levels
VIRX
Published: December 04, 2023 by: GlobeNewsWire
Sentiment: Neutral

Confirmed partial responses without dose-limiting toxicities during dose escalation along with new preclinical data support the opportunity to further enhance efficacy through a novel split daily dosing regimen at higher dose levels of Nana-val

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image for news Viracta Therapeutics Announces Interim Data from Phase 1b/2 Clinical Trial of Nana-val in Patients with Epstein-Barr Virus-Positive Solid Tumors that Show Confirmed Tumor Responses at Higher Dose Levels
Viracta Therapeutics Reports Third Quarter 2023 Financial Results and Provides Business Update
VIRX
Published: November 09, 2023 by: GlobeNewsWire
Sentiment: Neutral

Reported preliminary clinical data from the pivotal NAVAL-1 clinical trial of Nana-val in patients with relapsed or refractory EBV + peripheral T-cell lymphoma showing an overall response rate and complete response rate of 40%

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image for news Viracta Therapeutics Reports Third Quarter 2023 Financial Results and Provides Business Update
Viracta Therapeutics to Present at Upcoming Investor Conferences
VIRX
Published: November 07, 2023 by: GlobeNewsWire
Sentiment: Neutral

SAN DIEGO, Nov. 07, 2023 (GLOBE NEWSWIRE) -- Viracta Therapeutics, Inc. (Nasdaq: VIRX), a clinical-stage precision oncology company focused on the treatment and prevention of virus-associated cancers that impact patients worldwide, today announced that Company's Management will participate in upcoming investor conferences in November.

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image for news Viracta Therapeutics to Present at Upcoming Investor Conferences

About Viracta Therapeutics, Inc. (VIRX)

  • IPO Date 2005-09-27
  • Website https://www.viracta.com
  • Industry Biotechnology
  • CEO Mr. Mark Andrew Rothera
  • Employees 40

Viracta Therapeutics, Inc., a precision oncology company, engages in developing drugs for the treatment of virus-associated malignancies. Its lead product candidature includes Nana-val, in combination with nanatinostat and valganciclovir that is in Phase II clinical trial for Epstein-Barr virus-positive lymphoma; and open-label Phase 2 basket trial for the treatment of various relapsed/refractory Epstein-Barr virus-positive (EBV+) lymphoma, as well as an open-label Phase 1b/2 trial for the treatment of EBV+ recurrent or metastatic nasopharyngeal carcinoma and other EBV+ solid tumors. The company's development pipeline includes vecabrutinib, a clinical-stage non-covalent ITK/BTK inhibitor and VRx-510 (formerly SNS-510), a preclinical-stage PDK-1 inhibitor. It is evaluating development and collaboration opportunities for vecabrutinib in combination with chimeric antigen receptor T-cell therapies and VRx-510 in various oncology indications. The company was formerly known as Sunesis Pharmaceuticals, Inc. to Viracta Therapeutics, Inc. in February 25, 2021. Viracta Therapeutics, Inc. was incorporated in 1998 and is headquartered in Cardiff-by-the-Sea, California.