Nuvalent, Inc. (NUVL)

US — Healthcare Sector
Peers:   DICE  ACLX  PCVX  VRDN  VTYX  CGEM  KNSA  REPL  ASND  UTHR  CERE  TVTX  GPCR 

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Key Metrics & Ratings

  • symbol NUVL
  • Rev/Share 0.0
  • Book/Share 14.1194
  • PB 5.2948
  • Debt/Equity 0.0
  • CurrentRatio 14.4808
  • ROIC -0.3135

 

  • MktCap 5368422524.0
  • FreeCF/Share -2.846
  • PFCF -26.3419
  • PE -17.7938
  • Debt/Assets 0.0
  • DivYield 0
  • ROE -0.3135

 

  • Rating C-
  • Score 1
  • Recommendation Strong Sell
  • P/E Score 1
  • DCF Score 3
  • P/B Score 1
  • D/E Score 1

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
Upgrade NUVL UBS Neutral Buy -- $100 March 14, 2025
Initiation NUVL H.C. Wainwright -- Buy -- $110 Dec. 30, 2024
Initiation NUVL Barclays -- Overweight -- $100 Aug. 29, 2024

News

Nuvalent Outlines Recent Pipeline and Business Progress, Reiterates Key Anticipated Milestones, and Reports First Quarter 2025 Financial Results
NUVL
Published: May 08, 2025 by: PRNewsWire
Sentiment: Neutral

Topline pivotal data expected for zidesamtinib in TKI pre-treated ROS1-positive NSCLC population in the first half of 2025 in support of anticipated first NDA submission by mid-year 2025 Initiation of ALKAZAR Phase 3 randomized, controlled trial of neladalkib for front-line ALK-positive NSCLC planned for first half of 2025 Pivotal data for neladalkib in TKI pre-treated ALK-positive NSCLC population anticipated by year-end 2025 Strengthened leadership team with key internal promotions CAMBRIDGE, Mass. , May 8, 2025 /PRNewswire/ -- Nuvalent, Inc. (Nasdaq: NUVL), a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for clinically proven kinase targets in cancer, today outlined …

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image for news Nuvalent Outlines Recent Pipeline and Business Progress, Reiterates Key Anticipated Milestones, and Reports First Quarter 2025 Financial Results
Nuvalent Announces Publication in Molecular Cancer Therapeutics Reinforcing Rational Molecular Design of Zidesamtinib as a Novel ROS1-Selective Inhibitor
NUVL
Published: April 29, 2025 by: PRNewsWire
Sentiment: Neutral

CAMBRIDGE, Mass. , April 29, 2025 /PRNewswire/ -- Nuvalent, Inc. (Nasdaq: NUVL), a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for clinically proven kinase targets in cancer, today announced the publication of a manuscript in Molecular Cancer Therapeutics, a journal of the American Association for Cancer Research, which supports the rational molecular design of zidesamtinib, its novel and selective ROS1 inhibitor.

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image for news Nuvalent Announces Publication in Molecular Cancer Therapeutics Reinforcing Rational Molecular Design of Zidesamtinib as a Novel ROS1-Selective Inhibitor
Nuvalent to Participate in Upcoming March Investor Conferences
NUVL
Published: February 28, 2025 by: PRNewsWire
Sentiment: Neutral

CAMBRIDGE, Mass. , Feb. 28, 2025 /PRNewswire/ -- Nuvalent, Inc. (Nasdaq: NUVL), a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for clinically proven kinase targets in cancer, today announced that James Porter, Ph.D.

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image for news Nuvalent to Participate in Upcoming March Investor Conferences

About Nuvalent, Inc. (NUVL)

  • IPO Date 2021-07-29
  • Website https://www.nuvalent.com
  • Industry Biotechnology
  • CEO Dr. James R. Porter Ph.D.
  • Employees 162

Nuvalent, Inc., a clinical stage biopharmaceutical company, develops therapies for patients with cancer. Its lead product candidates are NVL-520, a brain-penetrant ROS1-selective inhibitor to inhibit ROS1 fusions that express the normal ROS1 kinase domain without any drug-resistant mutations and remain active in the presence of mutations conferring resistance to approved and investigational ROS1 inhibitors, which is under Phase I development; and NVL-655, a brain-penetrant ALK-selective inhibitor, to address the clinical challenges of emergent treatment resistance, central nervous system-related adverse events, and brain metastases that might limit the use of first-, second-, and third-generation ALK inhibitors that is under Phase I/II clinical trial. The company was incorporated in 2017 and is headquartered in Cambridge, Massachusetts.