Nuvalent Inc Overview
Industry: Biotechnology
Sector: Healthcare
Nuvalent, Inc., a clinical stage biopharmaceutical company, engages in the development of 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; 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 clinical trial; and NVL-330, a brain-penetrant human epidermal growth factor receptor 2 (HER2)-selective inhibitor designed to treat tumors driven by HER2ex20, brain metastases, and avoiding treatment-limiting adverse events including due to off-target inhibition of wild-type EGFR, which is ongoing IND-enabling studies. The company was incorporated in 2017 and is headquartered in Cambridge, Massachusetts. Nuvalent, Inc., a clinical stage biopharmaceutical company, engages in the development of 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-resist Read MoreMavefund brings filings, fundamentals, valuation, price history and news for Nuvalent Inc into one research view. The sections below show what strengthens or weakens the research case.
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Reported Results
What the company reported, with filing details kept small.
Quarterly result summary
Net loss was -$109.3M. R&D expense was $83.6M.
What changed
- Review the SEC source filing for the full reported results and management commentary.
Guidance / outlook
The company expects to continue to progress the ALKAZAR trial throughout 2026. HER2 Program • Enrollment is ongoing in the HEROEX-1 Phase 1a/1b clinical trial evaluating the overall safety and tolerability of NVL-330 for pre-treated patients with HER2-altered NSCLC.
Source: SEC EDGAR company-filed earnings materials. Dates are shown only for verification; review the source filing before relying on extracted report details.
Other recent earnings materials
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Recent News
Company-relevant articles from sources that pass the Mave Signal relevance and reliability checks.
GSK Lands FDA Approval for Nuvalent-Acquired Jideytro for NSCLC
Headline from Yahoo Finance: GSK Lands FDA Approval for Nuvalent-Acquired Jideytro for NSCLC.
GSK secures first lung cancer approval, validating $10.6bn Nuvalent bet
Headline from Yahoo Finance: GSK secures first lung cancer approval, validating $10.6bn Nuvalent bet.
GSK completes $10.6 billion acquisition of Nuvalent
Headline from Investing.com: GSK completes $10.6 billion acquisition of Nuvalent.
Halper Sadeh LLC is Investigating Whether ATAI, CCRN, NUVL are Obtaining Fair Deals for their Shareholders
Headline from GlobeNewswire: Halper Sadeh LLC is Investigating Whether ATAI, CCRN, NUVL are Obtaining Fair Deals for their Shareholders.
Form 4 Nuvalent Inc For: 15 July By Investing.com
Headline from Investing.com Canada: Form 4 Nuvalent Inc For: 15 July By Investing.com.
Nuvalent Investor Alert: Kahn Swick & Foti, LLC Investigates Adequacy of Price and Process in Proposed Sale of Nuvalent, Inc. - NUVL
Headline from Business Wire: Nuvalent Investor Alert: Kahn Swick & Foti, LLC Investigates Adequacy of Price and Process in Proposed Sale of Nuvalent, Inc. - NUVL.
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Financial Statements
Company-reported SEC EDGAR facts organized into the three core statements.
Source: SEC EDGAR companyfacts. Values are standardized company filings for research support, not personalized financial advice.