Nuvalent, Inc.

Nuvalent, Inc.

NUVL
Nuvalent, Inc.US flagNASDAQ Global Select
91.35
USD
-1.66
- -
6.72BMarket Cap
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
TTM
Revenue per Share
- -
- -
- -
- -
- -
- -
- -
- -
Basic EPS, GAAP
-0.73
-0.64
-2.13
-1.65
-2.17
-3.93
- -
-6.05
Free Cash Flow per Basic Share
-0.6
-0.65
-1.84
-1.31
-1.71
-2.79
- -
-4.2
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
-1.07
-1.39
-3.59
-3.22
-4.92
-8.24
- -
-14.53
Tangible Book Value per Share
-1.07
-1.37
13.08
9.32
12.03
16.11
- -
15.78
Basic Weighted Avg Shares
16
23
22
50
58
66
- -
74
Sales/Revenue/Turnover
- -
- -
- -
- -
- -
- -
- -
- -
Operating Margin (%)
- -
- -
- -
- -
- -
- -
- -
- -
Depreciation Expense
- -
- -
- -
- -
- -
- -
- -
- -
Net Income, GAAP
-12
-15
-46
-82
-126
-261
-425
-450
Effective Tax Rate (%)
- -
- -
- -
- -
- -
- -
- -
- -
Profit Margin (%)
- -
- -
- -
- -
- -
- -
- -
- -
Working Capital
-1
6
282
459
695
1,078
1,301
1,227
LT Debt
2
2
- -
- -
- -
- -
- -
- -
Total Equity
-17
-31
285
463
701
1,070
1,248
1,174
Return on Invested Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)
- -
- -
- -
- -
- -
- -
- -
- -

Capital Structure

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
ST Debt
- -
- -
- -
LT Borrowings
- -
- -
- -
LT Finance Leases
- -
- -
- -
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
72
78
79
Market Capitalization
6,200
7,311
7,627

Working Capital

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
Total Current Assets
957
1,392
1,308
Cash, Cash Equivalents & STI
943
1,372
1,287
Accounts Receivable, Net
- -
- -
- -
Inventories
- -
- -
- -
Total Current Liabilities
89
91
81
Payables & Accruals
77
74
73
ST Debt
- -
- -
- -
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
-165.37%
16.69%
Free Cash Flow
- -
83.56%
48.71%
Net Income, GAAP
- -
103.78%
63.13%
Sales/Revenue/Turnover
- -
- -
- -
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
-0.69
-0.88
-1.28
-1.05
-3.93
2025
-1.18
-1.39
-1.7
-1.58
- -
2026
-1.39
- -
- -
- -
- -

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Company Description

APIChat
CEO
James R. Porter
Full Time Employees
162
Sector
Healthcare
Industry
Biotechnology
Address
One Broadway Cambridge MA United States of America 02142
IPO Date
Jul 29, 2021
Business
Nuvalent, Inc. (Nasdaq: NUVL) is a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for clinically proven kinase targets in patients with cancer. Founded in 2017 and headquartered in Cambridge, Massachusetts, the company leverages expertise in chemistry and structure-based drug design to develop small-molecule inhibitors that overcome resistance, minimize adverse events, address brain metastases, and drive durable responses; its operations are primarily conducted in the United States, targeting oncology patients with non-small cell lung cancer (NSCLC) and other solid tumors. Nuvalent advances a robust pipeline featuring lead candidates zidesamtinib (NVL-520), a novel brain-penetrant ROS1-selective inhibitor in Phase 2 of the ARROS-1 trial for TKI-pretreated and naive advanced ROS1-positive NSCLC and other solid tumors; neladalkib (NVL-655), a brain-penetrant ALK-selective inhibitor in Phase 2 of the ALKOVE-1 trial for advanced ALK-positive NSCLC and other solid tumors, with the ALKAZAR Phase 3 trial initiated in July 2025 for TKI-naive ALK-positive NSCLC; and NVL-330, a brain-penetrant HER2-selective inhibitor in Phase 1 of the HEROEX-1 trial for HER2-altered NSCLC, alongside multiple discovery-stage programs. Recent milestones include the completion of a rolling New Drug Application (NDA) submission for zidesamtinib in TKI-pretreated advanced ROS1-positive NSCLC patients in Q3 2025, with FDA acceptance under the Real-Time Oncology Review pilot program and presentation of supporting pivotal data from the ARROS-1 trial at the IASLC 2025 World Conference on Lung Cancer; positive pivotal data readout for zidesamtinib in June 2025 aligning with FDA on NDA strategy; initiation of the ALKAZAR Phase 3 trial for neladalkib in July 2025; FDA Breakthrough Therapy Designation for neladalkib received earlier in 2025; appointment of Christy Oliger to the board in June 2025; and publication in Molecular Cancer Therapeutics reinforcing zidesamtinib's design rationale in April 2025, alongside ongoing enrollment and preclinical data presentations at major conferences including AACR and ASCO.

Company News

APIChat
  • Nuvalent Announces Key Program and Business Updates, Strengthening Foundation for Global Leadership in ROS1- and ALK-positive NSCLC

  • Nuvalent Highlights Upcoming Data Presentations for Neladalkib and Zidesamtinib at the 2026 American Society of Clinical Oncology Annual Meeting

  • Nuvalent Highlights Recent Pipeline Progress, Reiterates Key Anticipated Milestones, and Reports First Quarter 2026 Financial Results

  • Nuvalent: A Precision Oncology Platform With Two Near-Term Shots On Goal

  • Guardant Health Announces Multi-Year Strategic Collaboration with Nuvalent to Develop Companion Diagnostics and Support Potential Commercialization of Targeted Cancer Therapies Using the Guardant Infinity™ Platform

  • Evergreen Capital Management LLC Purchases New Position in Nuvalent, Inc. $NUVL

  • Nuvalent to Present Pivotal Data from ALKOVE-1 Trial of Neladalkib in TKI Pre-treated Advanced ALK-positive NSCLC at the 2026 American Society of Clinical Oncology Annual Meeting

  • New Clinical and Preclinical Data for Investigational Candidate Zidesamtinib Presented at AACR Annual Meeting 2026

  • Nuvalent Announces Submission of New Drug Application to FDA for Neladalkib in TKI Pre-treated Advanced ALK-positive NSCLC

  • Alexandra Balcom Sells 11,430 Shares of Nuvalent (NASDAQ:NUVL) Stock

  • Nuvalent to Present New Preclinical and Clinical Data for Zidesamtinib, an Investigational ROS1-Selective Inhibitor, at AACR Annual Meeting 2026

  • Nuvalent, Inc. (NASDAQ:NUVL) Given Average Rating of “Moderate Buy” by Analysts

  • This Investor Sold $104 Million of Nuvalent Stock Amid Cancer Drug Developer's Nearly 30% Rally

  • Nuvalent, Inc. $NUVL Shares Sold by ArrowMark Colorado Holdings LLC

  • Does Nuvalent (NUVL) Have the Potential to Rally 37.26% as Wall Street Analysts Expect?

  • Nuvalent Outlines Recent Pipeline Progress, Reiterates Key Anticipated Milestones, and Reports Fourth Quarter and Full Year 2025 Financial Results

  • Biotech Fund Dumps $84 Million of Nuvalent With Stock Up 29%

  • Nuvalent Details FDA Timelines for ROS1, ALK Drugs as $1.4B Cash Fuels Global Launch Plans

  • Nuvalent to Participate in the Guggenheim Emerging Outlook: Biotech Summit 2026

  • Nuvalent, Inc. (NASDAQ:NUVL) Given Consensus Recommendation of “Moderate Buy” by Brokerages