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Nkarta Reports Fourth Quarter and Full Year 2025 Financial Results and Corporate Highlights

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Nkarta (Nasdaq: NKTX) reported fourth-quarter and full-year 2025 results and clinical progress on March 25, 2026. The company had $295.1 million of cash and investments as of December 31, 2025, which it says will fund operations into 2029. Dose escalation for NKX019 advanced to 4 billion cells per dose on days 0, 3 and 7 (12 billion cells per cycle). Initial clinical data from Ntrust-1 and Ntrust-2 are targeted for presentation at a medical conference in 2026. Full-year R&D was $90.4 million and net loss was $104.1 million (or $1.41 per share).

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Positive

  • Cash balance of $295.1 million projected to fund operations into 2029
  • Dose escalation advanced to 4 billion cells per dose (12 billion per cycle) for NKX019
  • Planned initial clinical data presentation from Ntrust-1 and Ntrust-2 at a 2026 medical conference
  • Full-year R&D investment of $90.4 million supporting clinical development

Negative

  • Full-year net loss of $104.1 million (or $1.41 per share)
  • Fourth-quarter net loss of $27.4 million indicates ongoing cash burn
  • General and administrative expenses of $31.6 million for 2025

News Market Reaction – NKTX

+0.47%
10 alerts
+0.47% Session close to close
+5.5% Peak in 22 hr 37 min
$163.01M Market Cap
0.3x Rel. Volume

In the Mar 26 session, NKTX gained 0.47%, reflecting a mild positive market reaction. Argus tracked a peak move of +5.5% during that session. Our momentum scanner triggered 10 alerts that day, indicating notable trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement combines 2025 financials with clinical progress for NKX019, highlighting a $295.1M...
Analysis

This announcement combines 2025 financials with clinical progress for NKX019, highlighting a $295.1M year‑end cash position and projected funding into 2029. Management is dosing at 4 billion cells per treatment day and preparing Ntrust-1 and Ntrust-2 data for a 2026 conference. Recent earnings history shows repeated emphasis on extending runway through cost controls and restructuring. Investors may watch upcoming clinical data quality, cash use relative to R&D, and any further strategic shifts.

Key Figures

Cash balance: $295.1M Cash runway: into 2029 R&D expenses: $90.4M +5 more
8 metrics
Cash balance $295.1M Cash, cash equivalents and investments as of Dec 31, 2025
Cash runway into 2029 Management expects current cash to fund operations into 2029
R&D expenses $90.4M Research and development spend for full year 2025
G&A expenses $31.6M General and administrative expenses for full year 2025
Net loss FY 2025 $104.1M Net loss for full year 2025
EPS FY 2025 $1.41 per share Net loss per basic and diluted share for full year 2025
Net loss Q4 2025 $27.4M Net loss for the fourth quarter of 2025
NKX019 dose level 4 billion cells Per dose on days 0, 3 and 7 in current regimen

Previous Earnings Reports

5 past events · Latest: Nov 10 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Nov 10 Q3 2025 earnings Positive +2.5% Q3 2025 results, NKX019 progress and strong cash runway into 2029.
Aug 12 Q2 2025 earnings Positive +12.8% Q2 2025 results with $334.0M cash and continued NKX019 trial plans.
May 14 Q1 2025 earnings Negative -8.0% Q1 2025 loss, restructuring with 34% workforce reduction to extend runway.
Mar 26 FY 2024 results Negative +43.8% FY 2024 loss and major restructuring despite strong $380.5M cash balance.
Nov 07 Q3 2024 earnings Negative -2.5% Q3 2024 net loss, pipeline reprioritization and focus on autoimmune uses.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings releases have often produced sizable moves, with most reactions aligning with the tone of cash runway and operational updates, but one notable divergence followed a major restructuring.

Recent Company History

Over the past five earnings cycles from Nov 2024 to Nov 2025, Nkarta consistently emphasized a multi‑year cash runway and advancing NKX019 in autoimmune diseases. Cash declined from $405.3M in Q3 2024 to $316.5M by Q3 2025, while guidance still pointed to funding into 2029. Restructuring actions, including a 34% workforce reduction, reshaped spending. Today’s report continues that theme with a $295.1M year‑end balance, ongoing dose escalation, and reiterated runway into 2029.

Key Terms

dose escalation, generalized myasthenia gravis, systemic lupus erythematosus, b-cell depletion, +1 more
5 terms
dose escalation medical
"Dose escalation for NKX019 advanced to 4 billion cells per dose..."
Dose escalation is the process of gradually increasing the amount of a treatment or substance over time. In finance, it can refer to slowly raising investments or commitments to manage risk and assess performance. For investors, understanding dose escalation helps gauge how companies or strategies adjust their approaches, which can impact future growth or stability.
generalized myasthenia gravis medical
"investigator-sponsored trials of NKX019 in generalized myasthenia gravis..."
A chronic neurological condition in which the immune system disrupts the chemical signals between nerves and muscles, causing muscle weakness that typically fluctuates and worsens with activity. Think of it as a faulty light switch or loose wiring that prevents muscles from responding reliably; severity and daily variability make treatment and long-term management important. For investors, the condition matters because it defines patient need, market size, and demand for approved therapies, clinical trial outcomes, and reimbursement decisions that drive company valuation.
systemic lupus erythematosus medical
"investigator-sponsored trials of NKX019 in ... systemic lupus erythematosus."
Systemic lupus erythematosus is a chronic autoimmune disease in which the body's immune system mistakenly attacks healthy tissue, causing inflammation that can affect skin, joints, kidneys, heart, lungs and other organs. It matters to investors because disease severity, prevalence, and gaps in effective treatments drive demand for new drugs and diagnostics—think of it as a large, persistent market need where a successful therapy can change patient outcomes and create significant commercial value.
b-cell depletion medical
"maximize the depth and durability of B-cell depletion and clinical response..."
B-cell depletion is a medical treatment strategy that lowers or removes B cells, a type of white blood cell that makes antibodies and helps coordinate immune responses. For investors, it matters because therapies that deplete B cells can be major products for autoimmune diseases, certain blood cancers, or organ transplant care, affecting sales potential, safety profiles, and regulatory risk; think of it like reducing a specific unit in an army to stop friendly fire but increasing vulnerability to other attacks.
restricted stock units financial
"tax withholding obligations arising from the vesting and settlement of Restricted Stock Units..."
Restricted stock units are a type of company reward where employees are promised shares of stock, but they only fully own these shares after meeting certain conditions, like staying with the company for a set time. They matter because they can become valuable assets and are often used to motivate employees to help the company succeed.

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  • Dose escalation for NKX019 advanced to 4 billion cells per dose on days 0, 3 and 7 for a total of 12 billion cells per cycle
  • Initial clinical data from Ntrust-1 and Ntrust-2 targeted for presentation at a medical conference in 2026
  • Cash balance of $295.1 million on December 31, 2025, including cash, cash equivalents and investments, is expected to fund operations into 2029

SOUTH SAN FRANCISCO, Calif., March 25, 2026 (GLOBE NEWSWIRE) -- Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biotechnology company developing engineered natural killer (NK) cell therapies to treat autoimmune diseases, today reported financial results for the fourth quarter and year ended December 31, 2025. 

“2025 was a year of strategic importance for Nkarta as we onboarded a clinical team with deep autoimmune experience, right-sized our workforce to be a responsible steward of investor capital, and continued to advance our CAR-NK cell therapy platform through dose escalation in the clinic,” said Paul J. Hastings, Chief Executive Officer of Nkarta. “Thoughtfully leveraging our safety data, we are now dosing patients at 4 billion cells in a three-dose cycle for a total of 12 billion cells as we look to maximize the depth and durability of B-cell depletion and clinical response, positioning us to unlock the full potential of NKX019 for people living with autoimmune disease.”

“We look forward to sharing a comprehensive clinical update from Ntrust-1 and Ntrust-2 later this year with the aim of presenting a meaningful data set at a medical conference. With cash projected to fund operations into 2029, we remain focused on disciplined clinical execution as we continue enrollment in our Ntrust-1 and Ntrust-2 clinical programs.”

NKX019 Clinical Program Progress and Upcoming Milestones

  • Enrollment continued across Ntrust-1 and Ntrust-2, our multi-center, open-label, dose-escalation clinical trials evaluating NKX019 in multiple autoimmune diseases.
  • Patients are now being dosed at 4 billion cells per dose as part of ongoing dose escalation.
  • Enrollment remains open in both investigator-sponsored trials of NKX019 in generalized myasthenia gravis and systemic lupus erythematosus.
  • Initial clinical data from Ntrust-1 and Ntrust-2 are planned for presentation at a medical conference later this year.

Fourth Quarter and Full Year 2025 Financial Highlights 

  • Nkarta had cash, cash equivalents, restricted cash, and investments in marketable securities of $295.1 million as of December 31, 2025.
  • Research and development (R&D) expenses were $90.4 million for the full year 2025 and $25.3 million for the fourth quarter of 2025. Non-cash stock-based compensation expense included in R&D expense was $3.2 million for the full year 2025 and $0.7 million for the fourth quarter of 2025.
  • General and administrative (G&A) expenses were $31.6 million for the full year 2025 and $5.7 million for the fourth quarter of 2025. Non-cash stock-based compensation expense included in G&A expense was $5.4 million for the full year 2025 and $1.2 million for the fourth quarter of 2025.
  • Net loss was $104.1 million, or $1.41 per basic and diluted share, for the full year 2025. This net loss includes non-cash charges of $14.4 million that consisted primarily of share-based compensation, right-of-use asset impairment and depreciation expenses. Net loss was $27.4 million, or $0.37 per basic and diluted share, for the fourth quarter of 2025. This net loss includes non-cash charges of $3.3 million that consisted primarily of share-based compensation and depreciation expenses.

Financial Guidance

  • Nkarta expects its current cash and cash equivalents to fund its current operating plan into 2029.

About the Ntrust℠ Clinical Trials in Autoimmune Disease
Ntrust-1 (NCT06557265) and Ntrust-2 (NCT06733935) are multi-center, open label, dose escalation clinical trials in patients with autoimmune disease receiving lymphodepletion followed by CD19-targeted CAR-NK cell therapy. Both trials will assess the safety of NKX019 in people living with autoimmune diseases as well as its potential to achieve durable remission via a “reset” of the immune system through the elimination of pathogenic B cells.

The Ntrust trials are enrolling up to 12 patients per dose level per disease indication across systemic sclerosis, idiopathic inflammatory myopathy, ANCA-associated vasculitis, lupus nephritis, and primary membranous nephropathy.

In both studies, patients now receive a three-dose cycle of NKX019 on Days 0, 3, and 7 following lymphodepletion with fludarabine and cyclophosphamide or cyclophosphamide alone, if they have significant cytopenia at baseline. Leveraging the engineering of NKX019, no patients in either trial will receive supplemental cytokines or antibody-based therapeutics. This approach is designed to evaluate the single-agent activity of NKX019 and facilitate a more rapid path to regulatory approval. Patients in Ntrust-1 may also receive additional cycles, if necessary, to restore response or enable a deeper response.
   
About NKX019
NKX019 is an allogeneic, cryopreserved, off-the-shelf immunotherapy candidate that uses natural killer (NK) cells derived from the peripheral blood of healthy adult donors. It is engineered with a humanized CD19-directed chimeric antigen receptor (CAR) for enhanced cell targeting and a proprietary, membrane-bound form of interleukin-15 (IL-15) for greater persistence and activity without exogenous cytokine support. CD19 is a biomarker for normal B cells as well as those implicated in autoimmune disease. Nkarta is evaluating NKX019 in multiple autoimmune conditions.

About Nkarta
Nkarta is a clinical-stage biotechnology company advancing the development of allogeneic, off-the-shelf natural killer (NK) cell therapies for autoimmune diseases. By combining its cell expansion and cryopreservation platform with proprietary cell engineering technologies, Nkarta is building a pipeline of future cell therapies engineered for deep therapeutic activity and intended for broad access in the outpatient treatment setting. For more information, please visit the company’s website at www.nkartatx.com.

Cautionary Note on Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Words such as "anticipates," "believes," "expects," "intends," “plans,” “potential,” "projects,” “would” and "future" or similar expressions are intended to identify forward-looking statements. Examples of these forward-looking statements include, but are not limited to, statements concerning Nkarta’s expectations regarding any or all of the following: Nkarta’s position, plans, strategies, and timelines for the continued and future clinical development and commercial potential of NKX019 (including the future availability and disclosure of clinical data and other updates from Nkarta’s clinical trials); the therapeutic potential and tolerability of NKX019 for the treatment of autoimmune diseases, including as a result of advancing Nkarta’s dose escalation; and Nkarta’s expected cash runway.

Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. These risks and uncertainties include, among others: Nkarta’s limited operating history and historical losses; Nkarta’s lack of any products approved for sale and its ability to achieve profitability; the risk that the results of preclinical studies and early-stage clinical trials may not be predictive of future results; Nkarta’s ability to raise additional funding to complete the development and any commercialization of its product candidates; Nkarta’s dependence on the clinical success of NKX019; that Nkarta may be delayed in initiating, enrolling patients in or completing its clinical trials; competition from third parties that are developing products for similar uses; Nkarta’sability to obtain, maintain and protect its intellectual property; Nkarta’s dependence on third parties in connection with manufacturing, clinical trials and pre-clinical studies; the complexity of the manufacturing process for CAR NK cell therapies; and the success of Nkarta’s recent (and any future) cost containment measures.

These and other risks and uncertainties are described more fully in Nkarta’s filings with the Securities and Exchange Commission (“SEC”), including the “Risk Factors” section of Nkarta’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, filed with the SEC on November 10, 2025, and Nkarta’s other documents subsequently filed with or furnished to the SEC. All forward-looking statements contained in this press release speak only as of the date on which they were made. Except to the extent required by law, Nkarta undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.


Nkarta, Inc.
Condensed Statements of Operations
(in thousands, except share and per share data)
(Unaudited)

  Three Months Ended
December 31,
  Year Ended
December 31,
 
  2025  2024  2025  2024 
Operating expenses            
Research and development $25,281  $23,127  $90,429  $96,744 
General and administrative  5,680   7,796   31,568   31,450 
Total operating expenses  30,961   30,923   121,997   128,194 
Loss from operations  (30,961)  (30,923)  (121,997)  (128,194)
Other income, net:            
Interest income  3,296   4,894   15,494   19,317 
Other income, net  257   94   2,419   87 
Total other income, net  3,553   4,988   17,913   19,404 
Net loss $(27,408) $(25,935) $(104,084) $(108,790)
             
Net loss per share, basic and diluted $(0.37) $(0.35) $(1.41) $(1.60)
Weighted average shares used to compute net loss per share, basic and diluted  74,044,370   73,595,401   73,991,197   67,865,323 

  


Nkarta, Inc.
Condensed Balance Sheets
(in thousands)
(Unaudited)
  December 31, 
  2025  2024 
Assets      
Cash, cash equivalents, restricted cash and investments $295,129  $380,489 
Property and equipment, net  66,721   74,658 
Operating lease right-of-use assets  34,429   36,014 
Other assets  7,930   10,042 
Total assets $404,209  $501,203 
Liabilities and stockholders' equity      
Accounts payable, accrued and other liabilities $15,464  $12,954 
Operating lease liabilities  76,420   80,273 
Total liabilities  91,884   93,227 
Stockholders’ equity  312,325   407,976 
Total liabilities and stockholders' equity $404,209  $501,203 


Nkarta Media/Investor Contact:
Nadir Mahmood
Nkarta, Inc.
nmahmood@nkartatx.com


FAQ

How much cash did Nkarta (NKTX) report at December 31, 2025 and how long will it fund operations?

Nkarta reported $295.1 million in cash, cash equivalents and investments as of December 31, 2025. According to the company, that balance is expected to fund its current operating plan into 2029, supporting ongoing clinical programs.

What is the NKX019 dosing update announced by Nkarta (NKTX) on March 25, 2026?

Nkarta advanced dose escalation to 4 billion cells per dose administered on days 0, 3 and 7, totaling 12 billion cells per cycle. According to the company, the change aims to deepen and extend B-cell depletion and clinical response.

When will Nkarta (NKTX) present initial clinical data from Ntrust-1 and Ntrust-2?

Initial clinical data from Ntrust-1 and Ntrust-2 are planned for presentation at a medical conference later in 2026. According to the company, the company expects to share a comprehensive clinical update and present a meaningful data set.

What were Nkarta's (NKTX) 2025 research and development and net loss figures?

Nkarta reported $90.4 million in research and development expense for full-year 2025 and a net loss of $104.1 million (or $1.41 per share). According to the company, non-cash charges totaled about $14.4 million in 2025.

Is Nkarta (NKTX) still enrolling patients in its NKX019 trials and which indications are included?

Enrollment remains open in the multi-center Ntrust-1 and Ntrust-2 dose-escalation trials. According to the company, investigator-sponsored trials continue in generalized myasthenia gravis and systemic lupus erythematosus.