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Nkarta Reports Second Quarter 2026 Financial Results and Corporate Highlights

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Nkarta (Nasdaq: NKTX) reported second quarter 2026 results, highlighting continued enrollment in its Ntrust-1 and Ntrust-2 trials of NKX019 across multiple autoimmune diseases at a 4 billion cell dose per infusion, given as a three-dose 12 billion cell cycle in the outpatient setting.

Outpatient dosing is underway at community-based sites, with the option for additional NKX019 cycles if needed, and initial clinical data are planned for presentation at a medical conference in 2026. Nkarta reported $243.2 million in cash, cash equivalents, restricted cash and marketable securities at June 30, 2026, and expects this to fund its current operating plan into 2029. Second quarter 2026 R&D expense was $29.0 million, G&A expense was $14.1 million, and net loss was $40.4 million, or $0.54 per share, including $11.8 million of non-cash charges.

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Positive

  • Cash and investments $243.2M at June 30, 2026
  • Runway into 2029 based on current operating plan and cash position
  • NKX019 enrollment ongoing in Ntrust-1 and Ntrust-2 at 4B cells x 3 doses
  • Outpatient dosing initiated at community-based sites for broader patient access
  • Initial Ntrust data planned for presentation at a medical conference in 2026

Negative

  • Q2 2026 net loss $40.4M vs $23.0M in Q2 2025
  • R&D expenses $29.0M in Q2 2026 vs $20.8M in Q2 2025
  • G&A expenses $14.1M in Q2 2026 vs $6.4M in Q2 2025
  • Non-cash impairment $8.0M of right-of-use assets, leasehold improvements and equipment
  • Cash and investments declined to $243.2M from $295.1M at December 31, 2025

Market Context

The prior earnings event recorded a -6.71% 24-hour reaction, adding historical context to this quart...
Analysis

The prior earnings event recorded a -6.71% 24-hour reaction, adding historical context to this quarterly update. Recent insider activity was net selling, and the active S-3 shelf includes a $100,000,000 ATM program; financing remains a risk factor to watch.

Key Figures

Dose per administration: 4 billion cells Three-dose cycle: 12 billion cells Cash and investments: $243.2 million +5 more
8 metrics
Dose per administration 4 billion cells Ntrust-1 and Ntrust-2; three-dose cycle
Three-dose cycle 12 billion cells Ntrust-1 and Ntrust-2
Cash and investments $243.2 million As of June 30, 2026
R&D expenses $29.0 million Second quarter of 2026
G&A expenses $14.1 million Second quarter of 2026
Net loss $40.4 million Second quarter of 2026
Net loss per share $0.54 per share Basic and diluted; second quarter of 2026
Non-cash charges $11.8 million Included in second-quarter 2026 net loss

Previous Earnings Reports

5 past events · Latest: May 12 (Negative)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 12 1Q26 earnings Negative -6.7% Quarterly loss increased while the stock registered a negative 24-hour reaction.
Mar 25 FY25 earnings Positive +0.5% Cash runway and clinical progress accompanied a positive 24-hour reaction.
Nov 10 3Q25 earnings Positive +2.5% Enrollment progress and complete B-cell depletion accompanied a positive reaction.
Aug 12 2Q25 earnings Positive +12.8% Cash runway and clinical leadership updates accompanied a positive reaction.
May 14 1Q25 earnings Negative -8.0% Restructuring and quarterly loss accompanied a negative 24-hour reaction.

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

Pattern Detected

Earnings-specific history showed aligned positive and negative reactions, including a -6.71% move after the prior quarterly release.

Key Terms

dose-escalation, outpatient dosing, lymphodepletion, CAR-NK, +2 more
6 terms
dose-escalation medical
"our multi-center, open-label, dose-escalation clinical trials"
Dose-escalation is the part of an early-stage clinical trial where researchers gradually increase a drug’s dose in small groups of participants to find the safest and most effective amount. Think of it like turning up the volume slowly to find the sweet spot: investors watch these results closely because they reveal safety risks, potential effectiveness, and how quickly a drug can move to later trials or approval, all of which affect the development timeline and commercial prospects.
outpatient dosing medical
"Following our recent agreement with the FDA on outpatient dosing"
Outpatient dosing describes the administration of a drug or therapy to a patient who is not admitted to a hospital, typically given at a clinic, doctor's office, or at home. Investors care because outpatient use changes how a treatment is delivered, reimbursed, manufactured, and priced — similar to a product moving from a specialty store to a mass-market aisle, it can affect potential patient reach, recurring revenue, logistics, and payer acceptance.
lymphodepletion medical
"receiving lymphodepletion followed by CD19-targeted CAR-NK cell therapy"
Lymphodepletion is a short medical treatment that lowers a patient’s lymphocytes, the immune cells that can interfere with certain cell-based therapies, to create a more supportive environment for the new therapy to work. Think of it like clearing a crowded garden bed before planting seeds: by temporarily reducing competing cells, the engineered therapy can take hold more effectively. Investors watch lymphodepletion because it affects clinical trial results, safety profiles, treatment adoption, and overall commercial potential.
CAR-NK medical
"CD19-targeted CAR-NK cell therapy"
CAR‑NK are immune cells (natural killer cells) that have been genetically given a chimeric antigen receptor so they can home in on and destroy specific diseased cells, typically cancer. Think of it like equipping a guard with GPS coordinates for a target: it makes the cell better at finding and killing the enemy. Investors watch CAR‑NK programs because they offer potential for powerful, off‑the‑shelf therapies with different safety and manufacturing profiles than traditional drugs, which can drive company value but also carry clinical and regulatory risk.
allogeneic medical
"an allogeneic, cryopreserved, off-the-shelf immunotherapy candidate"
Allogeneic describes a process or material involving different individuals of the same species, such as cells, tissues, or organs donated from one person to another. It is important to investors because products or treatments based on allogeneic sources can enable scalable, off-the-shelf solutions, potentially reducing costs and increasing accessibility in healthcare and biotech industries.
chimeric antigen receptor medical
"a humanized CD19-directed chimeric antigen receptor"
A chimeric antigen receptor is an engineered protein added to a patient’s immune cells that gives them a new, specific ability to recognize and attack cells carrying a particular marker (antigen) — like equipping police with a facial‑recognition app to find a suspect. For investors, CARs are the core technology behind targeted cell therapies: their clinical success, manufacturing complexity, safety profile, and regulatory approval determine treatment market potential, development costs, and company value.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • Enrollment continues across all indications in Ntrust-1 and Ntrust-2 at the 4 billion cell dose level (12 billion cells in 3-dose cycle)
  • Initial clinical data from Ntrust-1 and Ntrust-2 expected to be presented at a medical conference in 2026
  • Cash balance of $243.2 million on June 30, 2026, including cash, cash equivalents and investments, expected to fund operations into 2029

SOUTH SAN FRANCISCO, Calif., Aug. 10, 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 second quarter ended June 30, 2026.

"Expanding access to NKX019 in the communities where autoimmune patients already receive care is central to how we’re advancing this program," said Paul J. Hastings, Chief Executive Officer of Nkarta. "This quarter, we continued to enroll patients across all indications in Ntrust-1 and Ntrust-2 at the 4 billion cell dose level. Following our recent agreement with the FDA on outpatient dosing, we have begun administrating NKX019 through our expanding network of community-based sites, with re-dosing available, if needed, to patients in both trials. We look forward to presenting our initial clinical dataset from Ntrust-1 and Ntrust-2 at a medical conference in 2026."

NKX019 Clinical Program Progress and Upcoming Milestones

  • Enrollment continues across Ntrust-1 and Ntrust-2, our multi-center, open-label, dose-escalation clinical trials evaluating NKX019 in multiple autoimmune diseases.
  • Outpatient dosing is underway within our network of community-based sites, broadening patient access beyond those who can travel to academic medical centers.
  • Patients are being dosed at 4 billion cells per dose x 3 doses (12 billion cells total) across all indications in Ntrust-1 and Ntrust-2.
  • Initial clinical data from Ntrust-1 and Ntrust-2 are planned for presentation at a medical conference in 2026.

Second Quarter 2026 Financial Highlights

  • Nkarta had cash, cash equivalents, restricted cash, and investments in marketable securities of $243.2 million as of June 30, 2026.
  • Research and development (R&D) expenses were $29.0 million for the second quarter of 2026. Non-cash stock-based compensation expense included in R&D expense was $0.7 million for the second quarter of 2026.
  • General and administrative (G&A) expenses were $14.1 million for the second quarter of 2026. Non-cash stock-based compensation expense included in G&A expense was $1.1 million for the second quarter of 2026.
  • Net loss was $40.4 million, or $0.54 per basic and diluted share, for the second quarter of 2026. This net loss includes non-cash charges of $11.8 million that consisted primarily of share-based compensation of $1.9 million, depreciation of $2.7 million, and impairment of right-of-use assets, leasehold improvements and other equipment of $8.0 million.

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, rheumatoid arthritis, lupus nephritis, and primary membranous nephropathy. Additional participants may be enrolled if needed to refine patient populations for further study.

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 both trials may also receive additional cycles, if needed, 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 people living with autoimmune diseases. By harnessing the power of the innate immune system to eliminate pathogenic B cells driving the autoimmune response, Nkarta is advancing novel cell therapies engineered for deep therapeutic impact. The on-demand availability and outpatient dosing of our CAR-NK cells enables a broad population of patients with different autoimmune conditions to conveniently access NK cell therapy in community health settings. 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, accessibility and tolerability of NKX019 for the treatment of autoimmune diseases, including as a result of advancing Nkarta’s dose escalation and expansion of outpatient dosing in community-based settings; 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’s ability 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 March 31, 2026, filed with the SEC on May 12, 2026, 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 June 30,  Six Months Ended June 30, 
  2026  2025  2026  2025 
Operating expenses            
Research and development $29,046  $20,778  $54,034  $44,950 
General and administrative  14,082   6,408   19,970   18,800 
Total operating expenses  43,128   27,186   74,004   63,750 
Loss from operations  (43,128)  (27,186)  (74,004)  (63,750)
Other income, net:            
Interest income  2,538   3,970   5,376   8,346 
Other income, net  222   239   428   444 
Total other income, net  2,760   4,209   5,804   8,790 
Net loss $(40,368) $(22,977) $(68,200) $(54,960)
             
Net loss per share, basic and diluted $(0.54) $(0.31) $(0.92) $(0.74)
Weighted average shares used to compute net loss per share, basic and diluted  74,494,855   73,977,625   74,377,069   73,947,220 
                 


Nkarta, Inc.
Condensed Balance Sheets
(in thousands)
(Unaudited)
       
  June 30,
2026
  December 31,
2025
 
Assets      
Cash, cash equivalents, restricted cash and investments $243,178  $295,129 
Property and equipment, net  56,768   66,721 
Operating lease right-of-use assets  30,942   34,429 
Other assets  6,757   7,930 
Total assets $337,645  $404,209 
Liabilities and stockholders' equity      
Accounts payable, accrued and other liabilities $16,368  $15,464 
Operating lease liabilities  73,539   76,420 
Total liabilities  89,907   91,884 
Stockholders’ equity  247,738   312,325 
Total liabilities and stockholders’ equity $337,645  $404,209 
         

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


FAQ

What were Nkarta (NASDAQ: NKTX) second quarter 2026 financial results?

Nkarta reported a Q2 2026 net loss of $40.4 million, or $0.54 per share. According to Nkarta, research and development expenses were $29.0 million, general and administrative expenses were $14.1 million, and total operating expenses reached $43.1 million for the quarter.

How much cash does Nkarta (NKTX) have, and how long will it fund operations?

Nkarta held $243.2 million in cash, cash equivalents, restricted cash and investments as of June 30, 2026. According to Nkarta, this cash balance is expected to fund its current operating plan into 2029, providing several years of runway for its clinical programs.

What is the design of Nkarta's Ntrust-1 and Ntrust-2 trials of NKX019 in autoimmune disease?

Ntrust-1 and Ntrust-2 are multi-center, open-label, dose-escalation trials of CD19-targeted CAR-NK therapy NKX019 in autoimmune diseases. According to Nkarta, patients receive lymphodepletion followed by three NKX019 doses on Days 0, 3 and 7, without supplemental cytokines or antibody-based therapeutics.

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 2026. According to Nkarta, these data are expected to be presented at a medical conference in 2026, providing the first clinical readout for NKX019 in autoimmune indications.

Which autoimmune indications are included in Nkarta's Ntrust trials of NKX019?

The Ntrust trials enroll patients with systemic sclerosis, idiopathic inflammatory myopathy, ANCA-associated vasculitis, rheumatoid arthritis, lupus nephritis and primary membranous nephropathy. According to Nkarta, up to 12 patients per dose level per indication may be enrolled, with additional participants possible.

How is NKX019 dosed in Nkarta's Ntrust-1 and Ntrust-2 trials?

Patients receive 4 billion NKX019 cells per dose, given three times for a total of 12 billion cells per cycle. According to Nkarta, dosing occurs on Days 0, 3 and 7 after lymphodepletion, with optional additional cycles if needed.

What outpatient dosing strategy is Nkarta using for NKX019 in autoimmune diseases?

Nkarta has begun outpatient dosing of NKX019 through a network of community-based sites. According to Nkarta, this approach expands access beyond academic centers and allows patients in Ntrust-1 and Ntrust-2 to receive re-dosing cycles if needed to restore or deepen response.