NKTX

Nkarta Inc
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$196.97M
P/E Ratio
—
EPS
$-1.59
Beta
0.97
52W High
$3.72
52W Low
$1.70
50-Day MA
$2.58
200-Day MA
$2.51
Dividend Yield
—
Profit Margin
0.00%
Forward P/E
—
PEG Ratio
—

About Nkarta Inc

Nkarta, Inc., a clinical-stage biopharmaceutical company, develops and markets cell therapies for the treatment of cancer. The company is headquartered in South San Francisco, California.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)385
Gross Profit (TTM)$-36.22M
EBITDA$-113.44M
Operating Margin0.00%
Return on Equity-38.80%
Return on Assets-19.60%
Revenue/Share (TTM)$0.00
Book Value$3.46
Price-to-Book0.80
Price-to-Sales (TTM)1000000.00
EV/Revenue1000000.0
EV/EBITDA0.95
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)0.00%
Shares Outstanding$71.63M
Float$60.52M
% Insiders4.88%
% Institutions82.80%

Historical Volatility

HV 10-Day
47.36%
HV 20-Day
68.06%
HV 30-Day
66.27%
HV 60-Day
74.32%
HV Rank
31.7%

Volatility is currently contracting

Analyst Ratings

Consensus ($10.83 target)
1
Strong Buy
6
Buy

Latest News

Nkarta Targets ACR 2026 Data Reveal as Outpatient CAR NK Trials Advance

Nkarta NASDAQ: NKTX said it expects to present initial clinical data from its autoimmune disease programs at the American College of Rheumatology's 2026 Convergence meeting in November, including presentations in myositis, scleroderma and program-wide safety.

MarketBeat9/27/2026Positive
Nkarta to Participate in September Investor Conferences

SOUTH SAN FRANCISCO, Calif., Sept. 10, 2026 (GLOBE NEWSWIRE) -- Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biopharmaceutical company developing engineered natural killer (NK) cell therapies to treat autoimmune diseases, today announced its participation in the following investor conferences: September 16, 2026 H.C.

GlobeNewsWire9/10/2026Neutral
Cyllene Therapeutics Expands Leadership Team to Support Corporate Growth and Clinical Product Development

Paris, France and New York, USA , July 23, 2026 (GLOBE NEWSWIRE) -- Paris, France and New York, USA, July 23, 2026 – Cyllene Therapeutics (“Cyllene Tx”), the global leader in non-replicating HSV-1 (nrHSV-1) vector technology in neurology, today announced the appointment of Alyssa Levin to its Board of Directors, where she will also serve as Chair of the Audit Committee. The company has also strengthened its leadership team with two key additions. Clara Cambon-Thiebaud joins as Vice President, Regulatory Affairs, based in New York, and Céline Breda as Vice President, Chemistry Manufacturing and Controls (CMC). This leadership team expansion comes as Cyllene Tx advances its lead candidate, EG110A, towards late-stage clinical development for neurogenic bladder-related incontinence.

GlobeNewsWire7/23/2026Neutral
Nkarta Reports First Quarter 2026 Financial Results and Corporate Highlights

Enrollment ongoing at 4 billion cell dose level (12 billion cells in 3-dose cycle) across all indications in Ntrust-1 and Ntrust-2 Regulatory agreement supports expansion into community-based settings with outpatient dosing to reduce patient burden Initial clinical data from Ntrust-1 and Ntrust-2 expected to be presented at a medical meeting in 2026 Cash balance of $266.7 million on March 31, 2026, including cash, cash equivalents and investments, expected to fund operations into 2029 SOUTH SAN FRANCISCO, Calif., May 12, 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 first quarter ended March 31, 2026.

GlobeNewsWire5/12/2026Neutral
Nkarta Announces FDA Agreement on Outpatient Dosing of NKX019 in Autoimmune Disease, Expanding Access to Community Rheumatology Centers

SOUTH SAN FRANCISCO, Calif., April 15, 2026 (GLOBE NEWSWIRE) -- Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biotechnology company developing engineered natural killer (NK) cell therapies to treat autoimmune diseases, today announced that it has reached agreement with the U.S. Food and Drug Administration (FDA) on key changes to the ongoing Ntrust-1 and Ntrust-2 clinical trials. The protocol amendments are designed to alleviate the need for overnight stays and reduce the overall burden on patients, enabling outpatient administration of NKX019 – an investigational CAR-NK cell therapy – by community research centers and community rheumatologists.

GlobeNewsWire4/15/2026Neutral

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Data last updated: 9/28/2026