Artiva Biotherapeutics, Inc./$ARTV
1D1W1MYTD1Y5YMAX
Capital at risk
About Artiva Biotherapeutics, Inc.
Artiva Biotherapeutics Inc is a biopharmaceutical company. The company is engaged in advancing a pipeline of off-the-shelf, allogeneic NK cell therapies for the treatment of hematologic malignancies or solid tumors. The pipeline program of the company includes Artiva-Funded Trials and Collaborator-Funded Trials. The company pipeline includes AlloNK: is an allogeneic, off-the-shelf, cryopreserved NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity (ADCC) effect of mAbs to drive B-cell. Others products includes: CAR-NK(AB201),CAR-NK(AB205).
- Ticker
- $ARTV
- Sector
- Health
- Primary listing
- NASDAQ
- Employees
- 115
- Headquarters
- San Diego, United States
- Website
- www.artivabio.com
ARTV Metrics
BasicAdvanced
$345M
-
-$3.21
2.18
-
Price and volume
Market cap
$345M
Beta
2.18
52-week high
$14.53
52-week low
$2.71
Average daily volume
411K
Financial strength
Current ratio
24.16
Quick ratio
24.061
Long term debt to equity
0.019
Total debt to equity
0.028
Profitability
EBITDA (TTM)
-93.462
Management effectiveness
Return on assets (TTM)
-22.34%
Return on equity (TTM)
-36.58%
Valuation
Price to book
0.99
Price to tangible book (TTM)
0.99
Price to free cash flow (TTM)
-2.595
Free cash flow yield (TTM)
-38.54%
Free cash flow per share (TTM)
-2.717
Growth
Earnings per share change (TTM)
-1.64%
Bulls say / Bears say
AlloNK received FDA Regenerative Medicine Advanced Therapy designation for refractory rheumatoid arthritis, and Artiva plans to initiate an approximately 150-patient randomized Phase 3 trial in the second half of 2026. (Artiva Biotherapeutics)
Artiva reported $349.4 million in cash, cash equivalents and investments as of June 30, 2026, which management expects to fund operations into 2029 and reduce near-term financing risk around the planned registrational program. (Artiva Biotherapeutics)
The program has shown encouraging activity beyond refractory RA: EULAR 2026 presentations covered 31 patients across rheumatoid arthritis, Sjögren disease and systemic sclerosis, while the company highlighted an outpatient-compatible safety profile and deep B-cell depletion. (Artiva Biotherapeutics)
AlloNK’s lead efficacy signal remains early-stage: the company reported a 71% ACR50 response in only five of seven refractory-RA patients with six months of follow-up, while the larger randomized Phase 3 trial has yet to generate confirmatory data. (SEC)
Artiva remains loss-making and its spending is increasing as development advances: second-quarter 2026 R&D expense rose to $21.9 million and net loss widened to $25.0 million from $21.3 million a year earlier. (SEC)
The May 2026 financing materially diluted existing shareholders, with Artiva issuing 23.9 million common shares plus pre-funded warrants for another 2.2 million shares; the company explicitly disclosed that the transaction resulted in dilution. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 10 Sept 2026.
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