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Intellia Therapeutics, Inc.

NTLA· NASDAQ
$12.14-0.98%
2026-09-18

Financials

Valuation Metrics

Intellia Therapeutics, Inc.'s Market Cap is $1.70B. At end of 2025 it was $974M. Ranked #2138 of 3,121 in US market (top 69%), #838 of 1,463 on NASDAQ (top 57%), #153 of 266 in Pharmaceuticals, Biotechnology & Life Sciences (top 58%) by Market Cap.

Investment Metrics(as of 2026-09-18)

MetricValue
Size
Market Cap$1.70B
Revenue$60M
Net Income$-400M
Total Assets$857M
Net Assets$728M
Employees377
Value
P/B2.33x
P/S28.51x
FCF Yield-27.48%
Profitability
ROE-54.96%
ROA-46.66%
Op. Margin-711.66%
Revenue Growth12.58%
Financial Health
Debt Ratio17.79%
Total Debt$73M
FCF$-466M
Cash$106M
Current Ratio6.65x
Performance
1Y Return-24.64%
1M Return-8.58%
From 52W High-57.03%
1Y MDD-71.27%
Trading
Volume7,682,650 shares
Trading Value$93M
Per Share
EPS$-2.86
BPS$5.21

Company Info

CEO John Leonard
Employees 377
HQ Cambridge, US

Intellia Therapeutics, Inc. is a biotechnology firm dedicated to advancing therapeutic treatments through its expertise in genome editing. The company's pipeline includes several in vivo (administered within the body) programs. NTLA-2001 is currently undergoing a Phase 1 clinical trial for transthyretin amyloidosis, while NTLA-2002 targets hereditary angioedema. Additionally, Intellia is developing various other liver-focused therapies for conditions such as hemophilia A and B, hyperoxaluria Type 1, and alpha-1 antitrypsin deficiency. Its ex vivo (processed outside the body) pipeline features NTLA-5001, a candidate for acute myeloid leukemia. The company is also progressing proprietary programs focused on creating engineered cell therapies to address diverse oncological and autoimmune disorders. At the core of Intellia's technology is the Clustered, Regularly Interspaced Short Palindromic Repeats/CRISPR associated 9 (CRISPR/Cas9) system. Intellia Therapeutics, Inc. has established multiple licensing and collaboration agreements. These include a partnership with Novartis Institutes for BioMedical Research, Inc. to engineer hematopoietic stem cells for treating sickle cell disease, and a co-development agreement with Regeneron Pharmaceuticals, Inc. for potential products against hemophilia A and B. The company also collaborates with Ospedale San Raffaele and holds a strategic alliance with SparingVision SAS to develop novel genomic medicines for ocular diseases, leveraging CRISPR/Cas9 technology. The company, initially known as AZRN, Inc., was founded in 2014 and operates from its headquarters in Cambridge, Massachusetts.