Intellia Therapeutics Inc (OQ:NTLA)
Business Focus: Biotechnology & Medical Research
Rain as of April 01, 2024
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Latest 10 SEC Form 4 filings for NTLA*US within the last 6 months
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Company News
Mar 18, 2024 07:30 ET
Intellia Therapeutics Announces First Patient Dosed in the Phase 3 MAGNITUDE Study of NTLA-2001 as a Single-Dose CRISPR-Based Treatment for Transthyretin Amyloidosis with Cardiomyopathy
Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced the first patient dosed in the global pivotal, Phase 3 MAGNITUDE trial of...
Feb 22, 2024 07:30 ET
Intellia Therapeutics Announces Fourth Quarter and Full-Year 2023 Financial Results and Highlights Recent Company Progress
associated lung disease, in 2024Expanding development of in vivo CRISPR-based therapies to target tissues outside of the liver; announced strategic collaboration with ReCode to develop novel gene editing therapies for cystic fibrosis Ended 2023 in a...
Valuation Ratios
Industry
Sector
Beta
1.84
--
--
Price to Sales - TTM
57.04
4.15
3.12
Price to Book - most recent quarter
1.91
2.08
2.11
Price to Cash Flow per share - TTM
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12.81
13.55
Price to Free Cash Flow per share - TTM
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27.06
23.62
Business Summary
| Sector: Healthcare | Industry: Biotechnology & Medical Research |
Intellia Therapeutics, Inc. is a clinical-stage genome editing company, which is focused on developing curative therapeutics using Clustered, Regularly Interspaced Short Palindromic Repeats/CRISPR associated 9 (CRISPR/Cas9) technology. CRISPR/Cas9 is a technology for genome editing, the process of altering selected sequences of genomic deoxyribonucleic acid. It is focused on leveraging its modular platform to advance in vivo and ex vivo therapies for diseases with high unmet need. Its lead in vivo candidate, NTLA-2001, is for the treatment of transthyretin (ATTR) amyloidosis, as well as NTLA-2002 for the treatment of hereditary angioedema (HAE) are the first CRISPR/Cas9-based therapy candidates to be administered systemically, via intravenous (IV) infusion, for precision editing of a gene in a target tissue in humans. It is also developing ex vivo applications to address immuno-oncology and autoimmune diseases.
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