MARKET

NTLA

NTLA

Intellia Therape
NASDAQ
20.76
+0.74
+3.70%
After Hours: 20.34 -0.42 -2.02% 19:51 04/26 EDT
OPEN
20.11
PREV CLOSE
20.02
HIGH
20.99
LOW
19.37
VOLUME
1.03M
TURNOVER
0
52 WEEK HIGH
47.48
52 WEEK LOW
19.37
MARKET CAP
2.00B
P/E (TTM)
-3.8298
1D
5D
1M
3M
1Y
5Y
Intellia (NTLA) to Report Q1 Earnings: What's in the Cards?
NASDAQ · 2d ago
Wedbush Reiterates Neutral on Intellia Therapeutics, Maintains $29 Price Target
Benzinga · 4d ago
Weekly Report: what happened at NTLA last week (0415-0419)?
Weekly Report · 5d ago
Tracking Cathie Wood's ARK Invest 13F Portfolio - Q1 2024 Update
Seeking Alpha · 04/19 07:54
Intellia Therapeutics Welcomes New Principal Accounting Officer
TipRanks · 04/15 20:32
Weekly Report: what happened at NTLA last week (0408-0412)?
Weekly Report · 04/15 12:17
Analysts Offer Insights on Healthcare Companies: Pacira Pharmaceuticals (PCRX), Legend Biotech (LEGN) and Intellia Therapeutics (NTLA)
Pacira Pharmaceuticals (PCRX), Legend Biotech and Intellia Therapeutics (NTLA) have been recommended by 3 analysts with bullish sentiments. RBC Capital maintained a Buy rating on Pacira and Cantor Fitzgerald initiated coverage on the 3 Healthcare stocks. The analysts are bullish on the Healthcare sector as a whole.
TipRanks · 04/09 01:50
Weekly Report: what happened at NTLA last week (0401-0405)?
Weekly Report · 04/08 12:23
More
About NTLA
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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