Intellia Therapeutics, Inc

NTLA

Intellia Therapeutics, Inc. is a biotechnology company focused on developing gene-editing therapies using CRISPR-Cas9 technology. Founded to advance precise genetic modifications for treating genetic diseases and other medical conditions, the company aims to deliver transformative medicines through both in vivo and ex vivo approaches.

$15.90 -0.19 (-1.19%)
🚫 Intellia Therapeutics, Inc does not pay dividends

Company News

Genome Editing Market Forecast to Reach $23.6 Billion by 2031 Registering 16.6% CAGR: Insights Into Technology and Investment Trends
GlobeNewswire Inc. • Researchandmarkets.Com • January 22, 2026

The global genome editing market is projected to grow from $9.39 billion in 2025 to $23.66 billion by 2031, driven by increased funding, CRISPR advancements, and AI integration. However, off-target effects and regulatory hurdles pose significant challenges. Key developments include AI-enhanced editing systems achieving 95% reduction in off-target...

Gene Editing Market Size to Surpass USD 42.13 Billion by 2034
GlobeNewswire Inc. • Nova One Advisor • November 4, 2025

The global gene editing market is projected to grow from $11.29 billion in 2025 to $42.13 billion by 2034, with a CAGR of 15.76%. North America dominates the market, while CRISPR-Cas9 technology leads in market share. Key drivers include potential medical and agricultural applications.

Meet the Beaten-Down Biotech Stock Cathie Wood Loves and Wall Street Says May Soar More Than 130%
The Motley Fool • Prosper Junior Bakiny • November 2, 2025

Intellia Therapeutics, a biotech company developing gene-editing therapies for rare diseases, faces significant risks after pausing clinical trials due to a patient experiencing liver damage. Despite potential blockbuster drug candidates, the stock's future remains uncertain.

CRISPR Therapies Clinical Trial Pipeline Shows Potential with Active Contributions from 25+ Key Companies | DelveInsight
GlobeNewswire Inc. • Delveinsight • October 2, 2025

CRISPR therapies are showing significant potential with over 25 key companies developing 30+ pipeline therapies targeting genetic disorders, with promising clinical trials across various disease areas.

Intellia Therapeutics Announces Positive Longer-Term Phase 1 Data for Nexiguran Ziclumeran (nex-z) in Patients with Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy
Benzinga • Globe Newswire • September 25, 2025

Intellia Therapeutics reported positive Phase 1 trial results for its gene editing therapy nex-z, showing sustained transthyretin protein reductions and potential clinical improvements in patients with hereditary ATTR amyloidosis. The company expects to complete Phase 3 trial enrollment in 2026 and potentially file for biologics license by 2028.

Related Companies