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Intellectia

NTLA News

Analysis of Intellia Therapeutics' Stock Price Recovery

2d agoFool

Intellia Therapeutics Overcomes Regulatory Setback

2d agoNASDAQ.COM

Cathie Wood's Intellia Therapeutics Surges 47%: Is It Too Late to Invest?

2d agoYahoo Finance

Wall Street Analysts Adjust Ratings

6d agoBenzinga

Cathie Wood Continues to Add to Growth Stock Positions

Mar 03 2026Fool

Wall Street Analysts Adjust GE Stock Ratings

Mar 03 2026Benzinga

Intellia Presents New Research at AAAAI Meeting

Mar 03 2026Newsfilter

Intellia Therapeutics FDA Lifts Clinical Hold on Nexizuran Trials

Mar 02 2026seekingalpha

NTLA Events

03/03 07:50
Intellia Therapeutics Presents Hereditary Angioedema Study Results
Intellia Therapeutics announced details about its presentation of four posters at the 2026 American Academy of Allergy, Asthma & Immunology Annual Meeting, AAAAI, that took place this past weekend in Philadelphia, Pennsylvania. Title: Long-Term Durability and Safety of Lonvoguran Ziclumeran 50 mg in Patients with Hereditary Angioedema: Across the 32 patients, the mean monthly attack rate was consistently less than or equal to0.2, representing a mean reduction of 96% in HAE attacks from baseline through last follow-up. Of the 32 patients, 31 were both attack-free and LTP-free as of the data cutoff, with the attack-free and LTP-free periods ranging from 2 months to 3 years with follow-up ongoing. Title: Evolving Treatment Goals to Achieve Freedom from Attacks and Long-Term Prophylaxis Following a One-Time Treatment with Lonvoguran Ziclumeran: Of the 28 patients with greater than6 months of follow-up after receiving a one-time 50 mg treatment of lonvo-z in a pooled Phase 1/2 analysis, 86% were attack-free and LTP-free for greater than6 months, a timeframe suggested by patients to be clinically meaningful. Title: Quantitative Systems Biology Modeling Estimates Extent of Excessive Kallikrein Generation in Hereditary Angioedema Patients: In this model, an 85% reduction in prekallikrein was shown to reduce peak free kallikrein and peak bradykin to near normal ranges. This level of reduction in prekallikrein is consistent with what has been observed clinically with a 50 mg dose of lonvo-z

NTLA Monitor News

Intellia's FDA Approval Boosts Clinical Trial for Nex-z

Mar 03 2026

Intellia's Shares Surge as FDA Lifts Hold on Nexiguran Trial

Mar 02 2026

FDA Lifts Clinical Hold on Intellia's Phase 3 Trial

Jan 28 2026

Intellia Therapeutics shares surge amid market gains

Jan 27 2026

ARK Invest Acquires Shares of Intellia, Boosting Stock Price

Jan 22 2026

NTLA Earnings Analysis

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