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Intellia Therapeutics Announces FDA Acceptance of Biologics License Application with Priority Review for Lonvoguran Ziclumeran (Lonvo-z) for Hereditary Angioedema (HAE)

FDA Priority Review of Intellia’s lonvo-z BLA, backed by positive Phase 3 HAELO data, could enable the first one-time in vivo CRISPR HAE therapy.

(Moderate)
(Very Positive)

Intellia Therapeutics (NTLA) received FDA acceptance and Priority Review of its Biologics License Application for lonvoguran ziclumeran (lonvo-z) for hereditary angioedema (HAE), with a PDUFA target action date of March 10, 2027.

The FDA also advised that it is not currently planning to hold an advisory committee meeting on the application. Lonvo-z is positioned, if approved, to be the world’s first in vivo CRISPR-based therapy and the only one-time treatment for HAE. The BLA is supported by the global Phase 3 HAELO trial in 80 adults and adolescents (≥16 years) with Type 1 or Type 2 HAE, evaluating a single 50 mg dose.

HAELO met its primary and all key secondary endpoints, showing an 87% reduction in mean monthly attacks versus placebo from weeks 5 to 28 (p<0.0001). During the six-month efficacy period, 62% of lonvo-z patients were attack free and HAE-therapy free, versus 11% on placebo (p<0.0001). No serious adverse events occurred in the lonvo-z arm; all treatment emergent events were mild or moderate.

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Positive

  • BLA Priority Review granted for lonvo-z with PDUFA date March 10, 2027
  • 87% reduction in mean monthly HAE attacks vs placebo (weeks 5–28, p<0.0001)
  • 62% attack- and HAE-therapy free on lonvo-z vs 11% on placebo over 6 months (p<0.0001)
  • All lonvo-z patients remained free from long-term prophylaxis therapy at Feb. 10, 2026 cutoff
  • No serious adverse events reported in the lonvo-z arm; all TEAEs mild or moderate
  • FDA is not currently planning an advisory committee for the lonvo-z BLA

Negative

  • Higher rates of infusion-related reactions, headache, fatigue, back pain, and upper respiratory tract infection vs placebo in the lonvo-z arm

Market Context

On Apr 27, 2026, NTLA recorded a 4.33% negative 24-hour reaction alongside positive Phase 3 HAELO re...
Analysis

On Apr 27, 2026, NTLA recorded a 4.33% negative 24-hour reaction alongside positive Phase 3 HAELO results, providing relevant prior market context for today’s FDA acceptance and Priority Review milestone.

Key Figures

PDUFA Target Action Date: March 10, 2027 Trial Enrollment: 80 patients Dose: 50 milligrams +3 more
PDUFA Target Action Date
March 10, 2027
Lonvo-z BLA Priority Review
Trial Enrollment
80 patients
Phase 3 HAELO trial
Dose
50 milligrams
One-time lonvo-z dose
Reduction in Mean Monthly Attacks
87%
Lonvo-z versus placebo during weeks 5 to 28
Attack- and Therapy-Free Patients
62% versus 11%
Lonvo-z versus placebo during the six-month efficacy evaluation period
Statistical Significance
p<0.0001
Primary and key secondary HAELO endpoints

Previous Clinical trial Reports

2 past events · Latest: Apr 27
Same Type 2 events
  1. Apr 27

    Phase 3 results

    24h Move
    -4.3%

    Phase 3 HAELO results showed 87% attack reduction versus placebo in 80 patients

  2. Mar 03

    Phase 1/2 data

    24h Move
    -11.9%

    Longer-term Phase 1/2 data showed durable attack and prophylaxis-free outcomes for lonvo-z

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

pdufa, biologics license application, priority review, crisper, +1 more
5 terms
pdufa regulatory
"FDA sets Prescription Drug User Fee Act (PDUFA) date"
PDUFA is the Prescription Drug User Fee Act, the U.S. law under which drug companies pay fees that fund the FDA's review of new medicines. In company news the term usually appears as the PDUFA date, the target deadline by which the FDA aims to decide on a drug application; that date tells investors when to expect the approval or rejection decision for the product.
biologics license application regulatory
"accepted the Biologics License Application (BLA)"
A biologics license application is a formal request submitted to regulatory authorities seeking approval to market a new biological medicine, such as vaccines or treatments made from living organisms. It is a comprehensive review process that evaluates the safety, effectiveness, and manufacturing quality of the product. For investors, receiving approval signals that a biological therapy can be sold to the public, potentially leading to revenue growth and market success.
priority review regulatory
"granted the BLA Priority Review"
Priority review is a regulatory fast-track that shortens the time an agency spends evaluating a drug, vaccine or medical device application so a decision comes sooner than normal. For investors, it matters because a faster review is like an express lane to market: it can speed revenue potential and reduce regulatory uncertainty, but it does not guarantee approval and still requires the product to meet safety and effectiveness standards.
crisper technical
"world’s first in vivo CRISPR-based therapy"
A type of gene‑editing technology that lets scientists precisely change DNA sequences inside living cells, like using a pair of molecular scissors guided by a map to cut and replace specific paragraphs in a huge instruction manual. Investors care because it underpins a wave of potential new therapies and biotech products, and progress or setbacks in safety, regulation, or clinical results can rapidly affect the value of companies developing related treatments.
hae medical
"one-time HAE treatment, if approved"
Hereditary angioedema (HAE) is a rare genetic disorder that causes sudden, severe swelling in tissues such as the face, throat, abdomen and limbs due to abnormal control of blood vessel leakage. It matters to investors because HAE treatments, which can be life‑saving and are often taken long‑term, represent a specialized drug market with high per‑patient revenue and regulatory, pricing and reimbursement risks similar to other rare‑disease therapies.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • FDA sets Prescription Drug User Fee Act (PDUFA) date of March 10, 2027
  • Positions lonvo-z to be the world’s first in vivo CRISPR-based therapy and the only one-time HAE treatment, if approved

CAMBRIDGE, Mass., Sept. 08, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced the U.S. Food and Drug Administration (FDA) has accepted the Biologics License Application (BLA) for lonvo-z and granted the BLA Priority Review with a PDUFA target action date of March 10, 2027. Additionally, FDA has advised the company that it is not currently planning to hold an advisory committee to discuss the application. If approved, lonvo-z would be the world’s first in vivo CRISPR-based therapy and the only one-time treatment for HAE.

“Today marks an important milestone for the patients we are committed to serving and for Intellia’s pioneering work in the field of in vivo gene editing,” said John Leonard, M.D., Intellia President and Chief Executive Officer. “Backed by compelling Phase 3 data, we believe lonvo-z could fundamentally change the way HAE is treated and are excited by its potential to become the world's first approved in vivo CRISPR-based therapy. With the FDA’s Priority Review underway, our team is well prepared to deliver this one-time treatment to patients who are waiting for new options.”

Joshua Jacobs, M.D., Medical Director, Allergy and Asthma Clinical Research, Inc., and a HAELO trial investigator, added, “HAE is an unpredictable disease that can be responsible for profound disability and place patients at risk for fatal attacks. Today’s announcement is exciting because it advances us one step closer to potentially having a one-time treatment option available for patients who continue to be burdened by this chronic disease.”

The BLA is supported by positive data from Intellia’s global Phase 3 HAELO clinical trial, which was fully enrolled with 80 patients in just nine months and was designed to evaluate the efficacy and safety of a one-time 50 milligram dose of lonvo-z in adults and adolescents aged 16 years and older with Type 1 or Type 2 HAE. HAELO met its primary and all key secondary endpoints, demonstrating an 87% reduction (p<0.0001) in mean monthly attacks for lonvo-z compared with placebo during the efficacy evaluation period (weeks 5 to 28). In addition, 62% of patients in the lonvo-z arm were entirely attack free and HAE therapy free for the six-month efficacy evaluation period, compared with 11% of patients in the placebo arm (p<0.0001). As of the February 10, 2026 data cutoff, all patients who received lonvo-z at baseline or in crossover after week 28 remained free from long-term prophylaxis therapy.

Favorable safety and tolerability data were observed for lonvo-z as of the data cutoff. The most common treatment emergent adverse events during the primary observation period (infusion through week 28) that were higher in the lonvo-z group compared to placebo were infusion-related reactions, headache, fatigue, back pain, and upper respiratory tract infection. All reported treatment emergent adverse events were mild or moderate and there were no serious adverse events observed in the lonvo-z arm.

About Lonvo-z
Based on Nobel Prize-winning CRISPR/Cas9 technology, lonvo-z has the potential to become the first one-time treatment for hereditary angioedema (HAE). Lonvo-z is an in vivo CRISPR gene editing candidate that is intended to permanently lower kallikrein by inactivating the kallikrein B1 (KLKB1) gene with a single dose that is administered in an outpatient setting. Lonvo-z has received five notable regulatory designations: Orphan Drug and Regenerative Medicine Advanced Therapy (RMAT) Designations by the U.S. Food and Drug Administration (FDA), the Innovation Passport by the U.K. Medicines and Healthcare products Regulatory Agency (MHRA), Priority Medicines (PRIME) Designation by the European Medicines Agency, as well as Orphan Drug Designation (ODD) by the European Commission.

About Hereditary Angioedema
HAE is a rare, genetic disease characterized by severe, recurring and unpredictable inflammatory attacks in various organs and tissues of the body, which can be painful, debilitating and life-threatening. It is estimated that one in 50,000 people are affected by HAE. There are preventative and on-demand treatment options to help manage the condition, including long- and short-term prophylaxis used to prevent swelling attacks. Current treatment options often include lifelong therapies, which may require chronic intravenous (IV) or subcutaneous (SC) administration as often as twice per week or daily oral administration to ensure constant pathway suppression for disease control. Despite chronic administration, breakthrough attacks may still occur. Kallikrein inhibition is a clinically validated strategy for the preventive treatment of HAE attacks.

About Intellia Therapeutics

Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease. Learn more at intelliatx.com and follow us @intelliatx.

Forward-Looking Statements

This press release contains “forward-looking statements” of Intellia Therapeutics, Inc. (“Intellia” or the “Company”) within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements regarding Intellia’s beliefs and expectations concerning: the success and advancement of its program for lonvoguran ziclumeran or “lonvo-z” (formerly known as NTLA-2002) for the treatment of hereditary angioedema (“HAE”), including its expectations regarding review and approval of its biologics license application (“BLA”) for lonvo-z, such as whether the FDA will hold an advisory committee to discuss the BLA and the timing of such review and approval based on the Prescription Drug User Fee Act ("PDUFA") target action date of March 10, 2027 for the BLA; its belief that lonvo-z could fundamentally change the way HAE is treated and has the potential to become the world's first approved in vivo CRISPR-based therapy; and its expectations regarding its preparations for and the potential success of the commercial launch of lonvo-z, if approved.

Any forward-looking statements in this press release are based on management’s current expectations and beliefs of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: uncertainties related to the conduct of clinical studies and other development and commercialization requirements for its product candidates, including lonvo-z, including risks related to the review and approval of the BLA for lonvo-z and the ability to develop and successfully commercialize lonvo-z or any of Intellia’s product candidates; risks related to Intellia’s ability to protect and maintain its intellectual property position; risks related to Intellia’s relationship with third parties, including its contract manufacturers, collaborators, licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; risks related to the results of preclinical studies or clinical studies not being predictive of future results in connection with future studies; the risk that clinical study results will not be positive; and risks related to the potential delay of planned clinical trials due to regulatory feedback or other developments. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Intellia’s actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in Intellia’s most recent annual report on Form 10-K, as well as discussions of potential risks, uncertainties, and other important factors in Intellia’s other filings with the Securities and Exchange Commission, including its recent quarterly report on Form 10-Q. All information in this press release is as of the date of the release, and Intellia undertakes no duty to update this information unless required by law.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
jason.fredette@intelliatx.com

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
mtattory@lifescicomms.com 


FAQ

What makes lonvo-z distinct among hereditary angioedema treatments?

Lonvo-z is described as a one-time, in vivo CRISPR-based therapy for hereditary angioedema. If approved, the company expects it would be the world’s first in vivo CRISPR-based therapy and the only one-time treatment option for HAE, in contrast to currently available chronic prophylactic or on-demand therapies.

What was the design of the Phase 3 HAELO trial supporting the BLA?

The global Phase 3 HAELO trial enrolled 80 patients with Type 1 or Type 2 hereditary angioedema, aged 16 years and older. It evaluated the efficacy and safety of a single 50 milligram dose of lonvo-z compared with placebo, with an efficacy evaluation period from weeks 5 to 28 and a six-month assessment of attack and HAE-therapy freedom.

Which efficacy endpoints did lonvo-z meet in the HAELO trial?

HAELO met its primary and all key secondary endpoints. These included an 87% reduction in mean monthly HAE attacks for lonvo-z versus placebo during weeks 5 to 28, and a higher proportion of patients who were entirely attack free and HAE-therapy free over the six-month efficacy period (62% on lonvo-z versus 11% on placebo, both comparisons with p<0.0001).

What safety profile was observed for lonvo-z in the HAELO trial?

As of the February 10, 2026 data cutoff, lonvo-z showed a favorable safety and tolerability profile. The most common treatment emergent adverse events with higher incidence than placebo during the primary observation period (infusion through week 28) were infusion-related reactions, headache, fatigue, back pain, and upper respiratory tract infection. All treatment emergent adverse events were mild or moderate, and there were no serious adverse events reported in the lonvo-z arm.

How did lonvo-z affect patients’ need for long-term prophylaxis therapy?

As of the February 10, 2026 data cutoff, all patients who received lonvo-z at baseline or after crossover following week 28 remained free from long-term prophylaxis therapy, indicating that none required ongoing preventive HAE treatment during the reported follow-up.

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