{"id":790334,"date":"2024-11-25T07:34:06","date_gmt":"2024-11-25T12:34:06","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/"},"modified":"2024-11-25T07:34:06","modified_gmt":"2024-11-25T12:34:06","slug":"intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/","title":{"rendered":"Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy"},"content":{"rendered":"
\n

CAMBRIDGE, Mass, Nov. 25, 2024 (GLOBE NEWSWIRE) — Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative Medicine Advanced Therapy (RMAT) designation to nexiguran ziclumeran (nex-z, also known as NTLA-2001) for the treatment of hereditary transthyretin (ATTR) amyloidosis with polyneuropathy (ATTRv-PN). Nex-z is an in vivo<\/em>\u00a0CRISPR-based investigational\u00a0therapy designed as a single-dose treatment to inactivate the\u00a0TTR<\/em>\u00a0gene and thereby prevent the production of TTR protein for the treatment of ATTR amyloidosis. Development and commercialization of nex-z is led by Intellia as part of a multi-target collaboration with Regeneron.<\/p>\n

\u201cThis RMAT designation underscores the transformative potential of nex-z, our investigational in vivo<\/em> CRISPR-based gene editing therapy for those living with hereditary ATTR amyloidosis with polyneuropathy,\u201d said Intellia President and Chief Executive Officer John Leonard, M.D. \u201cIt was granted following the FDA\u2019s review of our compelling interim Phase 1 data that indicated our one-time treatment led to rapid, deep and durable TTR reduction, which is expected to halt and potentially reverse the disease. We look forward to working closely with the FDA to bring this potential paradigm-shifting therapy to patients as quickly as possible.\u201d<\/p>\n

The RMAT designation was established under the 21st<\/sup> Century Cures Act to expedite the development and review of promising therapeutic candidates, including genetic therapies, that are intended to treat, modify, reverse or cure a serious or life-threatening disease. RMAT designation includes benefits, such as early interactions with the FDA, including discussions on surrogate or intermediate endpoints that could potentially support accelerated approval and satisfy post-approval requirements, and potential priority review of a product\u2019s biologics license application (BLA).<\/p>\n

This RMAT designation is the third special regulatory designation received by Intellia for nex-z. Nex-z was also granted Orphan Drug Designation by the U.S. FDA and European Union Orphan Drug Designation by the European Commission.<\/p>\n

\n About nexiguran ziclumeran (nex-z, also known as NTLA-2001)<\/strong>
\n
Based on Nobel Prize-winning CRISPR\/Cas9 technology, nex-z has the potential to become the first one-time treatment for transthyretin (ATTR) amyloidosis. Nex-z is designed to inactivate the\u00a0TTR<\/em>\u00a0gene that encodes for the transthyretin (TTR) protein. Interim Phase 1 clinical data showed the administration of nex-z led to consistent, deep and long-lasting TTR reduction. Intellia leads development and commercialization of nex-z as part of a multi-target discovery, development and commercialization\u00a0collaboration\u00a0with Regeneron.<\/p>\n

\n About Transthyretin (ATTR) Amyloidosis<\/strong>
\n
Transthyretin amyloidosis, or ATTR amyloidosis, is a rare, progressive and fatal disease. Hereditary ATTR (ATTRv) amyloidosis occurs when a person is born with mutations in the TTR gene, which causes the liver to produce structurally abnormal transthyretin (TTR) protein with a propensity to misfold. These damaged proteins build up as amyloid in the body, causing serious complications in multiple tissues, including the heart, nerves and digestive system. ATTRv amyloidosis predominantly manifests as polyneuropathy (ATTRv-PN), which can lead to nerve damage, or cardiomyopathy (ATTRv-CM), which can lead to heart failure. Some individuals without the genetic mutation produce non-mutated, or wild-type TTR proteins that become unstable over time, misfolding and aggregating in disease-causing amyloid deposits. This condition, called wild-type ATTR (ATTRwt) amyloidosis, primarily affects the heart. There are an estimated 50,000 people worldwide living with ATTRv amyloidosis and between 200,000 and 500,000 people with ATTRwt amyloidosis. There is no known cure for ATTR amyloidosis and currently available medications are limited to slowing accumulation of misfolded TTR protein.<\/p>\n

\n About Intellia Therapeutics<\/strong>
\n
Intellia Therapeutics, Inc. (NASDAQ:NTLA) is a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies. The company\u2019s\u00a0in vivo<\/em>\u00a0programs use CRISPR to enable precise editing of disease-causing genes directly inside the human body. Intellia\u2019s\u00a0ex vivo<\/em>\u00a0programs use CRISPR to engineer human cells outside the body for the treatment of cancer and autoimmune diseases. Intellia\u2019s deep scientific, technical and clinical development experience, along with its people, is helping set the standard for a new class of medicine. To harness the full potential of gene editing, Intellia continues to expand the capabilities of its CRISPR-based platform with novel editing and delivery technologies. Learn more at\u00a0intelliatx.com<\/a> and follow us @intelliatx<\/a>.<\/p>\n

\n Forward-Looking Statements<\/strong>
\n
This press release contains \u201cforward-looking statements\u201d of\u00a0Intellia Therapeutics, Inc.\u00a0(\u201cIntellia\u201d or the \u201cCompany\u201d) 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\u2019s beliefs and expectations regarding: the safety, efficacy, success and advancement of its clinical program for nexiguran ziclumeran (nex-z, also known as NTLA-2001) for the treatment of hereditary transthyretin (ATTR) amyloidosis with polyneuropathy (ATTRv-PN) pursuant to its clinical trial applications and investigational new drug application, including the potential of nex-z to halt and potentially reverse the disease and its potential to offer a paradigm-shifting treatment option for patients with ATTRv-PN.<\/p>\n

Any forward-looking statements in this press release are based on management\u2019s 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: risks related to Intellia\u2019s ability to protect and maintain its intellectual property position; risks related to valid third party intellectual property; risks related to Intellia\u2019s relationship with third parties, including its licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; and uncertainties related to the authorization, initiation, enrollment and conduct of studies and other development requirements for its product candidates, including nex-z; risks related to the results of preclinical or clinical studies, including that they may not be positive or predictive of future results; the risk that one or more of Intellia\u2019s product candidates, including nex-z, will not be successfully developed and commercialized; and risks related to Intellia\u2019s reliance on collaborations, including that its collaboration with Regeneron will not continue or will not be successful. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Intellia\u2019s actual results to differ from those contained in the forward-looking statements, see the section entitled \u201cRisk Factors\u201d in Intellia\u2019s most recent annual report on Form 10-K as well as discussions of potential risks, uncertainties, and other important factors in Intellia\u2019s other filings with the\u00a0Securities and Exchange Commission, including its quarterly report on Form 10-Q. All\u00a0information 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.<\/p>\n

\n
\n Intellia Contacts:<\/em>
\n <\/strong>\n <\/p>\n

\n Investors:<\/strong>
\n
Lina Li
Senior Director
Investor Relations and Corporate Communications
lina.li@intelliatx.com<\/a><\/p>\n

\n Media:<\/strong>
\n
Matt Crenson
Ten Bridge Communications
media@intelliatx.com<\/a>
mcrenson@tenbridgecommunications.com<\/a><\/p>\n

\"\"
\n
\n \"\"\n <\/div>\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

CAMBRIDGE, Mass, Nov. 25, 2024 (GLOBE NEWSWIRE) — Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative Medicine Advanced Therapy (RMAT) designation to nexiguran ziclumeran (nex-z, also known as NTLA-2001) for the treatment of hereditary transthyretin (ATTR) amyloidosis with polyneuropathy (ATTRv-PN). Nex-z is an in vivo\u00a0CRISPR-based investigational\u00a0therapy designed as a single-dose treatment to inactivate the\u00a0TTR\u00a0gene and thereby prevent the production of TTR protein for the treatment of ATTR amyloidosis. Development and commercialization of nex-z is led by Intellia as part of a multi-target collaboration with Regeneron. \u201cThis RMAT designation underscores the transformative potential of nex-z, our investigational in vivo … <\/p>\n

Continue reading “Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-790334","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nIntellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"CAMBRIDGE, Mass, Nov. 25, 2024 (GLOBE NEWSWIRE) — Intellia Therapeutics, Inc. 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(NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative Medicine Advanced Therapy (RMAT) designation to nexiguran ziclumeran (nex-z, also known as NTLA-2001) for the treatment of hereditary transthyretin (ATTR) amyloidosis with polyneuropathy (ATTRv-PN). Nex-z is an in vivo\u00a0CRISPR-based investigational\u00a0therapy designed as a single-dose treatment to inactivate the\u00a0TTR\u00a0gene and thereby prevent the production of TTR protein for the treatment of ATTR amyloidosis. Development and commercialization of nex-z is led by Intellia as part of a multi-target collaboration with Regeneron. \u201cThis RMAT designation underscores the transformative potential of nex-z, our investigational in vivo … Continue reading \"Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/","og_site_name":"Market Newsdesk","article_published_time":"2024-11-25T12:34:06+00:00","og_image":[{"url":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTI3ODkwNSM2NTk3NzkwIzIwMjkyMDE=","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"6 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy","datePublished":"2024-11-25T12:34:06+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/"},"wordCount":1154,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTI3ODkwNSM2NTk3NzkwIzIwMjkyMDE=","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/intellia-therapeutics-announces-fda-regenerative-medicine-advanced-therapy-rmat-designation-granted-to-nexiguran-ziclumeran-nex-z-for-the-treatment-of-hereditary-transthyretin-attr-amyloidosis-w\/","name":"Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Hereditary Transthyretin (ATTR) Amyloidosis with Polyneuropathy - 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