{"id":752885,"date":"2023-05-01T07:16:49","date_gmt":"2023-05-01T11:16:49","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/"},"modified":"2023-05-01T07:16:49","modified_gmt":"2023-05-01T11:16:49","slug":"minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/","title":{"rendered":"Minerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia"},"content":{"rendered":"

\nFDA grants appeal and files NDA
\n<\/h2>\n
\n

BURLINGTON, Mass., May 01, 2023 (GLOBE NEWSWIRE) — Minerva Neurosciences, Inc.<\/a> (Nasdaq: NERV), a clinical-stage biopharmaceutical company focused on the development of therapies to treat central nervous system (CNS) disorders, today announced that the U.S. Food and Drug Administration (FDA) filed the Company\u2019s New Drug Application (NDA) for roluperidone for the treatment of negative symptoms in patients with schizophrenia on April 27, 2023. The decision to file the NDA follows the Company\u2019s request for formal dispute resolution and appeal of FDA\u2019s October 2022 refuse to file letter. The issues cited in the refuse-to-file decision included those discussed at the type C meeting in April 2022.\u00a0In granting the appeal, the FDA deciding official agreed with the Company that the issues cited in the refuse-to-file decision\u00a0should be considered during FDA\u2019s review of the NDA.<\/p>\n

\u201cWe thank the FDA for its thoughtful review and consideration of our materials submitted during the formal dispute resolution process. We look forward to continuing to work with the FDA with the ultimate goal of obtaining approval of roluperidone as the first approved treatment for negative symptoms of schizophrenia for the benefit of patients, their families, caregivers, and physicians,\u201d said Dr. Remy Luthringer, Executive Chairman and Chief Executive Officer of Minerva.<\/p>\n

\u201cNegative symptoms are a major source of disability in people with schizophrenia and there have been no approved treatments to date. An approved treatment for negative symptoms could revolutionize the treatment of schizophrenia and would certainly have a major impact on the quality of life of the millions of people affected with this disease,\u201d said Dr. Philip Harvey, Leonard M. Miller Professor\u00a0of Psychiatry and Behavioral Sciences and Director of the\u00a0Division of Psychology\u00a0at the\u00a0University of Miami Miller School of Medicine.<\/p>\n

\n About Schizophrenia and Negative Symptoms<\/strong>
\n
Schizophrenia is a chronic, severe, and debilitating type of mental illness characterized by distortions in thinking, perception, emotions, language, sense of self and behavior. Schizophrenia affects 20 million people worldwide. (World Health Organization<\/a>).<\/p>\n

Negative symptoms can cause individuals with schizophrenia to withdraw from society, become disinterested or unable to complete tasks or feel pleasure. Negative symptoms are characterized by five constructs: blunted affect, alogia, avolition, anhedonia, and asociality (Marder and Galderisi, 2017<\/a>).<\/p>\n

Negative symptoms are the main cause of the poor functional outcome of patients suffering from schizophrenia (Harvey et al., 2020<\/a>) and may also be one of the main reasons ultra-high risk adolescents may develop full blown schizophrenia (Gomes and Grace, 2017<\/a>). There are currently no treatments approved for negative symptoms of schizophrenia in the US.<\/p>\n

Minerva believes that research continues to emerge indicating that there is a large subgroup of patients with schizophrenia who have moderate to severe primary negative symptoms and minimal positive symptoms (Galderisi\u00a02021<\/a>) and have a low risk of worsening of positive symptoms even in the absence of antipsychotic treatments (Harrow\u00a02013<\/a>; Moilanen\u00a02016<\/a>;\u00a0 Murray\u00a02016<\/a>; \u00a0Wils\u00a02017<\/a>; Wunderink\u00a02013<\/a>; Landolt\u00a02016<\/a>).<\/p>\n

\n About Minerva Neurosciences<\/strong>\n <\/p>\n

\n Minerva Neurosciences, Inc.<\/strong> (Nasdaq: NERV) is a clinical-stage biopharmaceutical company focused on developing product candidates to treat central nervous system (CNS) diseases. Our goal is to transform the lives of patients with improved therapeutic options. Minerva\u2019s portfolio of compounds includes roluperidone (MIN-101), in clinical development for negative symptoms of schizophrenia, and MIN-301 for Parkinson\u2019s disease.\u00a0For more information, please visit our website.<\/a><\/p>\n

\n
\n Forward-Looking Safe Harbor Statement<\/em>
\n <\/strong>\n <\/p>\n

\n This press release contains forward-looking statements which are subject to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts, reflect management\u2019s expectations as of the date of this press release, and involve certain risks and uncertainties. These statements may be identified by words such as \u201caims,\u201d \u201canticipates,\u201d \u201cbelieves,\u201d \u201ccould,\u201d \u201cestimates,\u201d \u201cexpects,\u201d \u201cforecasts,\u201d \u201cgoal,\u201d \u201cintends,\u201d \u201cmay,\u201d \u201cplans,\u201d \u201cpossible,\u201d \u201cpotential,\u201d \u201cseeks,\u201d \u201cwill\u201d and variations of these words or similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these words. Forward-looking statements include, but are not limited to, statements herein with respect to the regulatory progress and therapeutic potential of roluperidone for the treatment of negative symptoms in patients with schizophrenia. These forward-looking statements are based on our current expectations and may differ materially from actual results due to a variety of factors including, without limitation, whether the FDA will require additional trials or data which may significantly delay and put at risk our efforts to obtain regulatory approval; whether the FDA may meet expected review timelines for our NDA; whether roluperidone will be successfully marketed if approved; management\u2019s ability to successfully achieve its goals; our ability to raise additional capital to fund our operations and corporate objectives on terms acceptable to us; general economic conditions; and other factors that are described under the caption \u201cRisk Factors\u201d in our filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K for the year ended\u00a0December 31, 2022, filed with the\u00a0Securities and Exchange Commission on March 8, 2023. Copies of reports filed with the\u00a0SEC\u00a0are posted on our website at <\/em>
\n
\n www.minervaneurosciences.com<\/em>
\n <\/a>
\n . The forward-looking statements in this press release are based on information available to us as of the date hereof, and we expressly disclaim any obligation to update any forward-looking statements, except as required by law.<\/em>\n <\/p>\n

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

\n Investor inquiries:<\/strong>
\n \n <\/p>\n

Frederick Ahlholm
Chief Financial Officer
Minerva Neurosciences, Inc.
Info@minervaneurosciences.com<\/p>\n

\n Media inquiries: <\/strong>
\n \n <\/p>\n

Helen Shik
Principal
Shik Communications LLC
Helen@ShikCommunications.com<\/p>\n

\u00a0<\/p>\n


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

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

FDA grants appeal and files NDA BURLINGTON, Mass., May 01, 2023 (GLOBE NEWSWIRE) — Minerva Neurosciences, Inc. (Nasdaq: NERV), a clinical-stage biopharmaceutical company focused on the development of therapies to treat central nervous system (CNS) disorders, today announced that the U.S. Food and Drug Administration (FDA) filed the Company\u2019s New Drug Application (NDA) for roluperidone for the treatment of negative symptoms in patients with schizophrenia on April 27, 2023. The decision to file the NDA follows the Company\u2019s request for formal dispute resolution and appeal of FDA\u2019s October 2022 refuse to file letter. The issues cited in the refuse-to-file decision included those discussed at the type C meeting in April 2022.\u00a0In granting the appeal, the FDA deciding official agreed with … <\/p>\n

Continue reading “Minerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia”<\/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-752885","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nMinerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia - 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\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Minerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"FDA grants appeal and files NDA BURLINGTON, Mass., May 01, 2023 (GLOBE NEWSWIRE) — Minerva Neurosciences, Inc. 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(Nasdaq: NERV), a clinical-stage biopharmaceutical company focused on the development of therapies to treat central nervous system (CNS) disorders, today announced that the U.S. Food and Drug Administration (FDA) filed the Company\u2019s New Drug Application (NDA) for roluperidone for the treatment of negative symptoms in patients with schizophrenia on April 27, 2023. The decision to file the NDA follows the Company\u2019s request for formal dispute resolution and appeal of FDA\u2019s October 2022 refuse to file letter. The issues cited in the refuse-to-file decision included those discussed at the type C meeting in April 2022.\u00a0In granting the appeal, the FDA deciding official agreed with … Continue reading \"Minerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/","og_site_name":"Market Newsdesk","article_published_time":"2023-05-01T11:16:49+00:00","og_image":[{"url":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODgyODc2NSM1NTY2Mjc3IzIwMDcyNDU=","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Minerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia","datePublished":"2023-05-01T11:16:49+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/"},"wordCount":899,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODgyODc2NSM1NTY2Mjc3IzIwMDcyNDU=","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/minerva-neurosciences-announces-the-nda-filing-for-roluperidone-for-the-treatment-of-negative-symptoms-in-schizophrenia\/","name":"Minerva Neurosciences Announces the NDA Filing for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia - 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