{"id":832858,"date":"2025-04-02T08:32:09","date_gmt":"2025-04-02T12:32:09","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/"},"modified":"2025-04-02T08:32:09","modified_gmt":"2025-04-02T12:32:09","slug":"quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/","title":{"rendered":"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient"},"content":{"rendered":"<div class=\"mw_release\">\n<ul type=\"disc\">\n<li>\n          <em>Continued Clear Visual Evidence of Almost Completely Healed Skin After 6 weeks Treatment<\/em>\n        <\/li>\n<li>\n          <em>High Durability of Treatment Effect of QRX003 with Continuous Daily Dosing <\/em>\n        <\/li>\n<li>\n          <em>Patient Continues Not to Require Previously Necessary Medications<\/em>\n        <\/li>\n<li>\n          <em>With Patient\u2019s Pruritus Almost Completely Eliminated, Patient Continues to Experience Zero Nightly Sleep Disturbance <\/em>\n        <\/li>\n<li>\n          <em>No Adverse Events Reported from 6 Weeks of Whole Body Treatment with QRX003<\/em>\n        <\/li>\n<li>\n          <em>Approval Received to Initiate Whole Body Testing of a Second Pediatric Patient<\/em>\n        <\/li>\n<\/ul>\n<p align=\"justify\">ASHBURN, Va., April  02, 2025  (GLOBE NEWSWIRE) &#8212; Quoin Pharmaceuticals Ltd. (NASDAQ: QNRX) (the \u201cCompany\u201d or \u201cQuoin\u201d), a late clinical stage, specialty pharmaceutical company focused on the development and commercialization of therapeutic products that treat rare and orphan diseases, today announces additional highly positive clinical data from its ongoing Investigator Pediatric Netherton Syndrome (NS) study. After 6 weeks of continued whole body application of QRX003, the subject\u2019s skin remains almost completely healed demonstrating the durability of ongoing daily treatment with the product. In addition, the patient has continued to have no requirement for previously necessary medications such as antibiotics, antivirals, antihistamines and glucocorticoids. Importantly, with the patient\u2019s pruritus or itch almost completely eliminated, she continues to experience zero nightly sleep disturbances without the need for any sedating medication, marking the first continuous period of uninterrupted sleep in the patient\u2019s life. No adverse events have been reported to date after 6 weeks of whole body treatment with QRX003.<\/p>\n<p align=\"justify\">Quoin CEO Dr. Michael Myers, said, \u201cAs we continue to monitor the progress of this first patient to receive whole body application with QRX003, we are very pleased to announce that after 6 weeks of dosing we are seeing continued positive improvement and the patient\u2019s skin is almost completely healed now. The patient continues to remain off previously needed medications including antihistamines, antivirals, and glucocorticoids, and she has not needed any antibiotics in the 6 weeks since the initiation of dosing with QRX003. Very importantly also, with her pruritus almost completely eliminated, the patient is still experiencing zero nightly sleep disturbances without the need for any sedating medications. For a majority of Netherton Syndrome patients, the continuous presence of chronically debilitating pruritus is the worst symptom of this disease and it severely impacts their ability to sleep or to even sit still for any period of time. Often heavy sedation is required to allow patients to sleep and sit still, which in turn has a major negative impact on their quality of life. The almost complete healing of the skin and the elimination of this chronically debilitating pruritus provides strong clinical evidence that QRX003 is successfully tackling the root causes of this disease and not merely providing symptomatic relief. Furthermore, I am very pleased to report that no adverse events have been reported after six full weeks of whole-body application of QRX003. Based on these positive results, approval has been received to initiate whole body application of QRX003 to a second pediatric Netherton patient. Testing is expected to commence in just a few weeks and we look forward to providing updates on both patients progress as we continue with our plans to further expand this study to include additional pediatric subjects.\u201d<\/p>\n<p align=\"justify\">\n        <strong>About Netherton Syndrome<\/strong><br \/>\n        <br \/>Netherton Syndrome, a form of Ichthyosis, is a rare hereditary skin disorder caused by a mutation in the SPINK5 gene (serine protease inhibitor, Kazal Type 5) that leads to severe skin barrier defects and recurring infections, as well as a pronounced predisposition to allergies, asthma, and eczema. Patients often suffer from severe dehydration, chronic skin inflammation and stunted growth. Currently, there is no cure for Netherton Syndrome, nor are there any approved therapeutic treatments.<\/p>\n<p align=\"justify\">\n        <strong>About QRX003<\/strong><br \/>\n        <br \/>QRX003 is a topical lotion formulated with a proprietary delivery technology that contains a broad-spectrum serine protease inhibitor, whose mechanism of action is intended to perform the function of a specific protein called LEKTI. The absence of LEKTI in Netherton patients leads to excessive skin shedding, resulting in a highly porous and compromised skin barrier. QRX003 is designed to promote a more normalized skin-shedding process and the formation of a stronger and more effective skin barrier. For more information about Quoin\u2019s current clinical trials please visit: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=u4DgkJzf6Zl4M15-Ra-vrpqHsgjXaMtbDLJlkiuTII9tSf_LGEa6Q-LCg-L1hHTIxZaQKst431WsLKTkJDfcu67hmlaK8qsyJlCWIIwSkBbmPHMduO45UmkdckbGb5naG2UNjZNpWYZzi1Tc2MATcpzzBFNEJBnbnL9kYJUxO-g=\" rel=\"nofollow\" target=\"_blank\">https:\/\/www.nethertonsyndromeclinicaltrials.com\/<\/a><\/p>\n<p align=\"justify\">\n        <strong>About Quoin Pharmaceuticals Ltd.<\/strong><br \/>\n        <br \/>Quoin Pharmaceuticals Ltd. is a late clinical-stage specialty pharmaceutical company focused on developing and commercializing therapeutic products that treat rare and orphan diseases. We are committed to addressing unmet medical needs for patients, their families, communities and care teams. Quoin\u2019s innovative pipeline comprises four products in development that collectively have the potential to target a broad number of rare and orphan indications, including Netherton Syndrome, Peeling Skin Syndrome, SAM Syndrome,\u00a0 Palmoplantar Keratoderma, Scleroderma, Epidermolysis Bullosa, Microcystic Lymphatic Malformations, Venous Malformations, Angiofibroma and others. For more information, visit: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=zPc3mMm8W0kf6XLTmxukqcfam8y6x5HZ0k49l_ju2rGqzUXUvrGIfE4PkeP4Qyo5ZyyrlxpvhNCjGZLwMxwrCEG1Rio-txXuM3ggyvKE6Ts=\" rel=\"nofollow\" target=\"_blank\">www.quoinpharma.com<\/a> or <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=zMWy9_uyEocfuX9_XULFx1Ly80ne8RMBvp0qelw26R_93blmmqD0-J4BXsEkmqWpN5Z05C45z0QDSG_0Mie4AZIJjpPCwm2QbKJNbb1E5aBGKTftTgTvGb-N19_EVoSgWQIPhnK-go7Of3an1so1AalHOPRHNEbyUqd_xzI8M5AMwqxt7nDqimKcT7bgV01rrOl2I-_DjLj-fYoZSxQK3r1i1meArKTQk9yyp1AmOPtiC5vVmClGNyYyOH9BmAOJ9jZUIbNHQzFWpEGB-5C7-w==\" rel=\"nofollow\" target=\"_blank\">LinkedIn<\/a> for updates.<\/p>\n<p align=\"justify\">\n        <strong>Cautionary Note Regarding Forward Looking Statements<\/strong><br \/>\n        <br \/>The Company cautions that statements in this press release that are not descriptions of historical facts are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words referencing future events or circumstances, such as \u201cexpect,\u201d \u201cintend,\u201d \u201chope,\u201d \u201cplan,\u201d \u201cpotential,\u201d \u201canticipate,\u201d \u201clook forward,\u201d \u201cbelieve,\u201d \u201cmay,\u201d and \u201cwill,\u201d among others. All statements that reflect the Company\u2019s expectations, assumptions, projections, beliefs, or opinions about the future, other than statements of historical fact, are forward-looking statements, including, without limitation, statements relating to: the potential efficacy of QRX003 as a treatment for Netherton Syndrome; testing expected to commence in a few weeks on a second pediatric patient; continue with our plans to further expand this study to include additional pediatric subjects; and Quoin\u2019s products in development collectively having the potential to target a broad number of rare and orphan indications, including Netherton Syndrome, Peeling Skin Syndrome, SAM Syndrome,\u00a0 Palmoplantar Keratoderma, Scleroderma, Epidermolysis Bullosa, Microcystic Lymphatic Malformations, Venous Malformations, Angiofibroma and others. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. These forward-looking statements are based upon the Company\u2019s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties including, but not limited to, the Company\u2019s ability to deliver a safe and effective treatment for Netherton Syndrome; whether the Company\u2019s studies successfully generate data that is sufficiently robust and comprehensive to support an NDA filing for QRX003 as an approved treatment for Netherton Syndrome; and other factors discussed in the Company\u2019s Annual Report on Form 10-K for the year ended December 31, 2024 and in other filings the Company has made and may make with the SEC in the future. One should not place undue reliance on these forward-looking statements, which speak only as of the date on which they were made. The Company undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as may be required by law.<\/p>\n<p align=\"justify\">\n        <strong>For further information, contact:<\/strong><br \/>\n        <br \/>Quoin Pharmaceuticals Ltd.<br \/>Michael Myers, Ph.D., CEO<br \/>mmyers@quoinpharma.com<\/p>\n<p align=\"justify\">\n        <strong>Investor Relations<\/strong><br \/>\n        <br \/>PCG Advisory<br \/>Jeff Ramson<br \/>jramson@pcgadvisory.com<br \/>(646) 863-6341<\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTQxNTU0OSM2ODQ3MTQ3IzIyMDk0NTc=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/MjM0NDQ2YzAtOWUwNy00YjNkLWEyN2YtN2Y2NmE0MjFiNDVhLTEyMjEwMTAtMjAyNS0wNC0wMi1lbg==\/tiny\/Quoin-Pharmaceuticals-Inc-.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Continued Clear Visual Evidence of Almost Completely Healed Skin After 6 weeks Treatment High Durability of Treatment Effect of QRX003 with Continuous Daily Dosing Patient Continues Not to Require Previously Necessary Medications With Patient\u2019s Pruritus Almost Completely Eliminated, Patient Continues to Experience Zero Nightly Sleep Disturbance No Adverse Events Reported from 6 Weeks of Whole Body Treatment with QRX003 Approval Received to Initiate Whole Body Testing of a Second Pediatric Patient ASHBURN, Va., April 02, 2025 (GLOBE NEWSWIRE) &#8212; Quoin Pharmaceuticals Ltd. (NASDAQ: QNRX) (the \u201cCompany\u201d or \u201cQuoin\u201d), a late clinical stage, specialty pharmaceutical company focused on the development and commercialization of therapeutic products that treat rare and orphan diseases, today announces additional highly positive clinical data from its ongoing &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient&#8221;<\/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-832858","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient - 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\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Continued Clear Visual Evidence of Almost Completely Healed Skin After 6 weeks Treatment High Durability of Treatment Effect of QRX003 with Continuous Daily Dosing Patient Continues Not to Require Previously Necessary Medications With Patient\u2019s Pruritus Almost Completely Eliminated, Patient Continues to Experience Zero Nightly Sleep Disturbance No Adverse Events Reported from 6 Weeks of Whole Body Treatment with QRX003 Approval Received to Initiate Whole Body Testing of a Second Pediatric Patient ASHBURN, Va., April 02, 2025 (GLOBE NEWSWIRE) &#8212; Quoin Pharmaceuticals Ltd. (NASDAQ: QNRX) (the \u201cCompany\u201d or \u201cQuoin\u201d), a late clinical stage, specialty pharmaceutical company focused on the development and commercialization of therapeutic products that treat rare and orphan diseases, today announces additional highly positive clinical data from its ongoing &hellip; Continue reading &quot;Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2025-04-02T12:32:09+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTQxNTU0OSM2ODQ3MTQ3IzIyMDk0NTc=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"6 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient\",\"datePublished\":\"2025-04-02T12:32:09+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\\\/\"},\"wordCount\":1217,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTQxNTU0OSM2ODQ3MTQ3IzIyMDk0NTc=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\\\/\",\"name\":\"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient - 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Market Newsdesk","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/","og_locale":"en_US","og_type":"article","og_title":"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient - Market Newsdesk","og_description":"Continued Clear Visual Evidence of Almost Completely Healed Skin After 6 weeks Treatment High Durability of Treatment Effect of QRX003 with Continuous Daily Dosing Patient Continues Not to Require Previously Necessary Medications With Patient\u2019s Pruritus Almost Completely Eliminated, Patient Continues to Experience Zero Nightly Sleep Disturbance No Adverse Events Reported from 6 Weeks of Whole Body Treatment with QRX003 Approval Received to Initiate Whole Body Testing of a Second Pediatric Patient ASHBURN, Va., April 02, 2025 (GLOBE NEWSWIRE) &#8212; Quoin Pharmaceuticals Ltd. (NASDAQ: QNRX) (the \u201cCompany\u201d or \u201cQuoin\u201d), a late clinical stage, specialty pharmaceutical company focused on the development and commercialization of therapeutic products that treat rare and orphan diseases, today announces additional highly positive clinical data from its ongoing &hellip; Continue reading \"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/","og_site_name":"Market Newsdesk","article_published_time":"2025-04-02T12:32:09+00:00","og_image":[{"url":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTQxNTU0OSM2ODQ3MTQ3IzIyMDk0NTc=","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\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient","datePublished":"2025-04-02T12:32:09+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/"},"wordCount":1217,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTQxNTU0OSM2ODQ3MTQ3IzIyMDk0NTc=","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/quoin-pharmaceuticals-announces-additional-positive-whole-body-clinical-data-from-ongoing-pediatric-netherton-syndrome-study-and-approval-to-initiate-testing-of-a-second-pediatric-pa\/","name":"Quoin Pharmaceuticals Announces Additional Positive \u2018Whole Body\u2019 Clinical Data from Ongoing Pediatric Netherton Syndrome Study and Approval to Initiate Testing of a Second Pediatric Patient - 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