{"id":951542,"date":"2026-04-15T08:21:56","date_gmt":"2026-04-15T12:21:56","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\/"},"modified":"2026-04-15T08:21:56","modified_gmt":"2026-04-15T12:21:56","slug":"medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\/","title":{"rendered":"Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression"},"content":{"rendered":"<h2>\nUpdated Safety, Efficacy, and Clinical Data Supports Teverelix as Potentially the First Long-Acting Injectable GnRH Antagonist Across Multiple Indications in Women\u2019s Health<br \/>\n<\/h2>\n<div class=\"mw_release\">\n<p align=\"justify\">PHILADELPHIA, April  15, 2026  (GLOBE NEWSWIRE) &#8212; Medicus Pharma Ltd. (NASDAQ: MDCX) (&#8220;Medicus&#8221; or the &#8220;Company&#8221;), a biotech\/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced it will present new Phase 1 clinical data on <strong>Teverelix<\/strong>, its investigational long-acting gonadotropin-releasing hormone (GnRH) antagonist, at the\u00a0<strong>American Association of Clinical Endocrinology Annual Meeting 2026 (AACE 2026)<\/strong> on April 22-24th in Las Vegas, Nevada.<\/p>\n<p align=\"justify\">Teverelix is being developed for hormone-driven conditions, with potential applications in women\u2019s health, including endometriosis and uterine fibroids.<\/p>\n<p align=\"justify\">Faisal Mehmud, MD, MRCP, the Company\u2019s Chief Medical Officer, will present the poster, titled\u00a0<strong><em>\u201cEvaluation of Teverelix, a Long-Acting GnRH Antagonist: Pharmacokinetics, Pharmacodynamics, Bone Turnover and Safety in Two Phase I Studies in Healthy Female Volunteer.\u201d<\/em><\/strong>\u00a0 The poster session will be on April 24th at 11:40 AM PT.<\/p>\n<p align=\"justify\">The poster presentation will highlight findings derived from two Phase I studies (TEVERELIX HFV1 and HFV2) conducted in Germany, enrolling a total of\u00a0<strong>48 healthy premenopausal women<\/strong>\u00a0evaluating single-dose subcutaneous administration of Teverelix.\u00a0<\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <u>Key Clinical Findings:<\/u><br \/>\n        <\/strong>\n      <\/p>\n<ul type=\"disc\">\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">\n          <strong>Predictable, dose-dependent estradiol suppression<\/strong><br \/>\n          <br \/>Teverelix demonstrated consistent and reversible suppression of estradiol (E2), with some subjects reaching levels within the clinically relevant\u00a0<em>Barbieri therapeutic window<\/em>\u00a0(~30-50 pg\/mL), supporting the potential for efficacy with improved tolerability.  <\/p>\n<ul type=\"circle\">\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\"><strong>Long-acting pharmacokinetics supporting infrequent dosing. PK profile consistent with a depot formulation, with rapid initial absorption and sustained exposure, supporting the potential for infrequent dosing strategies. <\/strong>Rapid initial absorption (Tmax ~0.5-2 hours)<\/li>\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">Sustained exposure with a secondary peak at 1\u20133 weeks<\/li>\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">Terminal half-life of approximately\u00a0<strong>14-23 days<\/strong><\/li>\n<\/ul>\n<\/li>\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">\n          <strong>Favorable bone turnover profile<\/strong><br \/>\n          <br \/>Bone biomarkers (DPD and NTx) remained within normal ranges with \u226410% change at Day 29.<\/li>\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">\n          <strong>Well tolerated with acceptable safety profile<\/strong><br \/>\n          <br \/>No unexpected safety signals observed across both studies.<\/li>\n<\/ul>\n<p align=\"justify\">The Company believes these Phase I findings provide a\u00a0strong mechanistic and pharmacologic foundation\u00a0for patient-based studies supporting\u00a0long-acting dosing strategies across indications, which may enable a\u00a0platform-based development strategy spanning multiple therapeutic areas.<\/p>\n<p align=\"justify\">For more information and to view the Company\u2019s abstract, visit the AACE 2026 website <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=PC99AZJJhM-OgGN5ggFe-Ydmj59gM_zMYHBuU_AfGAgCJCZ7wOpDoTTVz99i66qc_yG2ed9kd67EKcvAvPnGng==\" rel=\"nofollow\" target=\"_blank\">here<\/a>.<\/p>\n<p align=\"justify\">https:\/\/aace2026.d365.events\/education\/posters\/41c0e4cf-130f-46be-8910-0d7a1b2a8dc1<\/p>\n<p align=\"justify\">\n        <strong>Strategic Expansion: Precision Medicine Approach in Women\u2019s Health<\/strong>\n      <\/p>\n<p align=\"justify\">The Company is exploring the development of Teverelix into\u00a0<strong>symptomatic endometriosis<\/strong>, a high-burden, estrogen-dependent condition with significant unmet need.\u00a0<\/p>\n<p align=\"justify\">This program is being planned to be developed in collaboration with\u00a0<strong>Omics Labs<\/strong>\u00a0in the\u00a0<strong>United Arab Emirates<\/strong>, utilizing a\u00a0<strong>genomics-enabled clinical development strategy<\/strong>\u00a0designed to optimize patient selection and therapeutic response.<\/p>\n<p align=\"justify\">Key elements of this approach may include:<\/p>\n<ul type=\"disc\">\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">\n          <strong>Hormonal pathway profiling<\/strong>\u00a0to characterize disease biology at the individual patient level<\/li>\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">\n          <strong>Biomarker-driven patient stratification<\/strong>\u00a0to identify patients most likely to benefit<\/li>\n<li style=\"margin-top:5pt;margin-bottom:5pt;text-align:left\">\n          <strong>Precision-informed clinical trial design<\/strong> aimed at improving signal detection and development efficiency<\/li>\n<\/ul>\n<p align=\"justify\">\n        <strong>Notably, no long-acting injectable GnRH antagonists are currently approved for endometriosis, positioning Teverelix as a potential first long-acting injectable therapy in women\u2019s health.\u00a0<\/strong>\n      <\/p>\n<p align=\"justify\">\n        <strong>For further information, contact:<\/strong>\n      <\/p>\n<p align=\"justify\">Carolyn Bonner, President and Chief Financial Officer<br \/>(610) 636-0184<br \/>cbonner@medicuspharma.com\u00a0\u00a0<\/p>\n<p align=\"justify\">Anna Baran-Djokovic, SVP Investor Relations <br \/>(305) 615-9162<br \/>adjokovic@medicuspharma.com\u00a0\u00a0<\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>About Medicus Pharma Ltd.<\/em><br \/>\n        <\/strong>\n      <\/p>\n<p align=\"justify\">\n        <em>Medicus Pharma Ltd. (Nasdaq: MDCX) is a precision-guided biotech\/life sciences company focused on accelerating the clinical development programs of novel and potentially disruptive therapeutics assets. The Company is actively engaged in multiple countries across three continents.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>Company\u2019s key therapeutics assets are:<\/em>\n      <\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>SkinJect\u2122<\/em><br \/>\n        <\/strong><br \/>\n        <strong><br \/>\n          <em>, a novel localized immuno-oncology precision product<\/em><br \/>\n        <\/strong><br \/>\n        <em> focused on non-melanoma skin diseases, especially basal cell carcinoma (BCC) and <\/em><br \/>\n        <strong><br \/>\n          <em>Gorlin Syndrome<\/em><br \/>\n        <\/strong><br \/>\n        <em>, a rare autosomal dominant disease also called nevoid BCC syndrome, collectively representing a ~$2 billion market opportunity.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>Teverelix<\/em><br \/>\n        <\/strong><br \/>\n        <sup><br \/>\n          <strong><br \/>\n            <em>\u00ae<\/em><br \/>\n          <\/strong><br \/>\n        <\/sup><br \/>\n        <strong><br \/>\n          <em>, a next generation GnRH antagonist<\/em><br \/>\n        <\/strong><br \/>\n        <em> is a first-in-market product for cardiovascular high-risk advanced prostate cancer patients and patients with acute urinary retention relapse (AURr) episodes due to enlarged prostate, collectively representing a ~$6 billion market opportunity.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>The Company is actively engaged in following collaborations:<\/em>\n      <\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>Skinject\u2122 Platform Expansion <\/em><br \/>\n        <\/strong>\n      <\/p>\n<p align=\"justify\">\n        <em>In August 2025, the Company announced its entry into a non-binding memorandum of understanding (MoU) with Helix Nanotechnologies, Inc. (HelixNano), a Boston-based biotech company focused on developing a proprietary advanced mRNA platform, in respect of their shared mutual interest in the development or commercial arrangement contemplated by the MoU. The MoU is non-binding and shall not be construed to obligate either party to proceed with a joint venture or any further development or commercial arrangement, unless and until definitive agreements are executed, and there can be no assurance that such definitive agreements will be executed.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>The Company is exploring co-development of thermostable infectious disease vaccines combining HelixNano\u2019s proprietary mRNA technology with the Medicus microneedle array delivery platform.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>Patient Access and Advocacy<\/em><br \/>\n        <\/strong>\n      <\/p>\n<p align=\"justify\">\n        <em>In October 2025, the Company announced <\/em><br \/>\n        <em>a strategic collaboration with the\u00a0Gorlin Syndrome Alliance (GSA)\u00a0to advance compassionate access to\u00a0SkinJect for patients suffering from\u00a0Gorlin Syndrome, also known as nevoid basal cell carcinoma syndrome.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>In collaboration with the Gorlin Syndrome Alliance, Medicus is pursuing an Expanded Access IND program to provide Gorlin Syndrome patients with multiple or inoperable BCCs access to SkinJect\u2122, the Company\u2019s investigational D-MNAs, under physician supervision.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>AI Enabled Clinical Development<\/em><br \/>\n        <\/strong>\n      <\/p>\n<p align=\"justify\">\n        <em>In December 2025, the Company signed a non-binding letter of intent to collaborate with Reliant AI Inc., a decision-intelligence company specializing in generative AI for the life sciences, to develop an AI-driven clinical data analytics platform to support capital-efficient and time-efficient clinical development through data-driven dynamic clinical-site selection, pharmacodynamic (PD) informed patient stratification, and enrollment forecasting. The initial phase of the collaboration is expected to support the upcoming Teverelix clinical study planned for 2026. There can be no assurance that a definitive agreement will be executed or that the proposed collaboration will proceed as contemplated.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>Cautionary Notice on Forward-Looking Statements<\/em><br \/>\n        <\/strong>\n      <\/p>\n<p align=\"justify\">\n        <em>Certain information in this news release constitutes &#8220;forward-looking information&#8221; under applicable securities laws. &#8220;Forward-looking information&#8221; is defined as disclosure regarding possible events, conditions or financial performance that is based on assumptions about future economic conditions and courses of action and includes, without limitation, statements regarding the Company\u2019s ability to continue as a going concern, statements regarding the Company\u2019s leadership and prospects, the collaboration with GSA including the potential benefits thereof for GSA, those suffering with Gorlin Syndrome and Medicus (including as it relates to the development of SkinJect\u2122), ability to be approved for the Expanded Access IND Program to enable those suffering with Gorlin Syndrome to access SkinJect\u2122 under physician-supervised treatment protocols, the development of Teverelix and expectations concerning, and future outcomes relating to, the development, advancement and commercialization of Teverelix for AURr, high CV risk prostate cancer, women\u2019s health indications like endometriosis, and the potential market opportunities related thereto, the MOU, including the potential signing of definitive agreements between Medicus and HelixNano and the development of thermostable infectious diseases vaccines by combining HelixNano\u2019s proprietary mRNA vaccine platform with Medicus\u2019s proprietary microneedle array (MNA) delivery platform, the Company\u2019s aim to fast-track the clinical development program and convert the SKNJCT-003 exploratory clinical trial into a pivotal clinical trial, and approval from the FDA and the timing thereof, including with respect to the Company\u2019s submission for approval in the FDA <\/em><br \/>\n        <em>Commissioner&#8217;s National Priority Voucher program<\/em><br \/>\n        <em>, plans and expectations concerning, and future outcomes relating to, the development, advancement and commercialization of SkinJect through SKNJCT-003 and SKNJCT-004, and the potential market opportunities related thereto, the Company\u2019s expectations regarding reported efficacy findings, the overall response rate and potential changes thereto, and whether there will be material changes to its reported SKNJCT-003 topline results and to secure an EOP2 meeting with the FDA in the first half of 2026, entry into definitive documents with Reliant and the expected terms thereof, engaging in proposed Medicus-sponsored studies currently contemplated in the Reliant non-binding letter of intent and the expected benefits thereof, the expansion of SKNJCT-003 into the United Kingdom and the potential benefits therefrom, the advancement of the SKNJCT-004 study and the potential results of and benefits of such study. Forward-looking statements are often but not always, identified by the use of such terms as &#8220;may&#8221;, \u201con track\u201d, \u201caim\u201d, &#8220;might&#8221;, &#8220;will&#8221;, &#8220;will likely result&#8221;, \u201ccould,\u201d \u201cdesigned,\u201d &#8220;would&#8221;, &#8220;should&#8221;, &#8220;estimate&#8221;, &#8220;plan&#8221;, &#8220;project&#8221;, &#8220;forecast&#8221;, &#8220;intend&#8221;, &#8220;expect&#8221;, &#8220;anticipate&#8221;, &#8220;believe&#8221;, &#8220;seek&#8221;, &#8220;continue&#8221;, &#8220;target&#8221;, \u201cpotential\u201d or the negative and\/or inverse of such terms or other similar expressions. These statements involve known and unknown risks, uncertainties and other factors, which may cause actual results, performance or achievements to differ materially from those expressed or implied by such statements, including those risk factors described in the Company&#8217;s annual report on form 10-K for the year ended December 31, 2025, and in the Company&#8217;s other public filings on EDGAR and SEDAR+, which may impact, among other things, the trading price and liquidity of the Company&#8217;s common shares. Forward-looking statements contained in this news release are expressly qualified by this cautionary statement and reflect our expectations as of the date hereof and thus are subject to change thereafter. The Company disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. Readers are further cautioned not to place undue reliance on forward-looking statements as there can be no assurance that the plans, intentions or expectations upon which they are placed will occur. Such information, although considered reasonable by management at the time of preparation, may prove to be incorrect and actual results may differ materially from those anticipated.<\/em>\n      <\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTY4ODgzOSM3NTMyODcyIzIzMDUxNzk=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/YzEwYzNkY2MtNmU3MC00MDI5LTk4NzAtZTA3YzY5MDU3ODVmLTEzMTY3MjktMjAyNi0wNC0xNS1lbg==\/tiny\/Medicus-Pharma-Ltd.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Updated Safety, Efficacy, and Clinical Data Supports Teverelix as Potentially the First Long-Acting Injectable GnRH Antagonist Across Multiple Indications in Women\u2019s Health PHILADELPHIA, April 15, 2026 (GLOBE NEWSWIRE) &#8212; Medicus Pharma Ltd. (NASDAQ: MDCX) (&#8220;Medicus&#8221; or the &#8220;Company&#8221;), a biotech\/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced it will present new Phase 1 clinical data on Teverelix, its investigational long-acting gonadotropin-releasing hormone (GnRH) antagonist, at the\u00a0American Association of Clinical Endocrinology Annual Meeting 2026 (AACE 2026) on April 22-24th in Las Vegas, Nevada. Teverelix is being developed for hormone-driven conditions, with potential applications in women\u2019s health, including endometriosis and uterine fibroids. Faisal Mehmud, MD, MRCP, the Company\u2019s Chief Medical Officer, &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression&#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-951542","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression - 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\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Updated Safety, Efficacy, and Clinical Data Supports Teverelix as Potentially the First Long-Acting Injectable GnRH Antagonist Across Multiple Indications in Women\u2019s Health PHILADELPHIA, April 15, 2026 (GLOBE NEWSWIRE) &#8212; Medicus Pharma Ltd. (NASDAQ: MDCX) (&#8220;Medicus&#8221; or the &#8220;Company&#8221;), a biotech\/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced it will present new Phase 1 clinical data on Teverelix, its investigational long-acting gonadotropin-releasing hormone (GnRH) antagonist, at the\u00a0American Association of Clinical Endocrinology Annual Meeting 2026 (AACE 2026) on April 22-24th in Las Vegas, Nevada. Teverelix is being developed for hormone-driven conditions, with potential applications in women\u2019s health, including endometriosis and uterine fibroids. Faisal Mehmud, MD, MRCP, the Company\u2019s Chief Medical Officer, &hellip; Continue reading &quot;Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-04-15T12:21:56+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTY4ODgzOSM3NTMyODcyIzIzMDUxNzk=\" \/>\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=\"8 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\\\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression\",\"datePublished\":\"2026-04-15T12:21:56+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\\\/\"},\"wordCount\":1572,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTY4ODgzOSM3NTMyODcyIzIzMDUxNzk=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\\\/\",\"name\":\"Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression - 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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\/medicus-pharma-to-present-new-teverelix-data-at-aace-2026-demonstrating-long-acting-hormone-suppression\/","og_locale":"en_US","og_type":"article","og_title":"Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression - Market Newsdesk","og_description":"Updated Safety, Efficacy, and Clinical Data Supports Teverelix as Potentially the First Long-Acting Injectable GnRH Antagonist Across Multiple Indications in Women\u2019s Health PHILADELPHIA, April 15, 2026 (GLOBE NEWSWIRE) &#8212; Medicus Pharma Ltd. (NASDAQ: MDCX) (&#8220;Medicus&#8221; or the &#8220;Company&#8221;), a biotech\/life sciences company focused on advancing the clinical development programs of novel and potentially disruptive therapeutics assets, today announced it will present new Phase 1 clinical data on Teverelix, its investigational long-acting gonadotropin-releasing hormone (GnRH) antagonist, at the\u00a0American Association of Clinical Endocrinology Annual Meeting 2026 (AACE 2026) on April 22-24th in Las Vegas, Nevada. Teverelix is being developed for hormone-driven conditions, with potential applications in women\u2019s health, including endometriosis and uterine fibroids. 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