{"id":992656,"date":"2026-08-10T08:05:58","date_gmt":"2026-08-10T12:05:58","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\/"},"modified":"2026-08-10T08:05:58","modified_gmt":"2026-08-10T12:05:58","slug":"elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\/","title":{"rendered":"Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma"},"content":{"rendered":"<div class=\"mw_release\">\n<ul type=\"disc\">\n<li style=\"margin-top:6pt;margin-bottom:6pt\">Phase 1 study conducted by Memorial Sloan Kettering (\u201cMSK\u201d) Cancer Center and funded by The Lustgarten Foundation<\/li>\n<li style=\"margin-top:6pt;margin-bottom:6pt\">Study to evaluate ELI-002 7P in combination with chemotherapy and checkpoint inhibition in the neoadjuvant setting<\/li>\n<li style=\"margin-top:6pt;margin-bottom:6pt\">Expected to enroll 20 patients with resectable or borderline resectable pancreatic ductal adenocarcinoma (\u201cPDAC\u201d)\n<\/li>\n<\/ul>\n<p>BOSTON, Aug.  10, 2026  (GLOBE NEWSWIRE) &#8212; Elicio Therapeutics, Inc. (Nasdaq: ELTX) (\u201cElicio\u201d or the \u201cCompany\u201d), a clinical-stage biotechnology company developing next-generation immunotherapies for KRAS-driven cancers, today announced the opening of the investigator-initiated (\u201cIIT\u201d) Phase 1 neoadjuvant study (<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=qZhnF-p01DrkRTNLf3EzMqjPfowgnSVWJSIrP1IjRGXK3WEcEKw76U19YWr1Rmua5ORbn7fsLyFNDAvaz4wV-0Zksya7G2-tElh06OUw2K6FiwWKxtpqboK4uuRlJKD9sPDZ3v-Q4TYWZ_SIkUXSd0qPOUL6T7nCBEmEWyH5wFMGt2Za57549cqqXrh6NyP3osqRgbgm6BU2GOQPE_jsRp9rSdJKZFcjweByZSj6J9XgIhx_z4wZwY5O_AyVvMlA4rUPRInNIuD_h3_JMY31qw==\" rel=\"nofollow\" target=\"_blank\">NCT07671339<\/a>) evaluating ELI-002 7P in combination with chemotherapy and an anti-PD1 checkpoint inhibitor in borderline resectable and resectable PDAC. The multi-center IIT is being conducted by MSK Cancer Center and is being funded by a strategic partnership between The Lustgarten Foundation and Break <em>Through<\/em> Cancer.<\/p>\n<p>\u201cThe activation of this study marks an important milestone as we prepare to evaluate the potential of ELI-002 7P across multiple stages of pancreatic cancer,\u201d said Christopher Haqq, M.D., Ph.D., Executive Vice President, Head of Research and Development and Chief Medical Officer of Elicio. \u201cBuilding on the complete responses observed in patients with metastatic PDAC treated with sequential ELI-002 7P followed by checkpoint inhibitor and chemotherapy, this study prospectively evaluates the combination beginning in the neoadjuvant setting and continuing after surgery. We hope to generate important clinical insights into ELI-002 7P\u2019s potential to harness the immune system and improve surgical outcomes and long-term survival for patients facing this devastating disease.\u201d<\/p>\n<p>Kevin Soares, MD, Assistant Attending Surgeon Hepatopancreatobiliary Service, MSK and Principal Investigator of the Phase 1 study added, \u201cDespite advances in the treatment of pancreatic cancer, patients with resectable and borderline resectable disease continue to face a high risk of recurrence, highlighting the need for new therapeutic strategies. This trial offers an important opportunity to investigate how ELI-002 7P may reshape the tumor immune environment when initially combined with neoadjuvant therapy, while offering the potential to generate valuable translational data that could inform future treatment strategies.\u201d<\/p>\n<p>The randomized, open-label Phase 1 trial aims to enroll 20 patients with resectable or borderline resectable KRAS-mutant PDAC. Participants will receive ELI-002 7P with standard chemotherapy, mFOLFIRINOX, with or without tislelizumab, an anti-PD1 checkpoint inhibitor, starting before surgery. Throughout treatment, researchers plan to collect tumor tissue and blood samples to better understand immune activation, characterize changes within the tumor microenvironment, and identify biomarkers that could guide future clinical trials.<\/p>\n<p>\n        <strong>About ELI-002<\/strong>\n      <\/p>\n<p>Elicio\u2019s lead product candidate, ELI-002, is a structurally novel investigational AMP cancer immunotherapy that targets cancers that are driven by mutations in the KRAS-gene\u2014a prevalent driver of many human cancers. ELI-002 is comprised of two powerful components that are built with Elicio\u2019s proprietary AMP technology consisting of AMP-modified mutant KRAS peptide antigens and ELI-004, an AMP-modified CpG oligodeoxynucleotide adjuvant that is available as an off-the-shelf subcutaneous administration.<\/p>\n<p>ELI-002 7P (7-peptide formulation) was evaluated in the randomized Phase 2 AMPLIFY-7P trial in patients with mKRAS-driven pancreatic cancer (NCT05726864). The Phase 2 AMPLIFY-7P trial included patients with mKRAS-positive pancreatic cancer who completed standard therapy but remain at high risk of relapse. Elicio continues to evaluate pre-specified subgroups, including the R0 resected population, to further inform a refined Phase 3 development strategy. Elicio intends to initiate a Phase 1 study in metastatic PDAC designed to provide a rapid assessment of clinical activity using an open label design to assess the objective response rate including partial and complete radiographic responses. Elicio plans to use the study findings to further evaluate checkpoint inhibitor combinations and help inform future development strategies in metastatic PDAC and the adjuvant PDAC Phase 3 trial. At the time of the Phase 2 AMPLIFY-7P analysis, data for overall survival remained immature. The ELI-002 7P formulation is designed to provide immune response coverage against seven of the most common KRAS mutations present in 25% of all solid tumors, thereby increasing the potential patient population for ELI-002.<\/p>\n<p>\n        <strong>About Elicio Therapeutics <\/strong>\n      <\/p>\n<p>Elicio Therapeutics, Inc. (Nasdaq: ELTX) is a clinical-stage biotechnology company advancing novel immunotherapies for the treatment of high-prevalence cancers, including mKRAS-positive pancreatic and colorectal cancers. Elicio intends to build on recent clinical findings in the personalized cancer immunotherapy space to develop effective, off-the-shelf immunotherapies. Elicio\u2019s AMP technology aims to enhance the education, activation and amplification of cancer-specific T cells relative to conventional immunotherapy strategies, with the goal of promoting durable cancer immunosurveillance in patients. Elicio\u2019s ELI-002 7P lead program is an off-the-shelf immunotherapy candidate targeting the most common KRAS mutations, which drive approximately 25% of all solid tumors. Off-the-shelf immunotherapy approaches have the potential benefits of low cost, rapid commercial scale manufacturing, and rapid availability of drug to patients, especially in neo-adjuvant settings and for prophylaxis in high-risk patients, contrary to personalized immunotherapy approaches. ELI-002 7P was evaluated in the randomized Phase 2 AMPLIFY-7P trial in patients with mKRAS-positive pancreatic cancer who completed standard therapy but remain at high risk of relapse. Elicio continues to evaluate pre-specified subgroups, including the R0 resected population, to further inform a refined Phase 3 development strategy. Elicio intends to initiate a Phase 1 study in metastatic PDAC designed to provide a rapid assessment of clinical activity using an open label design to assess the objective response rate including partial and complete radiographic responses. Elicio plans to use the study findings to further evaluate checkpoint inhibitor combinations and help inform future development strategies in metastatic PDAC and the adjuvant PDAC Phase 3 trial. ELI-002 also has been studied in patients with mKRAS-positive colorectal cancer in Phase 1 studies. In the future, Elicio plans to expand ELI-002 7P to other indications, including mKRAS positive lung cancer and other mKRAS positive cancers. Elicio\u2019s pipeline includes additional off-the-shelf therapeutic cancer immunotherapy candidates, including ELI-007 and ELI-008, that target BRAF-driven cancers and p53 hotspot mutations, respectively.<\/p>\n<p>\n        <strong>About Break <\/strong><br \/>\n        <strong><br \/>\n          <em>Through <\/em><br \/>\n        <\/strong><br \/>\n        <strong>Cancer<\/strong>\n      <\/p>\n<p>Founded in 2021, Break <em>Through <\/em>Cancer empowers outstanding researchers and physicians to both intercept and find cures for several of the deadliest cancers by stimulating radical collaboration among outstanding cancer research institutions, including its founding partners: Dana-Farber Cancer Institute, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Memorial Sloan Kettering Cancer Center, MIT\u2019s Koch Institute for Integrative Cancer Research, and The University of Texas MD Anderson Cancer Center.<\/p>\n<p>The Foundation is supported by a Board of Directors from the five partner institutions and a Scientific Advisory Board of U.S. cancer experts. The Foundation was launched with an extraordinary challenge pledge of $250 million from Mr. and Mrs. William H. Goodwin, Jr. and their family, and the estate of William Hunter Goodwin III.<\/p>\n<p>For further information, please visit the Foundation\u2019s website at <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=H41OQy0FUBLKyN0ob-yGgC6TReGz-rPdu12jvOH9jHaawKw9lzy-slnPxJ-3a-_-BxLJofwDG7n3XjV5ApzM3H4eQY0lDMaseZhYizToMaO2E_zmUXZJzlJnucf6aWgfeGUyhYWrEnXkxQTFvmqh3xFcIgnJ0blIp4Wmj0cVz7FOUZCt8ZOjlUqcilXC6SMeIyIoULhraaneYf-eKvKnn4Vkr6HOgrRdArqiVeeuCF9rZsFy17Us-WjNYAQ7-90UAsDdYxe2JG8H3ND0NsP6QvXCkgAXxxfMTQs_E7P3zh2EnUAbL4Y3jlYZVg92muO0NMHlCA391w5oPB5nrqesfxrxF9-rNYE6xLYQJw4V4QaIlQV1qmF_ehcsCXqYxzCHpXio-eG-5KdfLTtdLQBTVw==\" rel=\"nofollow\" target=\"_blank\">www.breakthroughcancer.org<\/a>.<\/p>\n<p>\n        <strong>About The Lustgarten Foundation<\/strong>\n      <\/p>\n<p>The Lustgarten Foundation is the largest private funder of pancreatic cancer research in the world, funding preeminent pancreatic cancer research, driving the pursuit of bold and innovative science toward earlier detection and better treatments, and transforming pancreatic cancer into a curable disease. The Foundation funds research where creative risks yield high rewards to accelerate and expand life-saving treatment options. The Lustgarten foundation believes time is everything to patients and their families, and that community is power. Lustgarten programs and events provide people affected by pancreatic cancer a voice and a place to create hope, together.<\/p>\n<p>For more information about the Lustgarten Foundation, visit\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=degwbznOL7UpPn2oI3bDogSdSzEn8bxq-7tZVgQnOdMXethji7yE-RYNfeVcvMKnhF9d-YWwkK8i8o2XG0Owc30B24gXgyeMB5vmG0QjdtGwNeG44Q8C1xQMHUqjcxOBygE_OScutLF78wJAlBlci2UVLe8y4W0mJSkJcq3jgM9UXvXc9vZQfkdj6oOaDfyAXuZxw3wjSeGG59A2eOmIFLvFFTr-yBcJZcw7Z1svNKg=\" rel=\"nofollow\" target=\"_blank\"><strong>lustgarten.org<\/strong><\/a><a 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rel=\"nofollow\" target=\"_blank\"><strong>.<\/strong><\/a><\/p>\n<p>\n        <strong>Elicio Cautionary Note on Forward-Looking Statements<\/strong>\n      <\/p>\n<p>Certain statements contained in this communication regarding matters that are not historical facts, are forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995, known as the PSLRA. These include statements regarding Elicio\u2019s planned clinical programs, including the IIT; the timing, enrollment, and outcome of Elicio\u2019s planned clinical trials; the potential of Elicio\u2019s product candidates and platform; the potential to generate important clinical insights into ELI-002 7P\u2019s potential to harness the immune system and improve surgical outcomes and long-term survival for patients with PDAC; the potential benefits of combining standard neoadjuvant chemotherapy with immunotherapies, including the combination of mFOLFIRINOX with ELI-002 7P, with or without tislelizumab; the potential for ELI-002 7P to reshape the tumor immune environment when combined with neoadjuvant therapy; the potential for the IIT to generate valuable translational data to inform future treatment strategies; the potential for future expansion of ELI-002 to other indications, including mKRAS positive lung cancer and other mKRAS positive cancers; the potential benefits and effectiveness of off-the-shelf vaccine approaches; and other statements regarding management\u2019s intentions, plans, beliefs, expectations or forecasts for the future and, therefore, you are cautioned not to place undue reliance on them. No forward-looking statement can be guaranteed, and actual results may differ materially from those projected. Elicio undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise, except to the extent required by law. We use words such as \u201canticipates,\u201d \u201cbelieves,\u201d \u201cplans,\u201d \u201cexpects,\u201d \u201cprojects,\u201d \u201cfuture,\u201d \u201cintends,\u201d \u201cmay,\u201d \u201cwill,\u201d \u201cshould,\u201d \u201ccould,\u201d \u201cestimates,\u201d \u201cpredicts,\u201d \u201cpotential,\u201d \u201ccontinue,\u201d \u201cguidance,\u201d and similar expressions to identify these forward-looking statements that are intended to be covered by the safe-harbor provisions of the PSLRA. Such forward-looking statements are based on Elicio\u2019s expectations and involve risks and uncertainties; consequently, actual results may differ materially from those expressed or implied in the statements due to a number of factors, including, but not limited to, Elicio\u2019s plans to develop and commercialize its product candidates, including ELI-002; the timing of the availability of data from Elicio\u2019s clinical trials; the timing of any planned investigational new drug application or new drug application; Elicio\u2019s plans to research, develop and commercialize its current and future product candidates; and Elicio\u2019s estimates regarding future revenue, expenses, capital requirements and need for additional financing.<\/p>\n<p>New factors emerge from time to time, and it is not possible for Elicio to predict all such factors, nor can Elicio assess the impact of each such factor on the business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. These risks are more fully discussed under the heading \u201cRisk Factors\u201d in Elicio\u2019s Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on March 12, 2026, as amended on April 29, 2026, its Quarterly Report on Form 10-Q for the quarter ended March 31, 2026, filed with the SEC on May 11, 2026, and any subsequent reports and other documents filed from time to time with the SEC. Forward-looking statements included in this release are based on information available to Elicio as of the date of this release. Elicio does not undertake any obligation to update such forward-looking statements to reflect events or circumstances after the date of this release, except to the extent required by law.<\/p>\n<p>\n        <strong>Elicio Investor Relations Contact<\/strong>\n      <\/p>\n<p>Brian Ritchie<br \/>LifeSci Advisors<br \/>(212) 915-2578<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=8rwxuCwmmmNxf3qmhxcBjGZ6hI3g6Hc-Keu6tA-IzXETTDnLUM7xD-Wz2SWdKTjqo3rNYCnj3f9UZE6j_H9W6Jkr4l-jYXPYx-9f4XRFhZonlDeI791TKv4vNjQpqmuf\" rel=\"nofollow\" target=\"_blank\">britchie@lifesciadvisors.com<\/a><\/p>\n<p>\n        <strong>Elicio Media Contact<\/strong>\n      <\/p>\n<p>Michael Fitzhugh<br \/>LifeSci Communications<br \/>(415) 269-7757<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=KfS344iZG-rnHHOb4b4I7uAXoqGnXmXtPTmi1X8er155T7kT37nRY5EMDxMhEzn4PA92kfQDirIrqCV26ORwYpA8oZWqH77OjRapbnoN0plhmYqoiz0GhDBBiZDiJKzr\" rel=\"nofollow\" target=\"_blank\">mfitzhugh@lifescicomms.com<\/a><\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTgwNjI4OSM3NzY2MDM0IzIyMDg2Nzk=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/M2I3Y2FmYjYtZGJlMS00NGU3LWJlODMtYzEyYTY1MmMwM2FkLTEyMjAyMzItMjAyNi0wOC0xMC1lbg==\/tiny\/Elicio-Therapeutics-Inc-.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Phase 1 study conducted by Memorial Sloan Kettering (\u201cMSK\u201d) Cancer Center and funded by The Lustgarten Foundation Study to evaluate ELI-002 7P in combination with chemotherapy and checkpoint inhibition in the neoadjuvant setting Expected to enroll 20 patients with resectable or borderline resectable pancreatic ductal adenocarcinoma (\u201cPDAC\u201d) BOSTON, Aug. 10, 2026 (GLOBE NEWSWIRE) &#8212; Elicio Therapeutics, Inc. (Nasdaq: ELTX) (\u201cElicio\u201d or the \u201cCompany\u201d), a clinical-stage biotechnology company developing next-generation immunotherapies for KRAS-driven cancers, today announced the opening of the investigator-initiated (\u201cIIT\u201d) Phase 1 neoadjuvant study (NCT07671339) evaluating ELI-002 7P in combination with chemotherapy and an anti-PD1 checkpoint inhibitor in borderline resectable and resectable PDAC. The multi-center IIT is being conducted by MSK Cancer Center and is being funded by a &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma&#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-992656","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma - 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\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Phase 1 study conducted by Memorial Sloan Kettering (\u201cMSK\u201d) Cancer Center and funded by The Lustgarten Foundation Study to evaluate ELI-002 7P in combination with chemotherapy and checkpoint inhibition in the neoadjuvant setting Expected to enroll 20 patients with resectable or borderline resectable pancreatic ductal adenocarcinoma (\u201cPDAC\u201d) BOSTON, Aug. 10, 2026 (GLOBE NEWSWIRE) &#8212; Elicio Therapeutics, Inc. (Nasdaq: ELTX) (\u201cElicio\u201d or the \u201cCompany\u201d), a clinical-stage biotechnology company developing next-generation immunotherapies for KRAS-driven cancers, today announced the opening of the investigator-initiated (\u201cIIT\u201d) Phase 1 neoadjuvant study (NCT07671339) evaluating ELI-002 7P in combination with chemotherapy and an anti-PD1 checkpoint inhibitor in borderline resectable and resectable PDAC. The multi-center IIT is being conducted by MSK Cancer Center and is being funded by a &hellip; Continue reading &quot;Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-08-10T12:05:58+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTgwNjI4OSM3NzY2MDM0IzIyMDg2Nzk=\" \/>\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=\"9 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\\\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma\",\"datePublished\":\"2026-08-10T12:05:58+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\\\/\"},\"wordCount\":1818,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTgwNjI4OSM3NzY2MDM0IzIyMDg2Nzk=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/elicio-therapeutics-announces-activation-of-the-investigator-initiated-phase-1-study-of-neoadjuvant-eli-002-7p-for-pancreatic-ductal-adenocarcinoma\\\/\",\"name\":\"Elicio Therapeutics Announces Activation of the Investigator-Initiated Phase 1 Study of Neoadjuvant ELI-002 7P for Pancreatic Ductal Adenocarcinoma - 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(Nasdaq: ELTX) (\u201cElicio\u201d or the \u201cCompany\u201d), a clinical-stage biotechnology company developing next-generation immunotherapies for KRAS-driven cancers, today announced the opening of the investigator-initiated (\u201cIIT\u201d) Phase 1 neoadjuvant study (NCT07671339) evaluating ELI-002 7P in combination with chemotherapy and an anti-PD1 checkpoint inhibitor in borderline resectable and resectable PDAC. 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