{"id":770910,"date":"2023-07-19T10:26:12","date_gmt":"2023-07-19T14:26:12","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/"},"modified":"2023-07-19T10:26:12","modified_gmt":"2023-07-19T14:26:12","slug":"panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/","title":{"rendered":"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds"},"content":{"rendered":"<div class=\"mw_release\">\n<p align=\"left\">\n        <strong>MINNEAPOLIS and LOUISVILLE, Ky., July  19, 2023  (GLOBE NEWSWIRE) &#8212; Panbela Therapeutics, Inc. <\/strong>(Nasdaq: PBLA), a clinical stage company developing disruptive therapeutics for the treatment of patients with urgent unmet medical needs, today announced it has divested certain assets in its eflornithine pediatric neuroblastoma program to<strong> US <\/strong><strong>WorldMeds<\/strong><strong>\u00ae<\/strong><sup><strong>1<\/strong><\/sup> (USWM), a Kentucky-based specialty pharmaceutical company.<\/p>\n<p>Neuroblastoma, a rare cancer originating from immature nerve cells, contributes to nearly 15% of pediatric cancer deaths.<sup>[1]<\/sup> Panbela Therapeutics&#8217; subsidiary, Cancer Prevention Pharmaceuticals, has extensively collaborated with leading neuroblastoma research groups such as the Neuroblastoma Medulloblastoma Translational Research Consortium (NMTRC) (now Beat Childhood Cancer), New Advances in Neuroblastoma Therapy (NANT), the Children\u2019s Oncology Group (COG), and the National Cancer Institute (NCI) in the clinical development of eflornithine as a treatment for neuroblastoma. These collaborative efforts, spanning multiple years, have resulted in the Company receiving orphan drug designations for the use of eflornithine in the treatment of neuroblastoma in both the United States and Europe.<\/p>\n<p>Under the terms of the agreement, Panbela is entitled to receive up to approximately $9.5 million non-dilutive funding in exchange for the sale of certain assets within its pediatric neuroblastoma program for eflornithine. Panbela will receive payments upon USWM\u2019s successful completion of milestones related to eflornithine&#8217;s clinical development, regulatory approval, and commercial sales.<\/p>\n<p>\u201cDivesting eflornithine assets for pediatric neuroblastoma is another milestone in executing our business plan to generate long-term value for our shareholders. US WorldMeds\u2019 existing focus in neuroblastoma makes them an ideal company to further its clinical development in that indication,\u201d said Jennifer K. Simpson, PhD, MSN, CRNP, President &amp; Chief Executive Officer of Panbela. \u201cThis agreement further expands our portfolio of partner-funded programs and has the potential to generate considerable development milestone payments. We welcome US WorldMeds to our portfolio of partners who continue the development of our product candidates.\u201d<\/p>\n<p>\u201cWe are excited that the agreement will help address this high unmet need through the further development of eflornithine for the treatment of patients with neuroblastoma,\u201d said Elizabeth Bruckheimer, Ph.D., Vice President &amp; Chief Scientific Officer of Panbela. \u201cAfter investigating the role of polyamines and the therapeutic potential of eflornithine in neuroblastoma for many years, it is comforting to be passing the baton to the capable hands at USWM. We look forward to helping USWM with the ongoing FDA review of their New Drug Application for eflornithine and future research efforts for patients with neuroblastoma.\u201d<\/p>\n<p>&#8220;This transaction strengthens and expands our neuroblastoma program data currently under FDA review and builds upon our established partnerships to fully unleash the potential of DFMO as a breakthrough treatment for neuroblastoma,&#8221; commented Paul Breckinridge Jones, Chief Executive Officer of US WorldMeds. &#8220;Our agreement with Panbela supports our overarching objective of redefining the standard of care and significantly improving outcomes for children with this devastating disease, who are in urgent need of new therapies.&#8221;<\/p>\n<p>\n        <strong>About our Pipeline<\/strong>\n      <\/p>\n<p>The pipeline consists of assets currently in clinical trials with an initial focus on familial adenomatous polyposis (FAP), first-line metastatic pancreatic cancer, neoadjuvant pancreatic cancer, colorectal cancer prevention and ovarian cancer. The combined development programs have a steady cadence of catalysts with programs ranging from pre-clinical to registration studies.<\/p>\n<p>\n        <strong>SBP-101\u00a0Ivospemin<\/strong>\n      <\/p>\n<p>Ivospemin is a proprietary polyamine analogue designed to induce polyamine metabolic inhibition (PMI) by exploiting an observed high affinity of the compound for pancreatic ductal adenocarcinoma and other tumors. It has shown signals of tumor growth inhibition in clinical studies of metastatic pancreatic cancer patients, demonstrating a median overall survival (OS) of 14.6 months and an objective response rate (ORR) of 48%, both exceeding what is typical for the standard of care of gemcitabine + nab-paclitaxel suggesting potential complementary activity with the existing FDA-approved standard chemotherapy regimen. In data evaluated from clinical studies to date, ivospemin has not shown exacerbation of bone marrow suppression and peripheral neuropathy, which can be chemotherapy-related adverse events. Serious visual adverse events have been evaluated and patients with a history of retinopathy or at risk of retinal detachment will be excluded from future SBP-101 studies. The safety data and PMI profile observed in the previous Panbela-sponsored clinical trials provide support for continued evaluation of ivospemin in the ASPIRE trial. For more information, please visit\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=0FeDONdABawxZb33Yb1dZeywbkVZxkwUF08nB0V_qxWqSjxPm4DH8Mk6np_Luy-zZMnGufaPJFkarYWxiXZ6R84g1qt9R51QYAq6iVgaSHTtkAxO5tWQxAWsqaLwYPXIjP2McUmmXR0TmJSTCustSHt9a0Xn5F_BWeVv7FN3K9GrvtF-Cg392zgzYi8ly5hbJu-rCITxF2SCiNvu8Ea-GBnLHiDAUJo8XNHKTx-KZrTpTaoSS17K7-Bl4eGb0Rpzj4rXjiDnsEKISSS2Wu51C1UBpv8f5vwbdQS8HJG-A568Vcv1ZFTH6dgJF6mVBnQMfbTRDaDHfThYlPFc9s8jS9veXDOrGPZA0kDSU3q5Cc0lKSiUIcSWIXdVTcI1x-qQ8wkQ6zQ85Qi69Ola1B891W4r8dstwb5ltwr1p75yIW-vymj0EKIbgBnYfC2FA2ywITTw1KBogAFOK5iTdwrjMZqWWcuQ-zCX7rqA731EFN53ZfnVdXryruO9JhJtz63s5UDBvemAsVdGy6fT-02b3NzlgEf1AmpZzrGoOHIRT8j_hym_9-1kl2O1dSq1XeU8CI0ookfTbeMu4L_iYt_Azw2GxXGuvHjBMXsl5AADgjncBLuSWbouFYrcsTqFrMtHh6Zi-4TnR6GHPfPaCX7NowR3Yu0-idEG01bEholdRO6wqQAffkForoi9EUqtsWzIu6N3SOlI4hvZo5Y1GFf_N6N8exewXo3FtqcKgD3NWKwJvtHgPzeNufXjjJj0Z4cgqUvlCwbm_gAYSTKNuYSMuSUr36evMahHi3-69q7SFFfAhtSVltlcKaU72PlWYs2jwuLL7hkWfTjDCBcFv7vRPmhiPBbWM4pMIjePT3v4j8NRzP5ae0GI4ehViTk29hRF6aeFTqoxmQ55JXUe3QnToHblz3edRCWKyfonoxfbYNV8IxRMc0377oIlqxFdKDU636uakXf4wmsoe6maJ_wP9Ic9HHhbSvZD0STns_CzG0YiyUGKs6aC7-qq8S72BKlXtNvvoCCn-nikVUtCQ6aKq3xPLxH8-kPzYZ8Yyy4KssQkFpDtUWppt4Klqb9y4qdBbQ5eZ1j7gw0xgZCz3Xhm__jWhjpUxp7_dyHIO3SAqYxufBwHUZ1z1XN5kXMrEjdCC9aDQd_H78Wwt7_v-_u6TJ0kWPiLmdque5IJrch8YvcA7Z8ViO-UIh2Rw8qe0NoOUHaJLglR7UVnFl6DXuPiZmGqnPng8ruzWYepinrWT37bMphjjGtSFJnmYB6fojTG-CJoHrq-8S1BsFXJsNeOYWxkk56HOvdZGnWTkSCMbM__00wABRXy-8zaQHtFrHdltav6j1B1u9RaU8bzsOHHyjzgRuOFzBmj21GuguJsooQ_XOFHlIrqhnTPeyKHL-59VXFJrOnB_EP89vCACJjS7HzmnlmysFv4q0NsctvM8y--IDUPnSKxbmTNwmYTZQlRZVGJG_4ts2aoYf_tRktVcCyALYElO-0WKcYISzv66XAZJod_bgI5rvw9fw1-nNOiJUTdPcbtPGQae2RkXnsvnQhHnS8l6hpKdTKf-F6ndZfuOm7Mogx92IEtF4XjneI9DkM2DcfaQf4gvn6fKP_KuvwLFE-ww3W1uCeUrNffFH0BO73edhPlZ5jEuFWziuUlujbFpCX9ahjgfkIQw9D3xjJKdrBcMg7beApt1kPcWC6lLmKXrv8Ou94n-EAd3QicSWL6uuEQpBfRT-_PFORZtFzxp-QKVUFlQIUh5bjJsYiup2Hpgxt4TCGmI5w_j7ALoDTIt71hiTpO6JmCBzPUlthKwj3Mc804nS8ZfM4LDWhpLaeNODqHdEKCgD7vcLJdceCGW9Z6G5EZ_9MeD4n3t7UVTNtb1SxD6gJLfQrKzd-kMGuDy41-EZ6SF44zPebL7-jb17bmfSNJ_VB7rcPU7uAffrzu2pJpek4U-FSIUa6jemyKQpHY9Cyd9-0wg6PZBCmv9KPSHysH7TphAo0UrG-NxxeXYK5nIj5Ucd4EClEprd6tLjVf_ROoXSe8a_KpdlfxxuO-hegbnsGYSoJdTdD__ksUEdTe1RdT8R2vpUB3s7NejSBFqiANnuFB9PSN_yGtBfHbVV6F98QkDXnmJB98Elkdl1o0RJDzhwfmx7plbkBQ6dWFLB3_v5xBbXBslei74qUbBbqKfMMZkGdhgmvgMPoJ-4JXgiSsTLNofg2vQdEY_g22r6oYh0wkTJ8u8OUSTCWvT5qTVgxgpgH4dHoEDWBORqvi7ev408CbAroyB4kozwLR1Okr5fGyHSUmkZdnB8TOSuEKrEkZpskyIxj5Y0fZX1X1T9T3dve0KJoghcJM_U0ZDwTXbcNNK375eagov7gYaGrYNAw9STpI-KOSH5COvsVbP_5r9g0rRWt2EYrVmLAhHlxulg8wlNI6fHyx5QThxQLZ83GJAl3EzxLISJGxCUwielAWXv5GFKOTibf_S6q3lMenpFthkpblv74WwKHJJNUCk6DAh7loBkvrUbpqGYhfKgIQMyX6v_w0ey3ZuFvEbPUTwL0hIW01j3BBPshf4DQSr4bAdgIB2njH5GhfJX-Pz17ZL9r0FTS8_-HmmPQceUjwRZGo7wd3Yc_tTBID74NIyEB5Mv6qQn5oeb8coOuSUfMTcJLFx7OqYkswycayxbYMF7e55dgzU_4oMFvsCXC9PvT2mKUJiGFNaNSktH0ifBhnCIsExOXnO_8xOVxxKt_pCBeCr-XQ15xhkNESJ8mPV7k9T-3qHJhL5RGl1Or-EwK_xK61JhMOTxi6HGWUEVe_tjkLAIKneno2s1xnbUw4Sf1npizjq_45-mMO3_ddUddYHEJ0v0cmfowz2n3a-EIT3zM4dsFA\" rel=\"nofollow noopener\" target=\"_blank\"><strong>https:\/\/clinicaltrials.gov\/ct2\/show\/NCT03412799\u00a0<\/strong><\/a><strong>.<\/strong><\/p>\n<p>\n        <strong>Flynpovi<\/strong><br \/>\n        <strong>\u00a0\u2122<\/strong>\n      <\/p>\n<p>Flynpovi is a combination of CPP-1X (eflornithine) and sulindac with a dual mechanism inhibiting polyamine synthesis and increase polyamine export and catabolism. In a Phase 3 clinical trial in patients with sporadic large bowel polyps, the combination prevented &gt; 90% subsequent pre-cancerous sporadic adenomas versus placebo. Focusing on FAP patients with lower gastrointestinal tract anatomy in the recent Phase 3 trial comparing Flynpovi to single agent eflornithine and single agent sulindac, FAP patients with lower GI anatomy (patients with an intact colon, retained rectum or surgical pouch), Flynpovi showed statistically significant benefit compared to both single agents (p\u22640.02) in delaying surgical events in the lower GI for up to four years. The safety profile for Flynpovi did not significantly differ from the single agents and supports the continued evaluation of Flynpovi for FAP.<\/p>\n<p>\n        <strong>CPP-1X Eflornithine<\/strong>\n      <\/p>\n<p>CPP-1X (eflornithine) is being developed as a single agent tablet or high dose power sachet for several indications including prevention of gastric cancer, treatment of neuroblastoma and recent onset Type 1 diabetes. Preclinical studies as well as Phase 1 or Phase 2 investigator-initiated trials suggest that CPP-1X treatment may be well-tolerated and has potential activity.<\/p>\n<p>\n        <strong>About Panbela<\/strong>\n      <\/p>\n<p>Panbela Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing disruptive therapeutics for patients with urgent unmet medical needs. Panbela\u2019s lead assets are Ivospemin (SBP-101) and Flynpovi. Further information can be found at\u00a0<strong><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=Pdv9FEMcmFCjHhwr6a6tol3gvJSpCeie96MHuBISZylnukRFN5_a0wIe6Vo0r4e8k3zIgjnIQDG1jO6pmy4zmw==\" rel=\"nofollow noopener\" target=\"_blank\">www.panbela.com<\/a>.\u00a0<\/strong>Panbela\u2019s common stock is listed on The Nasdaq Stock Market LLC under the symbol \u201cPBLA\u201d.<\/p>\n<p>\n        <strong>About US <\/strong><br \/>\n        <strong>WorldMeds<\/strong>\n      <\/p>\n<p>US WorldMeds (USWM) is a privately held specialty pharmaceutical company whose treatment options are making a difference in the lives of the patients and communities it serves. USWM takes an agile and personal approach to pharmaceuticals \u2013 pioneering research and product development in therapeutic areas that desperately need new solutions. Headquartered in Louisville, Kentucky, USWM has a global presence and more than 20 years of experience in the development, licensure, and commercialization of unique pharmaceutical products. For more information about USWM, visit <strong>www.usworldmeds.co<\/strong><strong>m<\/strong>.<\/p>\n<p>\n        <strong>Cautionary Statement Regarding Forward-Looking Statements<\/strong>\n      <\/p>\n<p>\n        <em>This\u00a0press\u00a0release contains \u201cforward-looking statements,\u201d including within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as:\u00a0<\/em><br \/>\n        <em>\u201c\u00a0anticipate<\/em><br \/>\n        <em>\u00a0,\u201d\u00a0 \u201cdesign,\u201d \u201cmay,\u201d \u201cplan,\u201d and \u201cwill.\u201d Examples of forward-looking statements include statements we make\u00a0regarding timing of trials and results of collaborations with third parties and future studies. All statements other than statements of historical fact are statements that should be deemed forward-looking statements.\u00a0Forward-looking statements are neither historical facts nor assurances of future performance.\u00a0Instead, they are based only on our current beliefs, expectations, and assumptions regarding the future of our business,\u00a0<\/em><br \/>\n        <em>future plans<\/em><br \/>\n        <em>\u00a0and strategies, projections, anticipated events and trends, the economy and other future conditions. Because forward-looking statements\u00a0relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of our control.\u00a0Our actual results and financial condition may differ materially and adversely from the forward-looking statements.\u00a0Therefore, you should not rely on any of these forward-looking statements.\u00a0Important factors that could cause our actual results and financial condition to differ materially from those indicated in the <\/em><br \/>\n        <em>forward-looking statements include, among others, the following:\u00a0(\u00a0i\u00a0) our ability to obtain additional funding to execute our business and clinical development plans; (ii) progress and success of our clinical development program; (iii) the impact of the current COVID-19 pandemic on our ability to conduct our clinical trials; (iv) our ability to demonstrate the safety and effectiveness of our product candidates:\u00a0ivospemin\u00a0(\u00a0SBP-101\u00a0)\u00a0and eflornithine\u00a0(CPP-1X)\u00a0(v) our reliance on a third party for the execution of the registration trial for our product candidate\u00a0<\/em><br \/>\n        <em>Flynpovi<\/em><br \/>\n        <em>\u00a0; (vi) our ability to obtain regulatory approvals for our product candidates, SBP-101 and\u00a0CPP-1X\u00a0in the United States, the European Union or other international markets; (vii) the market acceptance and level of future sales of our product candidates, SBP-101 and\u00a0CPP-1X\u00a0; (viii) the cost and delays in product development that may result from changes in regulatory oversight applicable to our product candidates, SBP-101 and\u00a0CPP-1X\u00a0; (ix) the rate of progress in establishing reimbursement arrangements with third-party payors; (x) the effect of competing technological and market developments; (xi) the costs involved in filing and prosecuting patent applications and enforcing or defending patent claims;\u00a0and (xii) such other factors as discussed in Part I, Item 1A under the caption \u201cRisk Factors\u201d in our most recent Annual Report on Form 10-K, any additional risks presented in our Quarterly Reports on Form 10-Q and our Current Reports on Form 8-K. Any forward-looking statement made by us in this press release is based on information currently available to us and speaks only as of the date on which it is made.\u00a0We undertake no obligation to publicly update any forward-looking statement or reasons why actual results would differ from those anticipated in any such forward-looking statement,\u00a0whether written or oral, whether\u00a0as\u00a0a result of\u00a0new information, future developments or otherwise.<\/em>\n      <\/p>\n<p>Contact Information:<br \/>Investors:<br \/>James Carbonara<br \/>Hayden IR<br \/>(646) 755-7412<br \/>james@haydenir.com<\/p>\n<p>Media:<br \/>Tammy Groene<br \/>Panbela Therapeutics, Inc.<br \/>(952) 479-1196<br \/>IR@panbela.com<\/p>\n<p>References: <br \/>[1]\u00a0Giselle L. et al.\u00a0Maintenance DFMO Increases Survival in High Risk Neuroblastoma.\u00a0<em>Scientific Reports<\/em>, 2018; 8 (1) DOI:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=0xvJobIt7yOjPrgF70WRSBoYrIcvmxv41p7v-0aQCYUU3dMrvhfO7imebppoWFxGhSY-Efa7T3qCED-c4DiTnMfxXwa-8cY_OstXmbdCAGLuN_Ntg5Tdoh4Rio7kaDVA\" rel=\"nofollow noopener\" target=\"_blank\">10.1038\/s41598-018-32659-w<\/a><\/p>\n<p>\u00a0\u00a0<\/p>\n<hr \/>\n<p>\n        <sup>1<\/sup> US WORLDMEDS is a registered trademark of USWM, LLC.<\/p>\n<\/p>\n<p>      <img decoding=\"async\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODg3Njc0NCM1Njk4Mjk2IzIwMjgxMTk=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" src=\"https:\/\/ml.globenewswire.com\/media\/NTZmMjE2NjEtZjhjOC00ZGIxLTgzZmEtODY1Yzk1MGE1MWUxLTEwMzkzNjI=\/tiny\/Panbela-Therapeutics-Inc-.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>MINNEAPOLIS and LOUISVILLE, Ky., July 19, 2023 (GLOBE NEWSWIRE) &#8212; Panbela Therapeutics, Inc. (Nasdaq: PBLA), a clinical stage company developing disruptive therapeutics for the treatment of patients with urgent unmet medical needs, today announced it has divested certain assets in its eflornithine pediatric neuroblastoma program to US WorldMeds\u00ae1 (USWM), a Kentucky-based specialty pharmaceutical company. Neuroblastoma, a rare cancer originating from immature nerve cells, contributes to nearly 15% of pediatric cancer deaths.[1] Panbela Therapeutics&#8217; subsidiary, Cancer Prevention Pharmaceuticals, has extensively collaborated with leading neuroblastoma research groups such as the Neuroblastoma Medulloblastoma Translational Research Consortium (NMTRC) (now Beat Childhood Cancer), New Advances in Neuroblastoma Therapy (NANT), the Children\u2019s Oncology Group (COG), and the National Cancer Institute (NCI) in the clinical development of &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds&#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-770910","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds - 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\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"MINNEAPOLIS and LOUISVILLE, Ky., July 19, 2023 (GLOBE NEWSWIRE) &#8212; Panbela Therapeutics, Inc. (Nasdaq: PBLA), a clinical stage company developing disruptive therapeutics for the treatment of patients with urgent unmet medical needs, today announced it has divested certain assets in its eflornithine pediatric neuroblastoma program to US WorldMeds\u00ae1 (USWM), a Kentucky-based specialty pharmaceutical company. Neuroblastoma, a rare cancer originating from immature nerve cells, contributes to nearly 15% of pediatric cancer deaths.[1] Panbela Therapeutics&#8217; subsidiary, Cancer Prevention Pharmaceuticals, has extensively collaborated with leading neuroblastoma research groups such as the Neuroblastoma Medulloblastoma Translational Research Consortium (NMTRC) (now Beat Childhood Cancer), New Advances in Neuroblastoma Therapy (NANT), the Children\u2019s Oncology Group (COG), and the National Cancer Institute (NCI) in the clinical development of &hellip; Continue reading &quot;Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2023-07-19T14:26:12+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODg3Njc0NCM1Njk4Mjk2IzIwMjgxMTk=\" \/>\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\\\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds\",\"datePublished\":\"2023-07-19T14:26:12+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\\\/\"},\"wordCount\":1596,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=ODg3Njc0NCM1Njk4Mjk2IzIwMjgxMTk=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\\\/\",\"name\":\"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds - 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Neuroblastoma, a rare cancer originating from immature nerve cells, contributes to nearly 15% of pediatric cancer deaths.[1] Panbela Therapeutics&#8217; subsidiary, Cancer Prevention Pharmaceuticals, has extensively collaborated with leading neuroblastoma research groups such as the Neuroblastoma Medulloblastoma Translational Research Consortium (NMTRC) (now Beat Childhood Cancer), New Advances in Neuroblastoma Therapy (NANT), the Children\u2019s Oncology Group (COG), and the National Cancer Institute (NCI) in the clinical development of &hellip; Continue reading \"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/","og_site_name":"Market Newsdesk","article_published_time":"2023-07-19T14:26:12+00:00","og_image":[{"url":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODg3Njc0NCM1Njk4Mjk2IzIwMjgxMTk=","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"8 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds","datePublished":"2023-07-19T14:26:12+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/"},"wordCount":1596,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODg3Njc0NCM1Njk4Mjk2IzIwMjgxMTk=","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/panbela-therapeutics-to-receive-a-total-up-to-9-5-million-for-divestiture-of-assets-within-eflornithine-dfmo-pediatric-neuroblastoma-program-to-us-worldmeds\/","name":"Panbela Therapeutics to Receive a Total Up to $9.5 Million for Divestiture of Assets within Eflornithine (DFMO) Pediatric Neuroblastoma Program to US WorldMeds - 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