Monopar Announces MNPR-101-RIT Abstract Accepted as a Top-Rated Oral Presentation at EANM'24
Monopar Announces MNPR-101-RIT Abstract Accepted as a Top-Rated Oral Presentation at EANM'24
WILMETTE, Ill., June 25, 2024 (GLOBE NEWSWIRE) -- Monopar Therapeutics Inc. (Nasdaq: MNPR), a clinical-stage radiopharma company focused on developing innovative treatments for cancer patients, today announced that its abstract titled "Evaluation of Anti-uPAR Antibody as a Radiopharmaceutical for Imaging and Treatment of Solid Tumors" has been accepted as a "Top-Rated Oral Presentation" within the Scientific Program of the European Association of Nuclear Medicine (EANM) 2024 Annual Congress to be held on October 19-23, 2024 in Hamburg, Germany.
今天,2024年6月25日,伊利諾伊州威爾梅特(WILMETTE),臨床階段放射藥物公司monopar therapeutics(Nasdaq:MNPR)宣佈,其題爲“評估抗uPAR抗體作爲實體腫瘤成像和治療的放射藥物”的摘要已被歐洲核醫學協會(EANM)2024年年會的科學方案中接受爲“最佳口頭報告”。該年會將於2024年10月19日至23日在德國漢堡舉行。
Monopar's abstract details its MNPR-101-RIT, a novel first-in-class radio-immuno-therapeutic program that targets cancers expressing the urokinase plasminogen activator receptor (uPAR), including triple-negative breast, colorectal, and pancreatic cancers. The Company's preclinical data demonstrate compelling and durable anti-tumor benefits with MNPR-101 conjugated to therapeutic radioisotopes, including lutetium-177 (Lu-177) and actinium-225 (Ac-225).
monopar的摘要詳細介紹了其MNPR-101-RIT,一項新穎的第一類放射免疫治療計劃,該計劃針對表達泌尿激酶型纖溶酶原激活劑受體(uPAR)的癌症,包括三陰性乳腺癌,結直腸癌和胰腺癌。該公司的臨床前數據表明,MNPR-101偶聯到治療性放射性同位素,包括鑥-177(Lu-177)和錒-225(Ac-225),具有令人信服且持久的抗腫瘤效益。
"We are honored by the recognition of our MNPR-101-RIT abstract at EANM'24," said Chandler Robinson, MD, CEO of Monopar Therapeutics. "This selection underscores the potential of our uPAR-targeted therapy and the interest around uPAR as a potential new target for radiopharma treatment."
“我們很榮幸在EANM24上得到MNPR-101-RIT摘要的認可,”monopar therapeutics的CEO Chandler Robinson博士說。“此次選擇突顯了我們uPAR靶向治療的潛力以及uPAR作爲放射藥物治療潛在新靶點的興趣。”
Monopar recently initiated its MNPR-101-Zr first-in-human Phase 1 imaging and dosimetry clinical trial in advanced cancer patients. Further information about this trial is available at under study identifier NCT06337084.
monopar最近在先進癌症患者中啓動了MNPR-101-Zr先人成像和劑量測定的一期臨床試驗。有關該試驗的更多信息,請訪問org,並查看研究標識符NCT06337084。
About Monopar Therapeutics Inc.
關於Monopar Therapeutics Inc。
Monopar Therapeutics is a clinical-stage radiopharmaceutical company focused on developing innovative treatments for cancer patients, including Phase 1-stage MNPR-101-Zr for imaging advanced cancers and late preclinical-stage MNPR-101 radio-immuno-therapeutic (RIT) for the treatment of advanced cancers, as well as early development programs against solid cancers. For more information, visit: .
Monopar Therapeutics是一家致力於爲癌症患者開發創新治療方法的臨床階段放射藥物公司,包括用於成像高級癌症的一階段MNPR-101-Zr和用於治療高級癌症和晚期臨床前階段MNPR-101放射免疫治療(RIT),以及用於實體癌的早期開發計劃。有關更多信息,請訪問。
Forward-Looking Statements
前瞻性聲明
Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. The words "may," "will," "could," "would," "should," "expect," "plan," "anticipate," "intend," "believe," "estimate," "predict," "project," "potential," "continue," "target" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Examples of these forward-looking statements include statements concerning: the Company's preclinical data demonstrating compelling and durable anti-tumor benefits with MNPR-101 conjugated to therapeutic radioisotopes, including lutetium-177 (Lu-177) and actinium-225 (Ac-225); and that the selection of Monopar's abstract underscores the potential of its uPAR-targeted therapy and the interest around uPAR as a potential new target for radiopharma treatment. The forward-looking statements involve risks and uncertainties including, but not limited to: the recently initiated first-in-human Phase 1 imaging and dosimetry clinical trial in advanced cancer patients with MNPR-101-Zr may not yield satisfactory results, if at all; that future preclinical or clinical data will not be as promising as the data to date; not receiving regulatory clearance to proceed into human clinical trials for MNPR-101-RIT; that MNPR-101-Zr and/or MNPR-101-RIT may cause unexpected serious adverse effects in humans; and the significant general risks and uncertainties surrounding the research, development, regulatory approval, and commercialization of imaging agents and therapeutics. Actual results may differ materially from those expressed or implied by such forward-looking statements. Risks are described more fully in Monopar's filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made. Monopar undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made. Any forward-looking statements contained in this press release represent Monopar's views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date.
本新聞稿中的包含關於非歷史事實的陳述的“前瞻性陳述”涉及風險和不確定性,儘管並非所有前瞻性陳述都包含這些識別字。這些前瞻性陳述的例子包括關於:MNPR-101偶聯到治療性放射性同位素,包括鑥-177(Lu-177)和錒-225(Ac-225),該公司的臨床前數據表明具有令人信服且持久的抗腫瘤效益;以及monopar摘要的選擇突顯了其uPAR靶向治療的潛力以及uPAR作爲放射藥物治療潛在新靶點的興趣。上述前瞻性陳述包含風險和不確定性,包括但不限於:用MNPR-101-Zr在先進癌症患者中最近啓動的第一期成像和劑量測定臨床試驗可能根本不會產生令人滿意的結果;未來的臨床前或臨床數據將不像迄今的數據那麼有前途;未獲得批准進行MNPR-101-RIT的人體臨床試驗;MNPR-101-Zr和/或MNPR-101-RIT可能在人體中引起意外嚴重副作用;以及圍繞成像劑和治療劑研究,開發,獲得監管批准和商業化的普遍重大風險和不確定性。事實結果可能與此類前瞻性陳述所表達的不同。更全面的風險在monopar提交給證券交易委員會的文件中進行了描述。本新聞稿中包含的所有前瞻性陳述僅於其發表日期說明。monopar對於更新這些陳述以反映發生的事件或存在的情況不承擔任何義務。本新聞稿中包含的任何前瞻性陳述僅代表monopar當天的觀點,不應被依賴作爲其任何後續日期觀點的代表。
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Monopar Therapeutics Inc.
投資者關係
Kim R. Tsuchimoto
Chief Financial Officer
kimtsu@monopartx.com
Kim R. Tsuchimoto
致富金融(臨時代碼)
kimtsu@monopartx.com
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